• Carmen Leitch - A Mysterious Plasmid is Found at High Levels in the Human Gut:

    https://www.labroots.com/trending/genetics-and-genomics/27029/mysterious-plasmid-found-levels-human-gut

    #Plasmid #PBI143 #Metagenome #Gastrointestinal #Gut #Microbiology #Biology
    Carmen Leitch - A Mysterious Plasmid is Found at High Levels in the Human Gut: https://www.labroots.com/trending/genetics-and-genomics/27029/mysterious-plasmid-found-levels-human-gut #Plasmid #PBI143 #Metagenome #Gastrointestinal #Gut #Microbiology #Biology
    WWW.LABROOTS.COM
    A Mysterious Plasmid is Found at High Levels in the Human Gut | Genetics And Genomics
    There are trillions of microorganisms in the human gastrointestinal tract, and this gut microbiome includes bacteria, archaea, viruses, and fungi. | Genetics And Genomics
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  • Eminent French Geneticist Dr. Alexandra Henrion-Caude, and Top Investigative Reporter Corinne Lalo Expose the mRNA Vaccine Risks and WHO's Controversial Pandemic Power Grab

    "mRNA vaccines are GMOs. And European law was changed in 2020 to be able to allow the arrival of vaccines GMOs, which are mRNA vaccines,"

    "Recently, Kevin McKernan showed that in vaccines, there was not only mRNA but there was also DNA... up to 30%…So that means that if we find DNA in vaccines, it will end up in genomes,"

    https://vk.com/video-177757343_456244085?access_key=1cc4a41e015243b2cf
    Eminent French Geneticist Dr. Alexandra Henrion-Caude, and Top Investigative Reporter Corinne Lalo Expose the mRNA Vaccine Risks and WHO's Controversial Pandemic Power Grab "mRNA vaccines are GMOs. And European law was changed in 2020 to be able to allow the arrival of vaccines GMOs, which are mRNA vaccines," "Recently, Kevin McKernan showed that in vaccines, there was not only mRNA but there was also DNA... up to 30%…So that means that if we find DNA in vaccines, it will end up in genomes," https://vk.com/video-177757343_456244085?access_key=1cc4a41e015243b2cf
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  • More Proof mRNA Shots Edit Human Genome
    New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work

    Dr. Syed Haider
    Could the mRNA shots edit germline DNA?
    Honest scientists have always been worried about retrointegration of foreign mRNA from “vaccine” shots into our own cellular DNA.

    This fear should have been allayed by rigorous genotoxicity safety studies before the mRNA shots where rolled out, but those studies were waived by the Big Pharma controlled FDA (with the DoD behind the scenes pulling all the strings).

    Previous research showed that this could theoretically occur in a human liver cancer cell line inside a controlled laboratory setting utilizing our own bodies reverse transcriptase enzymes that are upregulated in cancer cells.

    Naysayers still argued that this situation was impossible or at least extremely unlikely to occur in our bodies.

    Unfortunately there is now further proof that this really does occur, either right away after vaccination, or if not, then it’s even more likely to occur once a vaccinated individual catches COVID-19, as long as vaccinal mRNA remains present in the body (so far we know it remains in circulation for weeks and in the lymph nodes for months - likely far longer, since all the studies had to be stopped, presumably due to lack of funding, or out of fear of creating unpublishable papers since the news wasn’t looking good).

    Thank you for reading Dr. Syed Haider. This post is public so feel free to share it.

    Share

    A new paper by Zhang et al, just released on Feb 13, 2023 proves that at artificially high concentrations in a lab setting, the SARS-CoV-2 virus can retrointegrate into our genome.

    Thankfully during natural infection such high levels of viral RNA do not typically occur, but … (you knew there had to be a “but”)

    … such high levels are induced by mRNA vaccination.

    So what the paper may actually prove in the roundabout way of most modern research (required for publication to ever happen in todays politically charged Big Pharma controlled publishing environment) is that the mRNA in the shots is in fact likely to retrointegrate into our cellular DNA.

    To dig into the details we need to start with a quick basic bio refresher:

    Understanding Genetics
    Nearly every cell in our bodies carries a full copy of our genetic code, or genome (the exceptions are red blood cells that have no genome, and sperm and egg cells that have half a genome since they are meant to combine with half of someone else's genome).

    Our genome is made up of individual genes encoded by DNA and bundled together into 46 chromosomes that are stored in a central compartment of our cells called the nucleus.

    In order to “read" the DNA code and convert it into the structure that makes up our bodies, it is first translated by a “reader” protein that writes it out into a new free floating molecule called mRNA for messenger RNA (the mRNA shots carry this messenger RNA, not modified RNA as some people think).

    The mRNA, unlike the DNA is not stuck inside the chromosome and it can exit the nucleus, going into the larger compartment called the cytoplasm of the cell, where its message is “read” and translated into an amino acid sequence that folds itself into a protein (either a body protein, or in the case of the shots the spike protein, or in the case of an RNA virus infection like SARS-CoV-2, all the proteins of the virus).

    Now going back to the nucleus: some of the individual DNA encoded genes can move around within their chromosomes and have therefore been described as "jumping genes" or technically speaking: transposable elements (TEs).

    Jumping genes!
    Some of these jumping genes (Class 1 TEs) use a copy and paste mechanism and others (Class 2 TEs), like the one in the cartoon depiction above, use a cut and paste mechanism.

    The Class 1 TEs (AKA retrotransposons) that use the copy and paste mechanism do so by translating their DNA into RNA and then converting the RNA back into DNA and inserting it somewhere else in the genome.

    The Class 1 TEs or retrotransposons, include within themselves the genetic code necessary to create their own protein enzyme to convert the DNA back into RNA, which is termed reverse transcriptase.

    Fun fact: retroviruses like HIV can be considered a special subtype of retrotransposon that can not only reinsert inside the same cell, but also travel to other cells “infecting” them and reverse transcribing into their genomes.

    In humans the only active jumping genes are from CLASS 1 TEs/retrotransposons and are called LINE-1 retrotransposons (LINE stands for Long Interspersed Nuclear Elements).

    LINE-1 retrotransposons were once considered to be junk DNA, they are usually inactivated, but can be turned on in aging cells, cancer cells, virus infected cells and in general in any cell subjected to significant stress.

    Junk DNA, which makes up 98.5% of our genome, is still little understood. It may help regulate the activity of the other 1.5% of the genome that does code for proteins, is likely involved in genome evolution, and has been implicated in disease states like cancer, autism and dozens of genetic diseases.

    So, what’s been shown in this new paper by Zhang et al, is that a lab clone of the SARS-CoV-2 virus, when present in very high levels, does turn on LINE-1, which means it also turns on the LINE-1 reverse transcriptase enzyme, which it then makes use of to reverse transcribe itself into our DNA.

    But even worse: genome sequencing found the viral genetic code transcribed into our DNA not only in cells where LINE-1 was actively turned on, or overexpressed above baseline, but even in cells where it was not.

    Is Sangamo's Gene-Editing Approach a Bust? | The Motley Fool
    Then, instead of studying the LNPs and spike protein RNA used in the shots, the researchers (who valued their careers) used a different mechanism of delivering low levels of nucleocapsid RNA into the cells in the lab to see if they also up regulated LINE-1 expression and were integrated into the cellular DNA.

    Turns out this handicapped experiment did not up regulate LINE-1, or get taken up in detectable quantities by healthy cells, though it did lead to genomic uptake in cells that already had LINE-1 upregulated - which again happens in aging cells, cancer cells, virus infected cells or simply in cells under stress (perhaps from LNP and spike protein induced inflammation?).

    The study authors addressed the discrepancy in retrointegration between the viral clone and their handicapped version of an mRNA shot by theorizing there were:

    "...several possible explanations for the differences in the levels of retrotransposition in infected and transfected cells: (i) The relative abundance of viral RNA is almost 2 orders of magnitude higher in infected than in transfected cells which would increase the probability of association with LINE1 proteins; (ii) virus infection, but not viral mRNA transfection, can induce endogenous LINE1 expression; (iii) multiple factors during SARS-CoV-2 infection can inhibit the antiviral/anti-retrotransposition function of stress granules (48–53), which could increase retrotransposition.”

    The first theory is the most concerning.

    Based on what we know from a 2020 study by Xie et al that showed the very high levels of intracellular viral RNA achieved by infectious clones, we can extrapolate that in the current study by Zhang et al the concentration of mRNA achieved by the SARS-CoV-2 viral clone was likely about 1000X greater than the low levels typically found during a natural infection.

    In fact the levels of mRNA in each cell achieved by the viral clone in the current study are actually far more likely to be achieved by transfection into cells of LNPs in the shots carrying spike protein mRNA than they are during a natural infection.

    Life finds a way. - Reaction GIFs
    So if the authors first theory is correct, that the difference in retrointegration rates simply depends on the intracellular concentration of foreign RNA, then retrointegration is very likely to occur due to exposure to mRNA in the shots, and it is likely to dramatically increase in case someone who has received the shot later becomes infected by the SARS-CoV-2 virus - since we know it upregulates LINE-1 expression, or if they are put under other stressors including the development of cancer, or by the stress of long COVID, chronic vaccine injury, autoimmune disease, autonomic dysfunction, POTS, MCAS, etc - all of which are also sadly enough triggered by the shot.

    This is less likely to happen in germ cell DNA - our sperm and egg cells - and lets hope it doesn’t happen, since we already know that the shots likely do transmit altered immunity from mother to child, if they also pass on the mRNA coding the spike protein itself then huge swaths of humanity may be forever genetically altered.

    Heres hoping the label “junk DNA” actually applies in this case…

    But, if you’ve been vaccinated: don’t worry!

    At mygotodoc we routinely reverse vaccine injuries and sincerely believe every disease has a cure.

    Fear is more likely to kill you than the shot (but do stop getting the boosters), and I mean that literally: fear destroys the immune system.

    A healthy immune system can keep any illness in check even if from a retrointegrated virus or viral mRNA fragment.

    There are a lot of unknowns, but don’t let that scare you. Take your health into your own hands and start making positive changes today.

    https://blog.mygotodoc.com/p/more-proof-mrna-shots-edit-human


    https://telegra.ph/More-Proof-mRNA-Shots-Edit-Human-Genome-09-17-2
    More Proof mRNA Shots Edit Human Genome New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work Dr. Syed Haider Could the mRNA shots edit germline DNA? Honest scientists have always been worried about retrointegration of foreign mRNA from “vaccine” shots into our own cellular DNA. This fear should have been allayed by rigorous genotoxicity safety studies before the mRNA shots where rolled out, but those studies were waived by the Big Pharma controlled FDA (with the DoD behind the scenes pulling all the strings). Previous research showed that this could theoretically occur in a human liver cancer cell line inside a controlled laboratory setting utilizing our own bodies reverse transcriptase enzymes that are upregulated in cancer cells. Naysayers still argued that this situation was impossible or at least extremely unlikely to occur in our bodies. Unfortunately there is now further proof that this really does occur, either right away after vaccination, or if not, then it’s even more likely to occur once a vaccinated individual catches COVID-19, as long as vaccinal mRNA remains present in the body (so far we know it remains in circulation for weeks and in the lymph nodes for months - likely far longer, since all the studies had to be stopped, presumably due to lack of funding, or out of fear of creating unpublishable papers since the news wasn’t looking good). Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share A new paper by Zhang et al, just released on Feb 13, 2023 proves that at artificially high concentrations in a lab setting, the SARS-CoV-2 virus can retrointegrate into our genome. Thankfully during natural infection such high levels of viral RNA do not typically occur, but … (you knew there had to be a “but”) … such high levels are induced by mRNA vaccination. So what the paper may actually prove in the roundabout way of most modern research (required for publication to ever happen in todays politically charged Big Pharma controlled publishing environment) is that the mRNA in the shots is in fact likely to retrointegrate into our cellular DNA. To dig into the details we need to start with a quick basic bio refresher: Understanding Genetics Nearly every cell in our bodies carries a full copy of our genetic code, or genome (the exceptions are red blood cells that have no genome, and sperm and egg cells that have half a genome since they are meant to combine with half of someone else's genome). Our genome is made up of individual genes encoded by DNA and bundled together into 46 chromosomes that are stored in a central compartment of our cells called the nucleus. In order to “read" the DNA code and convert it into the structure that makes up our bodies, it is first translated by a “reader” protein that writes it out into a new free floating molecule called mRNA for messenger RNA (the mRNA shots carry this messenger RNA, not modified RNA as some people think). The mRNA, unlike the DNA is not stuck inside the chromosome and it can exit the nucleus, going into the larger compartment called the cytoplasm of the cell, where its message is “read” and translated into an amino acid sequence that folds itself into a protein (either a body protein, or in the case of the shots the spike protein, or in the case of an RNA virus infection like SARS-CoV-2, all the proteins of the virus). Now going back to the nucleus: some of the individual DNA encoded genes can move around within their chromosomes and have therefore been described as "jumping genes" or technically speaking: transposable elements (TEs). Jumping genes! Some of these jumping genes (Class 1 TEs) use a copy and paste mechanism and others (Class 2 TEs), like the one in the cartoon depiction above, use a cut and paste mechanism. The Class 1 TEs (AKA retrotransposons) that use the copy and paste mechanism do so by translating their DNA into RNA and then converting the RNA back into DNA and inserting it somewhere else in the genome. The Class 1 TEs or retrotransposons, include within themselves the genetic code necessary to create their own protein enzyme to convert the DNA back into RNA, which is termed reverse transcriptase. Fun fact: retroviruses like HIV can be considered a special subtype of retrotransposon that can not only reinsert inside the same cell, but also travel to other cells “infecting” them and reverse transcribing into their genomes. In humans the only active jumping genes are from CLASS 1 TEs/retrotransposons and are called LINE-1 retrotransposons (LINE stands for Long Interspersed Nuclear Elements). LINE-1 retrotransposons were once considered to be junk DNA, they are usually inactivated, but can be turned on in aging cells, cancer cells, virus infected cells and in general in any cell subjected to significant stress. Junk DNA, which makes up 98.5% of our genome, is still little understood. It may help regulate the activity of the other 1.5% of the genome that does code for proteins, is likely involved in genome evolution, and has been implicated in disease states like cancer, autism and dozens of genetic diseases. So, what’s been shown in this new paper by Zhang et al, is that a lab clone of the SARS-CoV-2 virus, when present in very high levels, does turn on LINE-1, which means it also turns on the LINE-1 reverse transcriptase enzyme, which it then makes use of to reverse transcribe itself into our DNA. But even worse: genome sequencing found the viral genetic code transcribed into our DNA not only in cells where LINE-1 was actively turned on, or overexpressed above baseline, but even in cells where it was not. Is Sangamo's Gene-Editing Approach a Bust? | The Motley Fool Then, instead of studying the LNPs and spike protein RNA used in the shots, the researchers (who valued their careers) used a different mechanism of delivering low levels of nucleocapsid RNA into the cells in the lab to see if they also up regulated LINE-1 expression and were integrated into the cellular DNA. Turns out this handicapped experiment did not up regulate LINE-1, or get taken up in detectable quantities by healthy cells, though it did lead to genomic uptake in cells that already had LINE-1 upregulated - which again happens in aging cells, cancer cells, virus infected cells or simply in cells under stress (perhaps from LNP and spike protein induced inflammation?). The study authors addressed the discrepancy in retrointegration between the viral clone and their handicapped version of an mRNA shot by theorizing there were: "...several possible explanations for the differences in the levels of retrotransposition in infected and transfected cells: (i) The relative abundance of viral RNA is almost 2 orders of magnitude higher in infected than in transfected cells which would increase the probability of association with LINE1 proteins; (ii) virus infection, but not viral mRNA transfection, can induce endogenous LINE1 expression; (iii) multiple factors during SARS-CoV-2 infection can inhibit the antiviral/anti-retrotransposition function of stress granules (48–53), which could increase retrotransposition.” The first theory is the most concerning. Based on what we know from a 2020 study by Xie et al that showed the very high levels of intracellular viral RNA achieved by infectious clones, we can extrapolate that in the current study by Zhang et al the concentration of mRNA achieved by the SARS-CoV-2 viral clone was likely about 1000X greater than the low levels typically found during a natural infection. In fact the levels of mRNA in each cell achieved by the viral clone in the current study are actually far more likely to be achieved by transfection into cells of LNPs in the shots carrying spike protein mRNA than they are during a natural infection. Life finds a way. - Reaction GIFs So if the authors first theory is correct, that the difference in retrointegration rates simply depends on the intracellular concentration of foreign RNA, then retrointegration is very likely to occur due to exposure to mRNA in the shots, and it is likely to dramatically increase in case someone who has received the shot later becomes infected by the SARS-CoV-2 virus - since we know it upregulates LINE-1 expression, or if they are put under other stressors including the development of cancer, or by the stress of long COVID, chronic vaccine injury, autoimmune disease, autonomic dysfunction, POTS, MCAS, etc - all of which are also sadly enough triggered by the shot. This is less likely to happen in germ cell DNA - our sperm and egg cells - and lets hope it doesn’t happen, since we already know that the shots likely do transmit altered immunity from mother to child, if they also pass on the mRNA coding the spike protein itself then huge swaths of humanity may be forever genetically altered. Heres hoping the label “junk DNA” actually applies in this case… But, if you’ve been vaccinated: don’t worry! At mygotodoc we routinely reverse vaccine injuries and sincerely believe every disease has a cure. Fear is more likely to kill you than the shot (but do stop getting the boosters), and I mean that literally: fear destroys the immune system. A healthy immune system can keep any illness in check even if from a retrointegrated virus or viral mRNA fragment. There are a lot of unknowns, but don’t let that scare you. Take your health into your own hands and start making positive changes today. https://blog.mygotodoc.com/p/more-proof-mrna-shots-edit-human https://telegra.ph/More-Proof-mRNA-Shots-Edit-Human-Genome-09-17-2
    BLOG.MYGOTODOC.COM
    More Proof mRNA Shots Edit Human Genome
    New Study Again Shows LINE-1 "Junk DNA" Does The Dirty Work
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  • SV40, a DNA Altering, Carcinogenic Contaminant, found in Pfizer’s COVID-19 Vaccines
    The ExposéMarch 17, 2024
    It’s not just the spike protein and the mRNA that are a problem. Both Pfizer and Moderna covid injections also have DNA contamination and Pfizer’s covid injection contains SV40 promoters.

    Microbiologist Kevin McKernan pioneered research on testing some of the covid vaccine vials and discovered unacceptable levels of double-stranded DNA plasmids floating around. This is DNA contamination. He found the contamination in Pfizer and Moderna vials.

    During an interview with Peter Sweden, Sasha Latypova said that DNA contamination is “a huge problem because this is replication competent plasmid, it can then invade human cells, it can invade the bacterial cells that live in your gut. So, they go into the bacteria they replicate there, they replicate antibiotic-resistant genes…it can cause sepsis, it can cause cancer, all sorts of issues.”

    The World Council for Health (“WCH”) stated that a red line has been crossed. “DNA contamination of mRNA ‘vaccines’ poses a risk to everyone on the planet,” WCH said. “Replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all … We can only speculate how it will end, but what needs to happen today after the publication of the paper by McKernan et al (2023) is an immediate stop of the ‘covid-19 vaccine’ program.”

    In Pfizer’s mRNA injection, McKernan also discovered Simian Virus 40 (“SV40”) promoters which are tied to cancer development in humans. He emphasised that the SV40 found is a viral piece, it is not the whole virus. However, it still presents a risk of driving cancer.

    SV40 or Simian Virus 40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This virus contaminated both the inactivated polio vaccine (“IPV”) and the oral or “live” polio vaccine (“OPV”) developed by Dr. Albert Sabin. When it was discovered that SV40 was an animal carcinogen that had found its way into the polio vaccines, a federal law was passed in 1961 that required that no vaccines contain this virus.

    Kanekoa The Great tweeted two audio/video transcripts. One of a recent interview with McKernan explaining his discoveries and another of a Japanese professor expressing his concerns about these discoveries. We have republished these transcripts below.

    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    DNA Contamination and SV40 Discovered

    McKernan joined Conservative Review with Daniel Horowitz on Friday to warn that there is no quality control in the manufacturing process of these vaccines. If his findings turn out to be widespread, it could portend an even greater risk for anaphylaxis, blood clotting, developing resistance to antibiotics, gene integration risk, and long-term production of spike protein within the body. You can listen to an audio of the interview on Apple podcasts HERE.

    During the interview, McKernan said:

    “It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination. If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA…

    “Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected. And, of course, your viewers and listeners are probably aware there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA…

    “At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression. And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA is that these things can then integrate into the genome. If you’re not careful with how you manufacture these things, and you have excess amounts of this DNA, your concern for genome integration goes up…

    “If you get an SV40 promoter in front of an oncogene, you will end up with a high expression of a gene that can drive cancer, it will be a very rare event, but you don’t need many of these cells to be hit with something like this for it to take off. SV40 actually plagued, granted it was the full viral genome, not just the promoter, but this has plagued previous vaccine programs. The polio vaccine is one of them that they were concerned that this may have contributed to cancer from that vaccine. So, there’s a history of being concerned over SV40.

    “Having the promoter inside some of these vectors isn’t necessary. It seems to be superfluous oversight they could have eliminated, yet it’s still there because they ran this out the door so quickly, they didn’t really have time to get rid of superfluous parts of the plasmid. So, that piece of DNA is something we really need to pay attention to. We’ve made quantitative PCR assays to hunt for this. So several researchers around the globe are now running these assays to look for how much of this DNA is floating around after people have been vaccinated.”

    Further reading:

    Sequencing the Pfizer monovalent mRNA vaccines also reveals dual copy 72-bp SV40 Promoter, Anandamide (Kevin McKernan), 12 April 2023
    dsDNA variance in Pfizer Docs, Anandamide (Kevin McKernan), 20 May 2023
    McKernan, K., Helbert, Y., Kane, L. T., & McLaughlin, S. (2023, April 10). Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose. https://doi.org/10.31219/osf.io/b9t7m
    Plasmid DNA is a Known Pfizer Ingredient – NOT a Contaminant, Karen Kingston, 14 April 2023
    Japanese Professor Expresses Concern

    Japanese Professor Murakami of Tokyo University expressed his concerns over the alarming discovery of SV40 promoters McKernan had made. He said:

    “The Pfizer vaccine has a staggering problem. I have made an amazing finding. This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter. Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus.

    “The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine. There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine. This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus.

    “So, it means that the DNA can easily enter the genome. This is such an alarming problem. It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”


    https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-vaccines/
    SV40, a DNA Altering, Carcinogenic Contaminant, found in Pfizer’s COVID-19 Vaccines The ExposéMarch 17, 2024 It’s not just the spike protein and the mRNA that are a problem. Both Pfizer and Moderna covid injections also have DNA contamination and Pfizer’s covid injection contains SV40 promoters. Microbiologist Kevin McKernan pioneered research on testing some of the covid vaccine vials and discovered unacceptable levels of double-stranded DNA plasmids floating around. This is DNA contamination. He found the contamination in Pfizer and Moderna vials. During an interview with Peter Sweden, Sasha Latypova said that DNA contamination is “a huge problem because this is replication competent plasmid, it can then invade human cells, it can invade the bacterial cells that live in your gut. So, they go into the bacteria they replicate there, they replicate antibiotic-resistant genes…it can cause sepsis, it can cause cancer, all sorts of issues.” The World Council for Health (“WCH”) stated that a red line has been crossed. “DNA contamination of mRNA ‘vaccines’ poses a risk to everyone on the planet,” WCH said. “Replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all … We can only speculate how it will end, but what needs to happen today after the publication of the paper by McKernan et al (2023) is an immediate stop of the ‘covid-19 vaccine’ program.” In Pfizer’s mRNA injection, McKernan also discovered Simian Virus 40 (“SV40”) promoters which are tied to cancer development in humans. He emphasised that the SV40 found is a viral piece, it is not the whole virus. However, it still presents a risk of driving cancer. SV40 or Simian Virus 40 was the 40th virus found in rhesus monkey kidney cells when these cells were used to make the polio vaccine. This virus contaminated both the inactivated polio vaccine (“IPV”) and the oral or “live” polio vaccine (“OPV”) developed by Dr. Albert Sabin. When it was discovered that SV40 was an animal carcinogen that had found its way into the polio vaccines, a federal law was passed in 1961 that required that no vaccines contain this virus. Kanekoa The Great tweeted two audio/video transcripts. One of a recent interview with McKernan explaining his discoveries and another of a Japanese professor expressing his concerns about these discoveries. We have republished these transcripts below. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… DNA Contamination and SV40 Discovered McKernan joined Conservative Review with Daniel Horowitz on Friday to warn that there is no quality control in the manufacturing process of these vaccines. If his findings turn out to be widespread, it could portend an even greater risk for anaphylaxis, blood clotting, developing resistance to antibiotics, gene integration risk, and long-term production of spike protein within the body. You can listen to an audio of the interview on Apple podcasts HERE. During the interview, McKernan said: “It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination. If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA… “Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected. And, of course, your viewers and listeners are probably aware there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA… “At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression. And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA is that these things can then integrate into the genome. If you’re not careful with how you manufacture these things, and you have excess amounts of this DNA, your concern for genome integration goes up… “If you get an SV40 promoter in front of an oncogene, you will end up with a high expression of a gene that can drive cancer, it will be a very rare event, but you don’t need many of these cells to be hit with something like this for it to take off. SV40 actually plagued, granted it was the full viral genome, not just the promoter, but this has plagued previous vaccine programs. The polio vaccine is one of them that they were concerned that this may have contributed to cancer from that vaccine. So, there’s a history of being concerned over SV40. “Having the promoter inside some of these vectors isn’t necessary. It seems to be superfluous oversight they could have eliminated, yet it’s still there because they ran this out the door so quickly, they didn’t really have time to get rid of superfluous parts of the plasmid. So, that piece of DNA is something we really need to pay attention to. We’ve made quantitative PCR assays to hunt for this. So several researchers around the globe are now running these assays to look for how much of this DNA is floating around after people have been vaccinated.” Further reading: Sequencing the Pfizer monovalent mRNA vaccines also reveals dual copy 72-bp SV40 Promoter, Anandamide (Kevin McKernan), 12 April 2023 dsDNA variance in Pfizer Docs, Anandamide (Kevin McKernan), 20 May 2023 McKernan, K., Helbert, Y., Kane, L. T., & McLaughlin, S. (2023, April 10). Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose. https://doi.org/10.31219/osf.io/b9t7m Plasmid DNA is a Known Pfizer Ingredient – NOT a Contaminant, Karen Kingston, 14 April 2023 Japanese Professor Expresses Concern Japanese Professor Murakami of Tokyo University expressed his concerns over the alarming discovery of SV40 promoters McKernan had made. He said: “The Pfizer vaccine has a staggering problem. I have made an amazing finding. This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter. Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus. “The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine. There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine. This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. “So, it means that the DNA can easily enter the genome. This is such an alarming problem. It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.” https://expose-news.com/2024/03/17/sv40-a-dna-altering-carcinogenic-contaminant-found-in-pfizers-covid-19-vaccines/
    EXPOSE-NEWS.COM
    SV40, a DNA Altering, Carcinogenic Contaminant, found in Pfizer’s COVID-19 Vaccines
    It’s not just the spike protein and the mRNA that are a problem. Both Pfizer and Moderna covid injections also have DNA contamination and Pfizer’s covid injection contains SV40 promoters. Mic…
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  • COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers.

    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    (CROCOTHERY/Shutterstock)
    Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA.

    The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed.
    These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times.
    DNA Integration

    Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome.

    Story continues below advertisement

    “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA.
    Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research.

    Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines.

    Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA.

    Story continues below advertisement

    After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk.

    However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear.

    Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory.

    Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said.

    Story continues below advertisement

    “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times.

    Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results.

    The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients.

    Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells.

    Story continues below advertisement

    However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data.
    His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12.

    “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said.
    Not Random Events

    The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12.

    Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random.

    Story continues below advertisement

    “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA.

    Highly activated DNA tends to play important roles in the human body.

    The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change.
    Vaccine DNA Is Active in the Cells

    Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times.

    Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA.

    Story continues below advertisement

    These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells.

    Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors.

    What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said.
    DNA Contamination From mRNA Vaccine Manufacturing

    DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process.
    This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency.
    The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance.
    Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA.

    However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine.

    In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination.

    However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this.
    Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose.
    Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells.

    https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184
    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers. COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher (CROCOTHERY/Shutterstock) Following his discovery of DNA contamination in COVID-19 mRNA vaccines, genomic researcher Kevin McKernan has recently found that the DNA in these vaccines can potentially integrate into human DNA. The COVID-19 vaccine spike sequence was detected in two types of chromosomes in cancer cell lines following exposure to the COVID-19 mRNA vaccine. Mr. McKernan’s findings, which he presents on his Substack blog, haven’t been peer-reviewed. These are expected to be “rare events,” but they can happen, Mr. McKernan told The Epoch Times. DNA Integration Since the introduction of the COVID-19 mRNA vaccines, some members of the public have been concerned that the vaccines may modify human DNA by combining their sequences with the human genome. Story continues below advertisement “Fact-checkers” refuted this, saying mRNA cannot be changed into DNA. Yet Mr. McKernan’s earlier work shows that DNA in the vaccine vials may be capable of changing human DNA. Ulrike Kämmerer, a professor of human biology at the University Hospital of Würzburg in Germany, conducted earlier stages of this research. Exposing breast and ovarian human cancer cells to Pfizer and Moderna mRNA vaccines, Ms. Kämmerer found that about half of the cells expressed the COVID-19 spike protein on their cellular surface, indicating that they had absorbed the vaccines. Mr. McKernan then performed gene sequencing and found that these cells and their descendant cells contained vaccine DNA. Story continues below advertisement After this, he tested to see whether any vaccine DNA combined with the cancer cell DNA, a process known as DNA integration. Integration is more of a concern in healthy cells than cancer cells because it disrupts cells’ genetic stability and integrity, increasing cancer risk. However, because cancer cells already have unstable DNA, the effects of DNA integration are less clear. Currently, in biomedical research, most experiments are carried out in cancer cell lines, as they are easier to obtain, experiment on, and maintain in the laboratory. Mr. McKernan detected vaccine DNA sequences on two chromosomes in the cancer cell lines: chromosome 9 and chromosome 12. The sequencing machine detected both instances of integration twice. It is important to get two readings of the DNA integration to ensure that the integration is not a result of misreading or random error, he said. Story continues below advertisement “The integration of ‘vaccine’ genetic information into the genome of cells was not such a surprise for me—more the confirmation of what we had to expect, unfortunately,” he told The Epoch Times. Mr. McKernan said it is unsurprising that integration was detected on only two chromosomes with two readings of each integration. This is because integration is rare, and the genes must be sequenced many times to get more sensitive results. The current findings are still preliminary, he said. More tests are also needed to determine whether DNA integration could be passed on to descendant cancer cells and whether this may affect cancer patients. Also, since the test was conducted in cancer cells and not in healthy human cells, it does not suggest the same integration would occur in healthy human cells. Story continues below advertisement However, Hiroshi Arakawa, a researcher at the Institute of Molecular Oncology who has a doctorate in molecular biology and immunology, wrote in his blog that “what happens in cultured cells can also occur in normal cells” after examining Mr. McKernan’s data. His review of Mr. McKernan’s data also found signs of DNA integration at chromosomes 9 and 12. “A wide variety of abnormalities can occur [in normal cells] depending on the site of genome integration,” Mr. Arakawa said. Not Random Events The two integration events into chromosome 9 occurred at the same place, as did the integration events into chromosome 12. Mr. McKernan said the odds of this occurring are one in 3 billion, highlighting that where the DNA integrates may not be random. Story continues below advertisement “There’s likely hotspots for this,” he told The Epoch Times, highlighting that in the human genome, jumping genes—short segments of DNA sequences—tend to “jump” into highly activated areas of DNA. Highly activated DNA tends to play important roles in the human body. The DNA integration into chromosome 12 occurred within the FAIM2 gene. Once activated, this gene creates a protein involved in programmed cell death. Since cancer cells evade cell death, the integration at chromosome 12 may be a survival-driven change. Vaccine DNA Is Active in the Cells Mr. McKernan said he believes that vaccine DNA is highly active in cancer cells. His sequencing machine detected the DNA of cancer cells 30 times but detected spike DNA 3,000 times. Not only did he detect much higher levels of vaccine DNA, but he also detected new variants in certain segments of the vaccine DNA. Story continues below advertisement These new DNA variations were not observed in unvaccinated cancer cells nor in the vaccine not exposed to the cancer cells. Mr. McKernan said he believes that these new gene variants likely occurred because the cancer cell made copies of the vaccine DNA and created small errors. What he and his team have found contradicts the latest arguments from fact-checkers claiming that the DNA from the mRNA vaccines cannot get into the cell, nor can it be active, he said. DNA Contamination From mRNA Vaccine Manufacturing DNA is present in the COVID-19 mRNA vaccines because of the manufacturing process. This has been verified by the U.S. Food and Drug Administration (FDA), Health Canada, and the European Medicines Agency. The mRNA vaccines are made from DNA; some of this DNA persists in the final product because of insufficient clearance. Initially, Pfizer reported that it would use a PCR machine to produce the DNA for its mRNA vaccine. The PCR machine first makes many copies of DNA, which is then sequenced into RNA. However, because this process wouldn’t be fast enough to meet demands, the vaccine manufacturers switched to using bacteria to mass-produce DNA as the template for the mRNA vaccine. In this process, vaccine manufacturers introduce bacterial DNA containing the vaccine spike sequences. The bacteria make many copies of this spike DNA as they divide. This spike DNA is then harvested and transcribed into mRNA in a machine. The mRNA is then packaged into lipid nanoparticles for use in vaccination. However, some bacterial DNA containing spike protein and other sequences could be packaged into lipid nanoparticles during the process, which would then be transported into cells during vaccination. Mr. McKernan’s earlier works have demonstrated this. Works by molecular virologist David Speicher have shown that the amount of DNA in the mRNA vaccine vials is higher than the FDA’s allowable threshold of 10 nanograms per vaccine dose. Mr. McKernan highlighted that compared with previous vaccines, mainly composed of naked DNA that had difficulty entering the cells, the DNA carried in the mRNA vaccines presents greater health risks, as it is packed into lipid nanoparticles and delivered straight into the cells. https://www.theepochtimes.com/health/covid-vaccine-gene-could-integrate-into-human-cancer-cells-researcher-5604184
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    COVID Vaccine Gene Could Integrate Into Human Cancer Cells: Researcher
    What Mr. McKernan and his team have found contradicts the latest arguments from fact-checkers.
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  • DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA

    Rebekah Barnett
    Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can.

    The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells.

    Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say.

    And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say.

    However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA.

    TLDR

    1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable)

    2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient)

    3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination

    4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA.
    Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process.

    McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.”

    Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients.

    But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan.

    While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration.

    Now, the first results are in.

    In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine.

    The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites.

    “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says.

    “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.”

    To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls.

    The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan.

    Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA.

    This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with.


    Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack
    Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA.

    “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.”

    Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan.


    Source: Kevin McKernan’s Substack
    Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line.

    You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’

    ‘Major advance,’ but clinical implications are limited

    McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.”

    “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries.

    The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells.

    McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately.

    At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan.

    The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety.

    Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English).

    LNPs deliver contaminant DNA straight to the cells

    A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur.

    This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes.

    This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems.


    Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021
    From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.”

    It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis.

    Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines.

    Regulators unconcerned

    I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment.

    The TGA did not address the new findings, but a spokesperson from the TGA responded,

    “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.”

    However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims.

    Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised.

    Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted.

    In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year.

    Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories.

    Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning.

    Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further.

    The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk.

    ‘No excuse’ for ignoring ‘screaming hot signal’

    Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan.

    Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.”

    “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?”

    There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years.

    “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.”


    Source: National Human Genome Research Institute
    DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination.

    “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.”

    Scientists pick up regulators’ slack

    In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton.

    “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.”

    Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites.

    In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in.

    “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said.

    McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present.

    Decentralisation the future of science?

    McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust.

    “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan.

    “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“

    In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world.


    Source: X
    For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation.

    “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan.

    Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet.

    Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct.


    Source: X
    In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.”

    But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa.

    Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not.

    The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received.

    View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files.

    Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina.

    Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account.


    To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks!

    Follow me on X

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    1
    From an article I wrote for Umbrella News on this topic last year:

    The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News,

    “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.”

    “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.”

    With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected).

    As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims.

    The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken.

    Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed.


    https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows It also appears that the contamination enters the cell nucleus and integrates with human DNA Rebekah Barnett Regulators and fact checkers claim that plasmid DNA contamination in the mRNA Covid vaccines can’t change your genomic DNA, but new evidence suggests that it actually can. The fact checkers assert that DNA contamination poses no risk to your genomic DNA because your body will naturally destroy any contaminant DNA before it even gets into the cells. Even if the contaminant DNA could get into cells, there’s no way it can enter the cell nucleus, where genomic integration events occur, they say. And even if the contaminant DNA could enter the nucleus, which it can’t, it still couldn’t genomically integrate unless specific enzymes are present, they say. However, results from independent lab testing conducted on ovarian cancer cell lines show that contaminant DNA from Pfizer’s Covid vaccine not only crossed into the cells, but that it survived multiple cell divisions. This is suggestive that the contaminant DNA is able to transfect (enter) the cell nucleus, and that it integrated with the human cell DNA. TLDR 1. Scientists claim that Pfizer vaccine contaminant DNA has been detected in ovarian cancer cell line DNA, but they do not yet know if it’s chromosomal (heritable) or extra-chromosomal DNA (not heritable) 2. This is an in vitro (in a lab dish) finding, and needs to be replicated in vivo (in a human patient) 3. As the finding is specific to cancer cell lines, it is not generalisable, but scientists say it may give an indication of what cancer patients in remission could experience after mRNA Covid vaccination 4. This finding calls into question fact checker claims that mRNA Covid vaccine DNA contamination can't enter cells, can't enter the nucleus, and cannot integrate with human DNA. Last year, Boston-based genomics scientist Kevin McKernan made the shocking discovery that the mRNA Covid vaccines are contaminated with excessive levels of plasmid DNA, an artefact of the vaccine production process. McKernan’s findings were soon confirmed by multiple independent labs around the world for both the Pfizer and Moderna mono- and bi-valent vaccines, including lots approved for children, with one Canadian study led by Dr David Speicher concluding that there are “billions to hundreds of billions of DNA molecules per dose.” Scientists including McKernan, University of South Carolina cancer genomics scientist Dr Phillip Buckhaults, and Dr Wafik El-Diery, head of the Cancer Centre at Brown University, expressed concerns that fragments of plasmid DNA contamination could cause adverse events, autoimmune problems and cancers in some patients. But perhaps most significantly, there is also a theoretical risk of the contaminant DNA integrating with patients’ chromosomal DNA and modifying the human genome. This is of particular concern with the Pfizer vaccine, which contains an SV40 enhancer sequence, used in gene therapies “to drive DNA into the nucleus,” explains McKernan. While regulators have taken a ‘wait and see’ approach, independent scientists, including McKernan, have been more proactive, initiating experiments testing for evidence of genomic integration. Now, the first results are in. In an experiment conducted together with German molecular biologist Dr Ulrike Kämmerer, McKernan has detected vaccine contaminant DNA in ovarian cancer cell lines treated with Pfizer’s Covid vaccine. The scientists found a chimeric combination of human ovarian cell line DNA and spike sequence DNA derived from the contaminating plasmid at at least one, and possibly two sites. “If anything, this work has put to bed the question regarding if this contaminant DNA gets into the cell, and the chimeric human and contaminant spike DNA sequences imply it has entered the nucleus,” McKernan says. “The PCR and sequencing data both demonstrate the vaccine is getting into the cell and surviving cell passaging. It is likely bioactive and being partially replicated.” To reach this finding, Dr Kämmerer first treated ovarian cancer cell lines with mRNA Covid vaccines, using cells treated with AstraZeneca and Janssen vaccines as controls. The cells were then ‘passaged’, meaning they were left to divide and replicate numerous times. This has the effect of “rinsing away residual vaccine,” explains McKernan. Immunohistochemistry (IHC) was then performed, a staining process that Dr Kämmerer used to detect levels of spike protein expression produced by the vaccine modified-RNA. This was to confirm that the lipid nanoparticles (LNPs) carrying mod-RNA and plasmid DNA contamination “did their job and delivered the payload,” says McKernan. Measuring how many cells expressed spike protein also allowed the scientists to determine how much of the vaccine to treat the cells with. Immunohistochemistry performed with Pfizer top left, AstraZeneca top right as a control. Source: Kevin McKernan’s Substack Cell lines were then sent in cold storage to McKernan’s Boston lab, where his team used qPCR to screen which samples to sequence the cell line DNA. “What we found is, [contaminant] DNA that is getting transfected into ovarian cancer cell lines is replicating in the cells,” says McKernan, noting that the ratio of vaccine contaminant DNA to human cell DNA was “higher than we expected.” Chimeric sequences of human and vaccine contaminant DNA were detected at two sites: chromosomes 9 and 12, with the evidence for the latter being the strongest. “But we don't know if it's extra-chromosomal or whether it's chromosomal because of the Illumina (short read) method we used to sequence,” explains McKernan. Source: Kevin McKernan’s Substack Extra-chromosomal DNA is not part of the chromosome, and is therefore less likely to replicate and to be heritable. Chromosomal DNA, on the other hand, is heritable and more likely to be replicated. A third category, mitochondrial DNA, is heritable, but only from the maternal line. You can read a detailed account of methods and findings via McKernan’s Substack article, ‘Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2.’ ‘Major advance,’ but clinical implications are limited McKernan emphasises that these findings cannot be generalised, stating that “it is too early to make comments on the clinical implications.” “The study is performed in ovarian cancer cell lines. It is not performed in patient cells, but this is a proxy for what might happen in an ovarian cancer patient who's in remission,” says McKernan, especially as there is evidence that the LNPs go to the ovaries. The risk for patients in this scenario is that integration events with contaminant DNA might cause aberrant cell growth, which poses a risk to immune suppression of new cancer cells. McKernan notes that his experiment only picked up on putative integration events that persisted after multiple cell replications. That is to say, the scientists were not able to detect integration events that may have occurred, but then died off immediately. At the moment, no one knows how many integration events might be occurring, or what effect that would have on patients. “The unknowns are just exponential,” says McKernan. The cancer cell line experiment can be said to be “a microcosm of genome integration of contaminated DNA,” said Japanese molecular oncology scientist Hiroshi Arakawa, in his own analysis of McKernan and Dr Kämmerer’s experiment, published to his popular science blog on which he shares critical views on Covid vaccine safety. Akira calls the two possible integrations observed in Dr Kämmerer’s experiment a “major advance” laying the ground for further experimentation. “What happens in cultured cells can also occur in normal cells, and a wide variety of abnormalities can occur depending on the site of genome integration,” such as “the induction of cancer or malignant transformation,” he wrote (translated from Japanese to English). LNPs deliver contaminant DNA straight to the cells A key assumption underlying claims that mRNA Covid vaccine contamination cannot enter the cell nucleus, and cannot genomically integrate with host DNA, is that the contamination will never make it into dividing cells, which would be required for integration to occur. This is based on the assumption that the LNPs containing both mod-RNA and contaminant DNA mostly stay in the muscle at the injection site. As muscle cells do not divide, there’s no problem, the logic goes. This is misleading, however, as Pfizer’s own biodistribution data shows that the LNPs enter the blood and every major organ system, including the ovaries, as mentioned above. While it is true that muscle cells don’t divide, LNPs distributed around the body can transfect any number of dividing cells in various organ systems. Table 4-2. shows biodistribution of LNPs, Pfizer Nonclinical Evaluation Report, 2021 From there, it’s only a matter of time before the LNP contents get into the cell nucleus, says McKernan. “In any dividing cell, the nucleus dissolves. So, when people say the DNA can get into the cytoplasm [inside the cell membrane] but won't get into the nucleus, well, in any dividing cell, it will end up getting into the nucleus.” It is possible that the dissolution of the cell nucleus during division is the mechanism underlying McKernan and Dr Kämmerer’s observed passaging of contaminant DNA, but further research will be required to confirm or disprove this hypothesis. Because of the effectiveness of LNPs in delivering their contents into cells, McKernan, Dr Buckhaults and Dr Speicher have questioned the suitability of the current regulatory limits on contaminant DNA in vaccines, which were set prior to the introduction of LNP technology in vaccines. Regulators unconcerned I sent McKernan’s Substack article documenting the new DNA integration findings to Australia’s drug regulator, the Therapeutic Goods Administration, for comment. The TGA did not address the new findings, but a spokesperson from the TGA responded, “The Department of Health and Aged Care has every confidence in the safety, quality and efficacy of the various approved COVID-19 vaccines for use in Australia. The TGA’s assessment of all vaccines is based upon high quality evidence, including studies and reviews published in peer-reviewed scientific and clinical journals.” However, when asked previously to provide evidence for its position that Covid vaccines pose no risk of DNA integration, the TGA provided no peer-reviewed scientific evidence to support its claims. Instead, the TGA provided links to a Mayo Clinic fact page with no scientific citations, an article by the discredited RMIT FactLab, and a scientific commentary article suggesting that in vitro findings cannot be generalised. Furthermore, TGA has not been forthcoming with the evidence it does hold. When asked to release Covid vaccine batch testing results under Freedom of Information, the regulator provided all 74 pages - fully redacted. In the US, the Food and Drug Administration (FDA) denied that contaminant DNA in the mRNA vaccines can enter the nucleus or pose any threat to patients’ genomic DNA, in a response to concerns raised by Florida Surgeon General, Dr Joseph A. Ladapo in December of last year. Additionally, the FDA misleadingly refuted the presence of SV40 proteins in the vaccines, when in fact Dr Ladapo raised concerns over the presence of an SV40 enchancer sequence in the Pfizer vaccine, as confirmed by Health Canada and numerous independent laboratories. Such ham-fisted mischaracterisation of a gene therapy sequence by the FDA is suggestive of either gross incompetence, or a disinformation play. Both are concerning. Science journalist Maryanne Demasi reported, in November last year, that the FDA shut down her enquiries into the DNA contamination matter, refusing to confirm if it found levels of DNA that exceeded acceptable levels, or if it was investigating further. The presence of contamination has been officially acknowledged by the European Medicines Agency (EMA) and Health Canada, with the latter also acknowledging the presence of the SV40 enhancer sequence, though both regulators deny that the amounts exceed regulatory limits, or that the DNA contamination poses any risk. ‘No excuse’ for ignoring ‘screaming hot signal’ Instead of denying excessive DNA levels and deferring to manufacturers’ reported test results, regulators should run their own qPCR testing on batch lots, says McKernan. Then, “they would see what everyone else is seeing, which is that sometimes the CT scores come out as low as 13… that’s a screaming hot signal.” “As a reference, the Covid test would call people positive at 33-35,” McKernan explains. “That’s a million-fold difference (20 CTs). A million-fold less Covid RNA and you're positive and quarantined. But you can inject a million-fold more past your mucosa?” There’s “no excuse” for regulators to not sequence every vaccine lot, says McKernan, when the costs for doing so have dropped dramatically in recent years. “DNA sequencing costs have dropped 100,000 fold in the last decade. They have relaxed the DNA contamination limits 1000-fold in this time frame. It likely only costs $1,000 in reagents for millions-to-billions of dollars worth of product.” Source: National Human Genome Research Institute DNA sequencing by regulatory agencies is important not just for measuring quantities, says McKernan, but also for determining the type of DNA contamination. “Not all DNA is created equal. Some is designed to replicate - when it gets into a cell, it can make more of itself. It's a massive loophole in the regulations that they don't do sequencing. But it's never been cheaper. You can precisely know the nature of the DNA in every single vial.” Scientists pick up regulators’ slack In the absence of any regulatory appetite for investigating the risks of DNA contamination in the mRNA Covid shots, and particularly the risk of genomic integration, independent scientists have taken the baton. “We are writing up our findings and will publish a preprint soon,” says McKernan, who is planning further testing in partnership with Dr Kämmerer. “We’re doing more experiments first. We need to sequence deeper to find out if the integration events are in chromosomal or extra-chromosomal DNA.” Dr Buckhaults is also running his own experiment, calling for de-identified samples of tumours or fresh blood from pathology and hematology labs. These samples will be tested for the presence of plasmid DNA contamination, with whole genome sequencing to then be carried out on positive samples to identify genomic integration sites. In an email outlining his experiment, Dr Buckhaults told me that he intends to report his findings in a peer-reviewed publication, predicting that the work could take “a few months to a year,” depending on how fast samples come in. “I am hopeful to prove my concerns are unwarranted by accumulating a lot of negative data, and of course negative data takes the most time to collect,” he said. McKernan says he is aware of other labs running tests for contaminant plasmid DNA integration, but cannot disclose the details at present. Decentralisation the future of science? McKernan says he has experienced some pushback for publishing his methods and findings in real time via Substack, X, and preprints. But, he believes that making his data available as quickly as possible is a way for the field of science to regain public trust. “Many will criticize our disclosure of preliminary findings but we feel this is an insult to the intelligence of the average person,” says McKernan. “It's a form of scientific elitism that implies people can't handle the truth and will be scared like sheep if given a glimpse of how the true scientific process is performed. Scientists are 90% of the time wrong but only publish the times when they are right. There is no journal of negative results.“ In light of the prospect that most published research findings are false (as famously asserted in a 2005 article by Professor John Ioannidis), McKernan questions the value of peer-review, instead favouring replication or refutation in the real world. Source: X For this reason, McKernan says he has not prioritised peer-reviewed publication for his DNA contamination findings, but is rather focusing on conducting more experiments and releasing the data as he goes - even when it’s incomplete, or requires further experimentation. “We were not expecting to find any integration events at this depth of coverage, but they are evident to anyone who downloads our public reads. To not speak to obvious evidence in such data would be irresponsible even when such evidence doesn't 100% answer a given question,” says McKernan. Dr Buckhaults takes a somewhat different view. After sharing his initial plasmid DNA contamination findings in a South Carolina Senate hearing in September last year, the video recording broke the internet. Believing the hearing to have been private, Dr Buckhaults was alarmed that the widespread distribution of his testimony may have caused “unintended, harmful side effects.” He requested that YouTube take down his testimony video, which is now defunct. Source: X In our correspondence, Dr Buckhaults stressed that while more research is warranted, he is of the opinion that the public “should not overreact to the news of the plasmid DNA contamination. It's serious enough that scientists need to hustle and figure out if it's causing any health problems now or down the road, but it's not cause for the general public to be alarmed.” But, “The reality is that`transfection experiments with contaminated DNA' have been carried out on vast numbers of people around the world in the name of vaccination,” writes Arakawa. Perhaps the experiment participants will be the ones to decide if they should be alarmed, or not. The FDA was contacted for comment about Dr Kämmerer and McKernan’s new findings, but they did not respond by publication deadline. This article will be updated if comment is received. View Kevin McKernan’s write up of his DNA integration experiment (in partnership with Dr Kämmerer) here. Scroll down for links to sequencing data files. Pathology and hematology labs wishing to send samples to Dr Buckhaults are invited to contact him at the University of South Carolina. Update 23 March 2024: This article was edited to add mention of the Dr David Speicher et al. finding of “billions to hundreds of billions of DNA molecules per dose” of the mRNA vaccines, and the scientists’ concerns that regulatory limits on DNA contamination have not taken LNP transfection into account. To support my work, make a one-off contribution to DDU via my Kofi account and/or subscribe. Thanks! Follow me on X Follow me on Instagram 1 From an article I wrote for Umbrella News on this topic last year: The TGA maintains that allegations put forward in the case about the potential for mRNA vaccines to alter the recipient’s DNA are unfounded. A spokesperson for the TGA told Umbrella News, “COVID-19 vaccines do not alter a person’s DNA. The mRNA in the vaccines does not enter the nucleus of cells and is not integrated into the human genome. Thus, the mRNA does not cause genetic damage or affect the offspring of vaccinated individuals.” “The TGA continues to monitor the scientific literature associated with the SARS – CoV-2 virus and the various COVID-19 vaccines approved for use in Australia.” With reference to the specific studies cited in the case materials, the TGA pointed Umbrella News to an RMIT ABC Fact Check post from 2022 purporting to ‘debunk’ claims that mRNA jabs are genotoxic. This is the same site that ‘debunked’ claims that COVID vaccines can cause menstrual disruption, before peer-reviewed scientific studies proved that they can and do (the post has not been corrected). As evidence that it is “well established” that vaccine mRNA and protein do not enter the nucleus, the TGA provided a link to a Mayo Clinic fact page which provides no studies or scientific evidence in support of its claims. The TGA did provide one commentary article published in a scientific journal which pointed out that the in vitro liver cell line study cannot be extrapolated to generalise about in vivo findings (in a human, not a dish) without further research being undertaken. Additionally, RMIT FactLab was suspended by Facebook in August 2023 after an uproar over its blatantly biased and factually dubious ‘fact checking’ of media articles relating to the Voice referendum campaign. It also transpired that RMIT FactLab had falsely represented its accreditation with the International Fact-Checking Network as current, when it had in fact lapsed. https://news.rebekahbarnett.com.au/p/dna-contamination-in-covid-vaccines
    NEWS.REBEKAHBARNETT.COM.AU
    DNA contamination in Covid vaccines DOES get into human cells, new evidence shows
    It also appears that the contamination enters the cell nucleus and integrates with human DNA
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  • Medical Researchers Call for Urgent Actions to Deal with Mass Contamination of Blood Supply
    "Japanese researchers have published disturbing evidence that blood transfusions from individuals who received COVID-19 shots are tainted with a myriad of dangers." - Jeff Dornik

    Karen Kingston
    March 22, 2024: Japanese researchers published a meta-analysis on the dangers of using blood donated from people who were injected with the COVID-19 ‘vaccines,’ increasing the risks for acute health conditions and severe diseases in recipients of blood donations. The researchers provide testing and screening recommendations, and proposed regulations to reduce these risks.


    Share

    Jeff Dornik published an excellent article summarizing the scientific meta-analysis, declaring;

    “The blood supply, once deemed a lifeline, has now become a conduit for harm.” - Jeff Dornik


    In his article entitled, Japanese Researchers Sound Alarm on Deadly Risks of Vaccinated Blood Transfusions, Jeff writes, “In a shocking revelation, Japanese researchers have unearthed disturbing evidence that could change the way we view COVID-19 Injections forever. According to their findings, blood transfusions from individuals who have received COVID-19 shots are tainted with a myriad of dangers, potentially wreaking havoc on both vaxxed and unvaxxed recipients. This discovery has sparked urgent calls for action from the global medical community, as the ramifications of this contamination could be catastrophic.”

    I recommend reading and sharing Jeff’s breaking news article.

    You Can Make an Impact

    The COVID-19 injections have not only contaminated the blood of those who are injected, but due to shedding and blood donations, all individuals are at risk of being inoculated with gene-editing nanoparticle technologies and toxic biosynthetic spike proteins. These toxic biosynthetic nanoparticles are proven to increase the risk for cardiovascular, neurological, auto-immune, and pulmonary diseases, and can induce permanent changes to the human genome.


    For the safety of the public, the use of mRNA nanoparticle injections must be banned from every county and state in America.

    Every American has standing in their state to demand that the COVID-19 mRNA nanoparticle ‘vaccines’ be banned from their state. You can send a demand letter to your governor, attorney general, and even local sheriff. If they fail to take action, you can petition your state’s Supreme Court to order the governor and attorney general to seize the injections and ban the use of mRNA nanoparticle injections.

    Hebrews 10:35-36

    So do not throw away your confidence; it will be richly rewarded. You need to persevere so that when you have done the will of God, you will receive what he has promised.

    Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida?

    Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida?
    March 5, 2024: When I first began this endeavor, God put on my heart to have the mRNA shots removed from every community across the United States and around the world. I’m honored that I was integral in sending Dr. Joseph Sansone the document that I updated from the

    Read full story

    The Kingston Report. TRUTH WINS.

    Ways to Support My Work

    Mail: Karen Kingston/miFight Inc., 960 Postal Way #307, Vista, CA 92085

    Buy me a coffee (Ko-fi)

    Consider becoming a free or paid subscriber.

    email: [email protected]

    Get a FREE $99 Wellness Company Membership

    You can keep a full armamentarium of prescriptions on-hand for bacterial, viral, or parasite infections through The Wellness Company. Use the code FREEMEMBER at checkout and SAVE $45.


    Here is the direct link to Emergency Prescription Kit, which contains prescriptions for the above listed acute (not chronic) conditions and infections. Use the code FREEMEMBER at checkout and SAVE $45 PLUS Receive a FREE TWC Membership ($99 Value)


    https://karenkingston.substack.com/p/medical-researchers-call-for-urgent
    Medical Researchers Call for Urgent Actions to Deal with Mass Contamination of Blood Supply "Japanese researchers have published disturbing evidence that blood transfusions from individuals who received COVID-19 shots are tainted with a myriad of dangers." - Jeff Dornik Karen Kingston March 22, 2024: Japanese researchers published a meta-analysis on the dangers of using blood donated from people who were injected with the COVID-19 ‘vaccines,’ increasing the risks for acute health conditions and severe diseases in recipients of blood donations. The researchers provide testing and screening recommendations, and proposed regulations to reduce these risks. Share Jeff Dornik published an excellent article summarizing the scientific meta-analysis, declaring; “The blood supply, once deemed a lifeline, has now become a conduit for harm.” - Jeff Dornik In his article entitled, Japanese Researchers Sound Alarm on Deadly Risks of Vaccinated Blood Transfusions, Jeff writes, “In a shocking revelation, Japanese researchers have unearthed disturbing evidence that could change the way we view COVID-19 Injections forever. According to their findings, blood transfusions from individuals who have received COVID-19 shots are tainted with a myriad of dangers, potentially wreaking havoc on both vaxxed and unvaxxed recipients. This discovery has sparked urgent calls for action from the global medical community, as the ramifications of this contamination could be catastrophic.” I recommend reading and sharing Jeff’s breaking news article. You Can Make an Impact The COVID-19 injections have not only contaminated the blood of those who are injected, but due to shedding and blood donations, all individuals are at risk of being inoculated with gene-editing nanoparticle technologies and toxic biosynthetic spike proteins. These toxic biosynthetic nanoparticles are proven to increase the risk for cardiovascular, neurological, auto-immune, and pulmonary diseases, and can induce permanent changes to the human genome. For the safety of the public, the use of mRNA nanoparticle injections must be banned from every county and state in America. Every American has standing in their state to demand that the COVID-19 mRNA nanoparticle ‘vaccines’ be banned from their state. You can send a demand letter to your governor, attorney general, and even local sheriff. If they fail to take action, you can petition your state’s Supreme Court to order the governor and attorney general to seize the injections and ban the use of mRNA nanoparticle injections. Hebrews 10:35-36 So do not throw away your confidence; it will be richly rewarded. You need to persevere so that when you have done the will of God, you will receive what he has promised. Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida? Pending Florida Supreme Court Case: Will DeSantis & AG Moody Be Court-Ordered to Remove ALL mRNA Injections from Florida? March 5, 2024: When I first began this endeavor, God put on my heart to have the mRNA shots removed from every community across the United States and around the world. I’m honored that I was integral in sending Dr. Joseph Sansone the document that I updated from the Read full story The Kingston Report. TRUTH WINS. Ways to Support My Work Mail: Karen Kingston/miFight Inc., 960 Postal Way #307, Vista, CA 92085 Buy me a coffee (Ko-fi) Consider becoming a free or paid subscriber. email: [email protected] Get a FREE $99 Wellness Company Membership You can keep a full armamentarium of prescriptions on-hand for bacterial, viral, or parasite infections through The Wellness Company. Use the code FREEMEMBER at checkout and SAVE $45. Here is the direct link to Emergency Prescription Kit, which contains prescriptions for the above listed acute (not chronic) conditions and infections. Use the code FREEMEMBER at checkout and SAVE $45 PLUS Receive a FREE TWC Membership ($99 Value) https://karenkingston.substack.com/p/medical-researchers-call-for-urgent
    KARENKINGSTON.SUBSTACK.COM
    Medical Researchers Call for Urgent Actions to Deal with Mass Contamination of Blood Supply
    "Japanese researchers have published disturbing evidence that blood transfusions from individuals who received COVID-19 shots are tainted with a myriad of dangers." - Jeff Dornik
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  • Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid
    Rhoda WilsonMarch 20, 2024
    There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies’, what other genetic experimentations continue unhindered out there?” he asks.

    In May 2020, Dr. Maavak wrote an article about how SARS-CoV-2 was not germinated in a vacuum. The Wuhan Institute of Virology conducted research with alarming global parallels including the pursuit of superintelligence and the development of chimaeras, or interspecies hybrids.

    What he wrote in May 2020 is still relevant today, he says. So yesterday, Dr. Maavak reposted his now four-year-old article.

    Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…

    Coronavirus in a Time of Chimaeras and Beyond

    By Dr. Mathew Maavak

    In May 2020, just as the coronavirus made hourly headlines, I had suspected that the virus was part of a much more sinister agenda. What I wrote back then remains just as relevant today. Here it is.

    Genetically-Enhanced Competitiveness

    The Sars-Cov-2 virus, which allegedly causes covid-19, was not germinated in a vacuum. The type of research conducted at the Wuhan Institute of Virology had ominous analogues worldwide. These included the quest for super intelligence and the development of interspecies hybrids or chimaeras.

    What began as a scientific mission to remedy congenital defects has rapidly morphed into a global race to create designer babies, super soldiers and transhumans through the aid of biotechnology, artificial intelligence and/or machine-neuralinking. 21st century eugenics is tacitly justified by the need to boost “national competitiveness.”

    China leads the way here. In one revealing episode, genome sequencing giant BGI Shenzhen had procured and sequenced the DNA of more than 2,000 people – mostly Americans – with IQ scores of at least 160. According to Stephen Hsu, a theoretical physicist from Michigan State University and scientific adviser to BGI:

    An exceptional person gets you an order of magnitude more statistical power than if you took random people from the population …

    BGI Shenzhen intends to become a “bio-Google” that will collate the “world’s biological information and make it universally accessible and useful.” From 2012 onwards, it began collaborating with the Bill & Melinda Gates Foundation (“BMGF”). No surprises there.

    Scientific endeavours like these are based on the assumption that an assemblage of smart samples can help in the identification and transplantation of optimal bits of genetic material into future generations.

    Can a virus or vaccine perform this transplantation? Or will such agencies be used to cull the majority of the human population before a “genetic antidote” emerges to reverse their lethal effects? It will be too late for the vast majority of mankind by then. artificial selection, backed by artificial intelligence, may decide who gets this new booster. But is such a hypothetical scenario even realistic? There are too many imponderables here but viruses, nasal swabs and “vaccines” will surely deliver vital data for the “New Human Genome Project.”

    New Eugenics Zeitgeist

    The science of eugenics is not dissuaded by the nurture over nature debate, even after exhaustive studies had failed to establish genetic variants associated with intelligence. For example, a 2010 study led by Robert Plomin, a behavioural geneticist at King’s College London, had probed over 350,000 variations in single DNA letters across the genomes of 7,900 children but found no prized variant. Curiously, most of the smart samples procured by BGI Shenzhen were sourced from Plomin’s research activities.

    Periodic setbacks did not deter the proponents of “procreative beneficence” who argue that it is a human duty to augment the genetic codes of future generations. Failure to do so is couched in terms of “genetic neglect” and even child abuse. If this sounds eerily familiar, look no further than the worldview which once animated the Western world before the Nazis elevated it to a whole new level altogether.

    The eugenics zeitgeist has gripped China in a big way. Under its Maternal and Infant Health Care Law (1994), foetuses with potential hereditary diseases or deformities are recommended for abortion. At the rate Beijing is building its eugenics utopia, the definition of deformity may ultimately include a genetically pre-diagnosed average IQ.

    Instead of inciting public outrage, the law precipitated a headlong rush to select “intelligent” babies through methods like preimplantation genetic diagnosis (“PGD”). The idea behind PGD is to screen and identify the most promising embryos for implantation and birth. Combined with CRISPR gene-editing tools, next-generation Chinese citizens are expected to exhibit remarkably higher IQs – at least according to bioethicists who fret over a future marked by the “genetic haves” and “genetic have-nots.” China already has three CRISPR-edited babies whose current fate remains unknown.

    In the aftermath of the corona psychosis, the availability of “smart samples” would have increased exponentially and may dovetail nicely with the eugenics agenda of the Rockefeller Foundation and BMGF. Incidentally, Bill Gates grew up in a household that was heavily invested in population control and eugenics.

    Our smart societies may inevitably face the existential question of “live-lets” and “live-nots” down the line. The orchestrated rebellion towards selective extinction, if it occurs, has a tragicomical public face: An autistic Swede who parrots the “listen to the science” and “listen to the experts” mantra.

    How will future designer babies contribute to society? For one thing, we will be missing individuals like Beethoven (deaf); Albert Einstein (learning disability/late development); John Nash (schizophrenia); Andrea Boccelli (congenital glaucoma) and Vincent van Gogh (chronic depression/anxiety) and a host of others like them. A future Stephen Hawking (motor neurone disease) and Greta Thunberg (Asperger’s Syndrome – allegedly) will be genetically disqualified before birth.

    It is now inconvenient to consider intelligence as a result of peer interactions, human environment and ingenious reactions to adversity. (I personally define intelligence as an ability to nip the bullsh*t in its foetid bud).

    Mapping out the complex and sometimes unpredictable interplay between 100 trillion synaptic connections in a human brain may take centuries to accomplish but that does not deter the utopians of today.

    After all, genetic manipulation is the eugenic wormhole that promises to accelerate the emergence of a super society at warp speed. The late billionaire paedophile, Jeffrey Epstein, was a prominent proponent of this philosophy. Epstein intended to breed a “super race of humans with his DNA by impregnating women at his New Mexico ranch, genetic engineering and artificial intelligence.” Welcome to Lebensborn 2.0!

    Prominent scientists linked to Epstein’s transhumanist fantasies included “molecular engineer George Church; Murray Gell-Mann, the discoverer of the quark; the evolutionary biologist Stephen Jay Gould; the neurologist and author Oliver Sacks; and the theoretical physicist Frank Wilczek.” The late Stephen Hawking – who will ironically flunk the genetic pre-screenings of tomorrow – was another Epstein associate.

    Forget about Mars missions; major powers see eugenics as the next great frontier. Its hyper-materialistic focus is encapsulated by the following analogy from Russian scientist Denis Rebrikov:

    It currently costs about a million roubles (US$15,500 at that time) to genetically change an embryo – more than a lot of cars – but prices will fall with greater use … I can see the billboard now: “You Choose: a Hyundai Solaris or a Super-Child?”

    You are comparing a child, super or not, with a Hyundai? I mean a Hyundai, really? Sometimes, the road to hell is paved with good intentions but most of the time, it begins with a diabolically silly proposition.

    But why stop at children? From genetically engineered horses in Argentina that are supposedly faster, stronger and better jumpers to super-dogs in China that are comprehensively superior to the average mutt, the DNA of the entire natural world is being slated for a revolutionary redesign.

    Crouching Chimaeras, Hideous Hybrids

    The masters of our universe however cannot create future generations of superhumans without being adept at recombining genetic sequences across species. That is the logic guiding eugenicists. As a result, a slew of chimaeras or interspecies hybrids have been spawned with the aid of CRISPR technology. These include ghastly human-monkey hybrids, monkey-pig hybrids, human-rabbit hybrids and a host of other lab-manufactured monstrosities.

    Chimaeras are created when human embryonic stem cells are injected into embryos of other species. The goal, for the time being, is to induce growth of targeted human organs. Those facing terminal illnesses will no longer have to worry about long organ waiting lists. Chinese scientists have just transplanted a modified pig liver into a brain-dead human and it seems to have worked.

    A less controversial approach to human organ replacement is 3D bioprinting or its 4D bioprinting iteration. These techniques involve the “printing” of a replacement organ from the stem cells of a transplant recipient, thereby eliminating the odds of organ rejection.

    But why stop at replacement organs when we can have “replacement humans” altogether? Future generations must think like Einsteins, be as nimble as leopards and possess owl-like night visions. And, of course, be virus-resistant as well!

    The manipulation of the human genome is the new “grand response” to the venerable set of “grand challenges” for 2030 and beyond. China is the go-to place for such genetic tinkering as some of these undertakings are technically illegal in the West. And this is where the utility of covid-19 comes into the picture. It provides the perfect pretext to remove such ethical constraints. After all, “Disease X” is just waiting to escape from the belly of some bat or pangolin …

    Since 2014, the Wuhan Institute of Virology has been the recipient of a two-stage grant worth $7.2 million from the United States government for gain-of-function research into bat coronaviruses. According to a Newsweek report in April 2020:

    Many scientists have criticised gain of function research, which involves manipulating viruses in the lab to explore their potential for infecting humans because it creates a risk of starting a pandemic from accidental release.

    Such caution has not deterred a flurry of research into microbial gene manipulation. The Wuhan experiments may have either spawned the Sars-Cov-2 virus or it may have provided a fraudulent context for future tyrannical mandates.

    But to solely blame China for the coronavirus “pandemic” is a tad unfair. Just as China is the factory of the world for foreign corporations, it is also the genetic incubator for a variety of viruses and chimaeras for foreign governments and foundations. Even so, the human-pig chimaera was the creation of the Salk Institute in California. Research into the world’s first human-mouse hybrid was largely a Japanese affair. The Portuguese in the meantime had created a virus chimaera.

    The United Kingdom, on their end, had spawned a human-cow hybrid embryo in 2008 – perhaps in keeping with the bovine disposition of those glued to the BBC. It was in Britain where the game-changing Dolly the Sheep was cloned in 1996.

    The transition from sheep to sheeple may turn out to be a short 21st century Jurassic Park ride.

    Coincidences and Consequences

    Before the advent of gene-editing tools and supercomputing, it would have been impossible to create a viable chimaera. The Biotech-Industrial Complex and contact tracing-type panopticons constitute a new growth area for Tech Titans that were once facing bankruptcy.

    The dangers of genome editing were in fact included in the Worldwide Threat Assessment reports submitted to the United States Congress in 2016 and 2017. These risks were either omitted or glossed over in the 2018 and 2019 reports – just as such risks gravitated to the high impact-high likelihood quadrant.

    Is it a coincidence that the nations most affected by covid-19 – at least during the first two years of its alleged spread – were the very ones that had either promoted or encouraged a variety of genetic experimentations that are contrary to nature? If – and that is a big “if” – these nations succeed in their quest for “designer babies” and “superhumans,” the rest of mankind will be rendered redundant. Some mass extermination event may transpire under the guise of World War III, food shortages, Disease X or a combination thereof.


    If everything goes according to plan, however, there will be 500 million potential specimens left for The Great Reset. The Third World, whose leaders are being monetarily incentivised to focus on unattainable Sustainable Development Goals (“SDGs”), will be consigned to the ash heaps of history.

    It is quite ironic that a new generation of cerebrally deficient “thought leaders” and “experts” are being groomed to promote the demises of their societies and themselves.

    About the Author

    Mathew Maavak, with a PhD in Policy Studies, specialises in systems science, global risks, strategic foresight, geopolitics and governance. He is a Malaysian expert on risk foresight and governance.

    Dr. Maavak has published numerous op-eds on a variety of eclectic subjects for over 20 years – by ‘connecting the dots’ in a disjointed world. He is the author of a Substack page titled ‘The Eye Opener’ which you can subscribe to and follow HERE.



    https://expose-news.com/2024/03/20/chimaeras-and-interspecies-hybrids/
    Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid Rhoda WilsonMarch 20, 2024 There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies’, what other genetic experimentations continue unhindered out there?” he asks. In May 2020, Dr. Maavak wrote an article about how SARS-CoV-2 was not germinated in a vacuum. The Wuhan Institute of Virology conducted research with alarming global parallels including the pursuit of superintelligence and the development of chimaeras, or interspecies hybrids. What he wrote in May 2020 is still relevant today, he says. So yesterday, Dr. Maavak reposted his now four-year-old article. Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox… Coronavirus in a Time of Chimaeras and Beyond By Dr. Mathew Maavak In May 2020, just as the coronavirus made hourly headlines, I had suspected that the virus was part of a much more sinister agenda. What I wrote back then remains just as relevant today. Here it is. Genetically-Enhanced Competitiveness The Sars-Cov-2 virus, which allegedly causes covid-19, was not germinated in a vacuum. The type of research conducted at the Wuhan Institute of Virology had ominous analogues worldwide. These included the quest for super intelligence and the development of interspecies hybrids or chimaeras. What began as a scientific mission to remedy congenital defects has rapidly morphed into a global race to create designer babies, super soldiers and transhumans through the aid of biotechnology, artificial intelligence and/or machine-neuralinking. 21st century eugenics is tacitly justified by the need to boost “national competitiveness.” China leads the way here. In one revealing episode, genome sequencing giant BGI Shenzhen had procured and sequenced the DNA of more than 2,000 people – mostly Americans – with IQ scores of at least 160. According to Stephen Hsu, a theoretical physicist from Michigan State University and scientific adviser to BGI: An exceptional person gets you an order of magnitude more statistical power than if you took random people from the population … BGI Shenzhen intends to become a “bio-Google” that will collate the “world’s biological information and make it universally accessible and useful.” From 2012 onwards, it began collaborating with the Bill & Melinda Gates Foundation (“BMGF”). No surprises there. Scientific endeavours like these are based on the assumption that an assemblage of smart samples can help in the identification and transplantation of optimal bits of genetic material into future generations. Can a virus or vaccine perform this transplantation? Or will such agencies be used to cull the majority of the human population before a “genetic antidote” emerges to reverse their lethal effects? It will be too late for the vast majority of mankind by then. artificial selection, backed by artificial intelligence, may decide who gets this new booster. But is such a hypothetical scenario even realistic? There are too many imponderables here but viruses, nasal swabs and “vaccines” will surely deliver vital data for the “New Human Genome Project.” New Eugenics Zeitgeist The science of eugenics is not dissuaded by the nurture over nature debate, even after exhaustive studies had failed to establish genetic variants associated with intelligence. For example, a 2010 study led by Robert Plomin, a behavioural geneticist at King’s College London, had probed over 350,000 variations in single DNA letters across the genomes of 7,900 children but found no prized variant. Curiously, most of the smart samples procured by BGI Shenzhen were sourced from Plomin’s research activities. Periodic setbacks did not deter the proponents of “procreative beneficence” who argue that it is a human duty to augment the genetic codes of future generations. Failure to do so is couched in terms of “genetic neglect” and even child abuse. If this sounds eerily familiar, look no further than the worldview which once animated the Western world before the Nazis elevated it to a whole new level altogether. The eugenics zeitgeist has gripped China in a big way. Under its Maternal and Infant Health Care Law (1994), foetuses with potential hereditary diseases or deformities are recommended for abortion. At the rate Beijing is building its eugenics utopia, the definition of deformity may ultimately include a genetically pre-diagnosed average IQ. Instead of inciting public outrage, the law precipitated a headlong rush to select “intelligent” babies through methods like preimplantation genetic diagnosis (“PGD”). The idea behind PGD is to screen and identify the most promising embryos for implantation and birth. Combined with CRISPR gene-editing tools, next-generation Chinese citizens are expected to exhibit remarkably higher IQs – at least according to bioethicists who fret over a future marked by the “genetic haves” and “genetic have-nots.” China already has three CRISPR-edited babies whose current fate remains unknown. In the aftermath of the corona psychosis, the availability of “smart samples” would have increased exponentially and may dovetail nicely with the eugenics agenda of the Rockefeller Foundation and BMGF. Incidentally, Bill Gates grew up in a household that was heavily invested in population control and eugenics. Our smart societies may inevitably face the existential question of “live-lets” and “live-nots” down the line. The orchestrated rebellion towards selective extinction, if it occurs, has a tragicomical public face: An autistic Swede who parrots the “listen to the science” and “listen to the experts” mantra. How will future designer babies contribute to society? For one thing, we will be missing individuals like Beethoven (deaf); Albert Einstein (learning disability/late development); John Nash (schizophrenia); Andrea Boccelli (congenital glaucoma) and Vincent van Gogh (chronic depression/anxiety) and a host of others like them. A future Stephen Hawking (motor neurone disease) and Greta Thunberg (Asperger’s Syndrome – allegedly) will be genetically disqualified before birth. It is now inconvenient to consider intelligence as a result of peer interactions, human environment and ingenious reactions to adversity. (I personally define intelligence as an ability to nip the bullsh*t in its foetid bud). Mapping out the complex and sometimes unpredictable interplay between 100 trillion synaptic connections in a human brain may take centuries to accomplish but that does not deter the utopians of today. After all, genetic manipulation is the eugenic wormhole that promises to accelerate the emergence of a super society at warp speed. The late billionaire paedophile, Jeffrey Epstein, was a prominent proponent of this philosophy. Epstein intended to breed a “super race of humans with his DNA by impregnating women at his New Mexico ranch, genetic engineering and artificial intelligence.” Welcome to Lebensborn 2.0! Prominent scientists linked to Epstein’s transhumanist fantasies included “molecular engineer George Church; Murray Gell-Mann, the discoverer of the quark; the evolutionary biologist Stephen Jay Gould; the neurologist and author Oliver Sacks; and the theoretical physicist Frank Wilczek.” The late Stephen Hawking – who will ironically flunk the genetic pre-screenings of tomorrow – was another Epstein associate. Forget about Mars missions; major powers see eugenics as the next great frontier. Its hyper-materialistic focus is encapsulated by the following analogy from Russian scientist Denis Rebrikov: It currently costs about a million roubles (US$15,500 at that time) to genetically change an embryo – more than a lot of cars – but prices will fall with greater use … I can see the billboard now: “You Choose: a Hyundai Solaris or a Super-Child?” You are comparing a child, super or not, with a Hyundai? I mean a Hyundai, really? Sometimes, the road to hell is paved with good intentions but most of the time, it begins with a diabolically silly proposition. But why stop at children? From genetically engineered horses in Argentina that are supposedly faster, stronger and better jumpers to super-dogs in China that are comprehensively superior to the average mutt, the DNA of the entire natural world is being slated for a revolutionary redesign. Crouching Chimaeras, Hideous Hybrids The masters of our universe however cannot create future generations of superhumans without being adept at recombining genetic sequences across species. That is the logic guiding eugenicists. As a result, a slew of chimaeras or interspecies hybrids have been spawned with the aid of CRISPR technology. These include ghastly human-monkey hybrids, monkey-pig hybrids, human-rabbit hybrids and a host of other lab-manufactured monstrosities. Chimaeras are created when human embryonic stem cells are injected into embryos of other species. The goal, for the time being, is to induce growth of targeted human organs. Those facing terminal illnesses will no longer have to worry about long organ waiting lists. Chinese scientists have just transplanted a modified pig liver into a brain-dead human and it seems to have worked. A less controversial approach to human organ replacement is 3D bioprinting or its 4D bioprinting iteration. These techniques involve the “printing” of a replacement organ from the stem cells of a transplant recipient, thereby eliminating the odds of organ rejection. But why stop at replacement organs when we can have “replacement humans” altogether? Future generations must think like Einsteins, be as nimble as leopards and possess owl-like night visions. And, of course, be virus-resistant as well! The manipulation of the human genome is the new “grand response” to the venerable set of “grand challenges” for 2030 and beyond. China is the go-to place for such genetic tinkering as some of these undertakings are technically illegal in the West. And this is where the utility of covid-19 comes into the picture. It provides the perfect pretext to remove such ethical constraints. After all, “Disease X” is just waiting to escape from the belly of some bat or pangolin … Since 2014, the Wuhan Institute of Virology has been the recipient of a two-stage grant worth $7.2 million from the United States government for gain-of-function research into bat coronaviruses. According to a Newsweek report in April 2020: Many scientists have criticised gain of function research, which involves manipulating viruses in the lab to explore their potential for infecting humans because it creates a risk of starting a pandemic from accidental release. Such caution has not deterred a flurry of research into microbial gene manipulation. The Wuhan experiments may have either spawned the Sars-Cov-2 virus or it may have provided a fraudulent context for future tyrannical mandates. But to solely blame China for the coronavirus “pandemic” is a tad unfair. Just as China is the factory of the world for foreign corporations, it is also the genetic incubator for a variety of viruses and chimaeras for foreign governments and foundations. Even so, the human-pig chimaera was the creation of the Salk Institute in California. Research into the world’s first human-mouse hybrid was largely a Japanese affair. The Portuguese in the meantime had created a virus chimaera. The United Kingdom, on their end, had spawned a human-cow hybrid embryo in 2008 – perhaps in keeping with the bovine disposition of those glued to the BBC. It was in Britain where the game-changing Dolly the Sheep was cloned in 1996. The transition from sheep to sheeple may turn out to be a short 21st century Jurassic Park ride. Coincidences and Consequences Before the advent of gene-editing tools and supercomputing, it would have been impossible to create a viable chimaera. The Biotech-Industrial Complex and contact tracing-type panopticons constitute a new growth area for Tech Titans that were once facing bankruptcy. The dangers of genome editing were in fact included in the Worldwide Threat Assessment reports submitted to the United States Congress in 2016 and 2017. These risks were either omitted or glossed over in the 2018 and 2019 reports – just as such risks gravitated to the high impact-high likelihood quadrant. Is it a coincidence that the nations most affected by covid-19 – at least during the first two years of its alleged spread – were the very ones that had either promoted or encouraged a variety of genetic experimentations that are contrary to nature? If – and that is a big “if” – these nations succeed in their quest for “designer babies” and “superhumans,” the rest of mankind will be rendered redundant. Some mass extermination event may transpire under the guise of World War III, food shortages, Disease X or a combination thereof. If everything goes according to plan, however, there will be 500 million potential specimens left for The Great Reset. The Third World, whose leaders are being monetarily incentivised to focus on unattainable Sustainable Development Goals (“SDGs”), will be consigned to the ash heaps of history. It is quite ironic that a new generation of cerebrally deficient “thought leaders” and “experts” are being groomed to promote the demises of their societies and themselves. About the Author Mathew Maavak, with a PhD in Policy Studies, specialises in systems science, global risks, strategic foresight, geopolitics and governance. He is a Malaysian expert on risk foresight and governance. Dr. Maavak has published numerous op-eds on a variety of eclectic subjects for over 20 years – by ‘connecting the dots’ in a disjointed world. He is the author of a Substack page titled ‘The Eye Opener’ which you can subscribe to and follow HERE. https://expose-news.com/2024/03/20/chimaeras-and-interspecies-hybrids/
    EXPOSE-NEWS.COM
    Chimaeras and interspecies hybrids; the sinister agenda hiding behind covid
    There is something that has quietly slipped through the din of the murderously phoney episode called covid-19, Dr. Mathew Maavak writes. “If the covid-19 vaccines were ‘experimental gene therapies…
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  • Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab
    Ronny Reyes
    COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.”

    Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology.

    He cited evidence found in a 2018 document from the lab that talked of making such a virus.

    Advertisement

    “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade.

    Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was man-made. 4
    Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was manmade. Rutgers New Brunswick
    The papers from the lab cited by Ebright contained drafts and notes regarding a grant proposal called Project DEFUSE, which sought to test engineering bat coronaviruses in a way that would make them more easily transmissible to humans.

    The proposal was ultimately rejected and denied funding by the US Defense Advanced Research Projects Agency, but Wade suggested that their work could have been carried out by researchers in Wuhan who had secured Chinese government funding.

    Advertisement

    “Viruses made according to the DEFUSE protocol could have been available by the time Covid-19 broke out, sometime between August and November 2019,” wrote Wade, a former science editor of the New York Times.

    Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. 4
    Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. AFP via Getty Images
    “This would account for the otherwise unexplained timing of the pandemic along with its place of origin.”

    Along with the research notes, Wade claimed the specific genetic structure of the coronavirus that allowed it to infect humans served as another strong indication of “the virus’s laboratory birth.”

    Advertisement

    “Whereas most viruses require repeated tries to switch from an animal host to people, SARS-CoV-2 infected humans out of the box, as if it had been preadapted while growing in the humanized mice called for in the DEFUSE protocol,” Wade wrote.

    While scientists continue to debate whether the coronavirus pandemic was a natural occurrence or manmade, Ebright believed there was credibility that the work proposed by the now-controversial EcoHealth Alliance led to the development COVID-19.

    Following the release of the 2018 documents — which were published by US Right to Know through a Freedom of Information Act request — Ebright said there was clearer evidence that the virus was manufactured in a lab, the Daily Telegraph reported.

    Advertisement

    The 2018 documents contained drafts and notes regarding Project DEFUSE and how to synthesize bat coronaviruses to make them more transmissible.

    The Wuhan Institute of Virology stands at the center of scrutiny over the origins of Covid-19. 4
    The Wuhan Institute of Virology stands at the center of scrutiny over the origins of COVID-19. AFP via Getty Images
    The researchers proposed introducing “appropriate human-specific cleavage sites” to the spike proteins of SARS-related viruses in the lab, the same method several biologists have said could have been used to synthesize the coronavirus that led to the pandemic.

    According to the documents, the researchers had planned to conduct a portion of the research at the Wuhan lab where they noted that safety conditions were not up to US standards, to the point where they claimed American scientists would “likely freak out.”

    Advertisement

    A spokesperson for EcoHealth Alliance said its research played no role in the start of the COVID-19 pandemic.

    “Documents representing incomplete or early drafts of the proposal have been acquired via the Freedom of Information Act and published along with allegations regarding their intent. These allegations are false, based on misunderstanding of edits and comments on the document, and based on misleading out-of-context quotations, and a lack of understanding of the process by which federal grants are awarded,” the spokesperson said.

    “Because the work was not selected for funding, any assertions about these details are by definition based on review of incomplete information and are extremely misleading.”

    Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London. 4
    Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, called on scientists to follow more rigorous safety standards. King College London
    Advertisement

    While COVID-19’s origins remain a mystery, Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, said the world needed to acknowledge that the possibility exists that the virus was synthesized.

    Speaking before the UN in New York on Wednesday, Lentzos presented the work of the Independent Task Force on Research with Pandemic Risks, which calls on scientists the world over to follow stricter regulations lest another worldwide breakout occur, the Telegraph reported.

    “We have to acknowledge the fact that the pandemic could have started from some research-related incident,” Lentzos said.

    Advertisement

    “Are we going to find that out? In my view, I think it’s very unlikely that we will. We need to do better in the future,” she added.

    “We are going to see more ambiguous events.”


    https://nypost.com/2024/02/29/world-news/scientists-may-have-started-the-covid-pandemic-article/


    https://telegra.ph/Scientist-claims-smoking-gun-evidence-COVID-19-intentionally-created-by-researchers-in-Chinese-lab-03-11
    Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab Ronny Reyes COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.” Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology. He cited evidence found in a 2018 document from the lab that talked of making such a virus. Advertisement “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade. Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was man-made. 4 Richard H. Ebright, a molecular biologist at Rutgers University, says there is enough evidence to suggest the pandemic was manmade. Rutgers New Brunswick The papers from the lab cited by Ebright contained drafts and notes regarding a grant proposal called Project DEFUSE, which sought to test engineering bat coronaviruses in a way that would make them more easily transmissible to humans. The proposal was ultimately rejected and denied funding by the US Defense Advanced Research Projects Agency, but Wade suggested that their work could have been carried out by researchers in Wuhan who had secured Chinese government funding. Advertisement “Viruses made according to the DEFUSE protocol could have been available by the time Covid-19 broke out, sometime between August and November 2019,” wrote Wade, a former science editor of the New York Times. Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. 4 Virologist Zhengli Shi, a researcher of coronavirus in bats at the Wuhan facility, was on the team seeking to engineer a virus that was more easily transmissible to humans. AFP via Getty Images “This would account for the otherwise unexplained timing of the pandemic along with its place of origin.” Along with the research notes, Wade claimed the specific genetic structure of the coronavirus that allowed it to infect humans served as another strong indication of “the virus’s laboratory birth.” Advertisement “Whereas most viruses require repeated tries to switch from an animal host to people, SARS-CoV-2 infected humans out of the box, as if it had been preadapted while growing in the humanized mice called for in the DEFUSE protocol,” Wade wrote. While scientists continue to debate whether the coronavirus pandemic was a natural occurrence or manmade, Ebright believed there was credibility that the work proposed by the now-controversial EcoHealth Alliance led to the development COVID-19. Following the release of the 2018 documents — which were published by US Right to Know through a Freedom of Information Act request — Ebright said there was clearer evidence that the virus was manufactured in a lab, the Daily Telegraph reported. Advertisement The 2018 documents contained drafts and notes regarding Project DEFUSE and how to synthesize bat coronaviruses to make them more transmissible. The Wuhan Institute of Virology stands at the center of scrutiny over the origins of Covid-19. 4 The Wuhan Institute of Virology stands at the center of scrutiny over the origins of COVID-19. AFP via Getty Images The researchers proposed introducing “appropriate human-specific cleavage sites” to the spike proteins of SARS-related viruses in the lab, the same method several biologists have said could have been used to synthesize the coronavirus that led to the pandemic. According to the documents, the researchers had planned to conduct a portion of the research at the Wuhan lab where they noted that safety conditions were not up to US standards, to the point where they claimed American scientists would “likely freak out.” Advertisement A spokesperson for EcoHealth Alliance said its research played no role in the start of the COVID-19 pandemic. “Documents representing incomplete or early drafts of the proposal have been acquired via the Freedom of Information Act and published along with allegations regarding their intent. These allegations are false, based on misunderstanding of edits and comments on the document, and based on misleading out-of-context quotations, and a lack of understanding of the process by which federal grants are awarded,” the spokesperson said. “Because the work was not selected for funding, any assertions about these details are by definition based on review of incomplete information and are extremely misleading.” Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London. 4 Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, called on scientists to follow more rigorous safety standards. King College London Advertisement While COVID-19’s origins remain a mystery, Dr. Filippa Lentzos, an associate professor of science and international security at King’s College London, said the world needed to acknowledge that the possibility exists that the virus was synthesized. Speaking before the UN in New York on Wednesday, Lentzos presented the work of the Independent Task Force on Research with Pandemic Risks, which calls on scientists the world over to follow stricter regulations lest another worldwide breakout occur, the Telegraph reported. “We have to acknowledge the fact that the pandemic could have started from some research-related incident,” Lentzos said. Advertisement “Are we going to find that out? In my view, I think it’s very unlikely that we will. We need to do better in the future,” she added. “We are going to see more ambiguous events.” https://nypost.com/2024/02/29/world-news/scientists-may-have-started-the-covid-pandemic-article/ https://telegra.ph/Scientist-claims-smoking-gun-evidence-COVID-19-intentionally-created-by-researchers-in-Chinese-lab-03-11
    NYPOST.COM
    Scientist claims ‘smoking gun’ evidence COVID-19 intentionally created by researchers in Chinese lab
    Covid-19 may have been created by a “research-related incident,” a British professor told the UN Wednesday, with Richard H. Ebright, a molecular biologist at Rutgers University, claimin…
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  • Scientist Claims ‘Smoking Gun’ Evidence Covid-19 Intentionally Created By Researchers In Chinese Lab

    COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.”

    Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology.

    He cited evidence found in a 2018 document from the lab that talked of making such a virus.

    “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade.

    SOURCE: New York Post

    Join https://t.me/RogerHodkinson
    Scientist Claims ‘Smoking Gun’ Evidence Covid-19 Intentionally Created By Researchers In Chinese Lab COVID-19 may have been created in a Chinese lab, a British professor told the UN Wednesday, with another expert claiming that evidence of the likelihood has reached “the level of a smoking gun.” Richard H. Ebright, a molecular biologist at Rutgers University, was quoted saying in a new Wall Street Journal article that the virus that killed millions around the world may actually have been manmade in China’s Wuhan Institute of Virology. He cited evidence found in a 2018 document from the lab that talked of making such a virus. “[The document] elevates the evidence provided by the genome sequence from the level of noteworthy to the level of a smoking gun,” Ebright said in the piece by former New York Times editor Nicholas Wade. SOURCE: New York Post Join πŸ‘‰ https://t.me/RogerHodkinson
    T.ME
    Dr Roger Hodkinson
    Dr Roger Hodkinson is the CEO of Western Medical Assessments, and has been the Company’s Medical Director for over 20 years.
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  • CMNnews -- Your Credible Medical News Network -- Update 27th February 2024
    From Global sources -- Updated Twice Weekly -- CMNNEWS -- We roam the planet for the best Medical News Stories

    CMNnews
    THE DOCTORS

    MONKEY NOT SEE — MONKEY NOT HEAR — MONKEY NOT SPEAK


    HISTORIC AUSTRALIAN SUPREME COURT DECISION

    STATE GOVERNMENT FOUND “ACTED UNLAWFULLY”

    IN REGARD TO VACCINE MANDATES ON POLICE AND AMBULANCE WORKERS

    Supreme Court bombshell: Queensland’s mandatory Covid vaccine orders ‘unlawful’

    Excerpts: Dozens of police and health workers have won a mammoth legal battle over mandatory Covid vaccination orders.

    Vanda Carson court reporter Courier Mail Newspaper Queensland, Australia

    2 min read

    In a 115-page decision handed down by Justice Glenn Martin on Tuesday he declared police commissioner Katarina Carroll’s direction for mandatory Covid-19 vaccination issued in December 2021 was unlawful under the Human Rights Act and banned her from taking any steps to enforce the direction.

    He also ruled that a similar order by John Wakefield, the director general of Queensland Health’s equivalent vaccination policy “is of no effect” and Mr Wakefield be blocked from forcing paramedics to have the injection.

    The workers did not have to be vaccinated while their legal fight was underway.

    Ms Carroll and Mr Wakefield are also banned from disciplining any of the paramedics and police officers.

    “I am not satisfied that the (police) Commissioner has demonstrated that she gave proper consideration to the human rights that might have been affected by her decisions,” Justice Martin said in relation to the police staff.

    “I do not accept that the Commissioner had … considered whether the decision would be compatible with human rights,” he noted in his 115-page decision.

    “By failing to give proper consideration, the making of each of those decisions was unlawful.

    “Despite the revocation of the QPS Directions, a finding of unlawfulness is still available.”

    Link: https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb

    Share CMNNews -- The Credible Medical News Network

    Update Article: Supreme Court bombshell: Qld’s mandatory Covid vaccine orders ‘unlawful’

    Excerpts: Dozens of police and health workers including paramedics have won a mammoth legal battle over mandatory ­vaccination orders after the Supreme Court declared they were unlawful.

    A spokeswoman for the Nurses’ Professional Association of Queensland (NPAQ) said the Supreme Court ruling “ highlighted how Queensland Health has violated thousands of healthcare workers’ rights”.

    The association highlighted that during a workforce crisis there were members who were stood due to the vaccine mandate who are dying to return to work.

    “We have nurses and midwives sitting at home during a workforce crisis and the healthcare system’s unlawful decisions are directly to blame,” the spokeswoman said.

    “NPAQ is currently liaising with our legal team to explore legal avenues for our members in light of today’s Supreme Court outcome.”

    https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb

    COVID-19 vaccine mandates 'unlawful' for emergency services, court finds

    The court on Tuesday delivered its judgments in three lawsuits brought by 86 parties against Queensland Police Service and Queensland Ambulance Service for their directions to workers issued in 2021 and 2022.

    The court found Police Commissioner Katarina Carroll failed to give proper consideration to human rights relevant to the decision to issue the vaccine mandate.

    “The court also found the directions limited the human rights of workers because they were required to undergo a medical procedure without full consent ….”

    Australian Senate finally acknowledge excess deaths are concerning : Letter from Australian Senator Ralph Babet

    SENATOR RALPH BABET — IS THIS THE GREATEST SENATE DECISION IN HISTORY? TWO MINUTE VIDEO



    JIM FERGUSON – “THIS IS GENOCIDE – MURDER OF MILLIONS AND POSSIBLY BILLIONS OF PEOPLE” – “THE PRIME MINISTER COULD BE INVOLVED” -- “THESE ARE CRIMES AGAINST HUMANITY”

    “Explosive allegations against top Government officials in the UK Government update. As Member of Parliament Andrew Bridgen prepares to present evidence of potential criminal conduct involving Prime Minister Rishi Sunak and his cabinet to London's Metropolitan Police Commissioner Mark Rowley, we explore the mindset of others who might be implicated in alleged widespread wrongdoing, including potential mass genocide and profiteering. Will they now do the right thing and blow the lid on whats really been going on! If the gatekeepers in our Security Services and Police are compromised or complicit in what is arguably the greatest potential crime against humanity of all time then all bets are off as to what happens next.”

    https://twitter.com/i/status/1761505188056072263

    DR DAVID MARTIN EXPLAINS WHO THEY ARE AND HOW THEY ARE DOING THIS TO US


    “THEY WERE CONVICTED OF ANTI-TRUST CRIMES”

    “THIS IS A CRIMINAL CONSPIRACY”

    “WHO IS MOVING THE STICK – WELLCOME, GATES AND ROCKEFELLER”

    “THIS IS A VIOLATION OF SWISS LAW”

    Dr. David Martin Reveals Who Is Pulling the Strings Behind the World Health Organization

    Who are “THEY”? “We have to name the names” in the worst miscarriage of medical science in history. Is it the World Health Organization? Dr. David Martin says Tedros is just a puppet with a “giant stick up his ass, which is what’s making his mouth move…

    18 days ago · 446 likes · 136 comments · The Vigilant Fox

    BILL GATES DONATION TO WORLD HEALTH ORGANIZATION


    JIM FERGUSON INTERVIEWS ANDREW BRIDGEN --

    “Exclusive Breaking News: Evidence to be presented that criminal activity has been committed by the very top of Government in the UK. Rishi Sunak British Prime Minister may face a criminal investigation and face potential criminal charges of the most egregious kind. British MP Andrew Bridgen has written to Mark Rowley Commissioner of the Metropolitan Police and the most senior of Police officers to have a three hour meeting where experts and whistle blowers will lay out the evidence where potential criminal activity has been conducted by the very top of Government and the civil service in the UK Parliament has been deliberately misled over the vaccine contracts. This matter may be taken to Parliamentary standards in addition to the presentation of evidence to the Police and the Security services. "heads of governments around the world and others below them have engaged in what is tantamount to treason against the public" Office of National Statistics (ONS) figures on Excess Deaths are being covered up. "there is a huge coverup going on" In August 2019 a member of the security services stated that there was a pandemic coming and not to take any of the vaccines. Bill gates and Rishi Sunak invested heavily into the Pharma companies like Pfizer and Moderna prior to the pandemic. Did they have insider knowledge about what was being planned in a coming pandemic! 75% of congressmen and woman in the United States have investments in Big Pharma. A Pfizer executive stated that a senator could be bought for $10,000. The journalists are complicit in the cover up. Main Stream Media are bought and paid for. A court case has been launched against the former health secretary Matt Hancock for defamation against Andrew Bridgen and this will take place in the Royal Court of Justice.”

    https://twitter.com/i/status/1761393940874293335

    THESE EVIL PEOPLE ARE COMING AFTER OUR PETS – YOUR DOGS AND CATS – A SECURITY CHIEF WARNED “DO NOT TAKE THE VACCINE” – “THE PRIME MINISTER OF THE UK, RISHI SUNAK, INVESTED HALF A BILLION DOLLARS INTO MODERNA TWO TO THREE YEARS BEFORE COVID OCCURRED” – “HE MUST HAVE HAD PRIOR KNOWLEDGE”

    https://rumble.com/v4ew676-these-evil-monsters-are-coming-after-our-pets.html


    JIM FERGUSON ON TWITTER

    @JimFergusonUK

    “British PM and #WEF2030Agenda devotee #Sunak invested $500 million of his private funds into Moderna through a company called Thelema Partners in a notorious tax haven in the Caymen Islands. Afterwards he stated in parliament that the vaccine was "safe and effective" while then going on to roll out further permissions for Moderna to set up further vaccine producing interests within the UK. Did he use his position as Prime Minister to make massive personal profits while knowingly or even unknowingly causing harm to the British people and has he broken the National Security Act which states "if you're working in secret for a foreign power to use or abuse your knowledge in a way that causes harm to our citizens you will be a criminal." Former Head of MI6 Sir Alex Younger.”

    2024 Is the Last Year of Free Speech and Democracy in the Western World

    https://www.paulcraigroberts.org/2024/02/19/2024-is-the-last-year-of-free-speech-and-democracy-in-the-western-world/


    To Understand The Globalists We Must Understand Their Psychopathic Religion

    https://alt-market.us/to-understand-the-globalists-we-must-understand-their-psychopathic-religion/

    TWO BRAVE AND COURAGEOUS DOCTORS

    #141 - Dr Charles Hoffe, A Persecuted Ethical Doctor Or Dangerous Misinformation Spreader?

    FREEDOM - LIBERTY - HAPPINESS SUPPORT DOC MALIK About this conversation - Dr Charles Hoffe is a family doctor who lives and works in British Columbia, Canada. He has worked in general practice and emer…

    14 days ago · 34 likes · 5 comments · Doc Malik

    New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023)

    VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023)

    VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023…

    14 days ago · 122 likes · 57 comments · Dr. William Makis MD

    LIST OF LAWYERS NOW AVAILABLE FOR LAWSUITS ON COVID VACCINE INJURY

    https://deeprootsathome.com/list-of-attorneys-worldwide-now-available-for-lawsuits/


    Kaboom! — Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3

    "We've just seen this in the last 2 years... but we didn’t see this before the vaccines. The doctor noticed this between two years to one year ago, in about 50% of the patients,"

    Kaboom! Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3

    It’s taking a long time folks, but the worms are crawling out of the cans, and corrupt institutions and politicians are scrambling to seal them back in! Perhaps due to a significant decrease in mRNA vaccine sales influencing pharmaceutical companies…

    18 days ago · 103 likes · 30 comments · Aussie17

    mRNA VACCINE SHEDDING OF SPIKE PROTEIN

    As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s 2015 document on Gene Product Shedding Studies and all other gene therapy products on the market list shedding as a risk in their [package] insert (Luxterna, Roctavian, Zolgensma) and shed from 7 days to 6 months.”

    phillip.altman’s Substack

    mRNA VACCINE SHEDDING OF SPIKE PROTEIN There has been considerable concern about the potential for the vaccinated to shed Spike Protein to the unvaccinated. See Dr. Piere Kory’s Substack of 20 Feb. CLICK HERE to view. As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s…

    Read more

    18 days ago · 64 likes · 9 comments · phillip.altman

    WORLDWIDE CENSORSHIP IS UNDER WAY –

    “Google Isn’t Just Trying to Rewrite History. It’s at the Centre of a Worldwide Web of Censorship”

    https://dailysceptic.org/2024/02/25/google-isnt-just-trying-to-rewrite-history-its-at-the-centre-of-a-worldwide-web-of-censorship/


    TUCKER CARLSON INTERVIEW – JUST 6 MINUTES

    Steve Kirsch Tags the COVID Jab as the ‘Most Dangerous Vaccine of All Time’ The VAERS system has identified 770 safety signals related to the COVID-19 vaccine.

    “That is mind-blowing. That is not a three-alarm fire. That is a 770-alarm fire.” So, what did the CDC do? “They said nothing.”

    https://twitter.com/VigilantFox/status/1761369027685793810

    FOREIGN DNA SHOULD NOT BE IN THE VACCINES – IT CAN ENTER THE DNA IN THE NUCLEUS OF EACH CELL

    Kevin McKernan testifies about how the FDA and Regulators, funded by those who profit from the deception in a great conflict of interest, put the human genome at risk by downplaying the risk of DNA integration.

    Crimes Against Humanity Case Phase 1 Starts At The Same Time We Learn That Covid "Vaccine" DNA Integration Into Ovaries Chromosomes 19 & 12 Is Now Confirmed! Lying Health Ministers, CDC, W.H.O. OH MY!

    This video needs to go viral! SHARE! IoJ is filing an injunction to stop the shots pronto based on the evidence in this Substack article. Our Donation Drive is now open!!! We can win this! Everyone’s going down dammit. This is just unacceptable. The human genome, heritage of humanity is at risk from the WHO and regulators cow towing to Big Pharma’s covi…

    Read more

    13 days ago · 84 likes · 34 comments · Interest of Justice

    MICROPLASTICS – WHAT ARE THEY?

    Humanity United Now - Ana Maria Mihalcea, MD, PhD

    Microplastics - aka Nanotechnological Self Assembly Polymers - Are Everywhere - Poisoning Our Biosphere, Food Supply And Humans

    The use of the word microplastics is once again to normalize the self assembly polymers that have been sprayed via illegal Geoengineering and bioengineering operations to transform our biosphere according to the transhumanist agenda. This is literally killing our planet, killing all life and humanity. This microplastics cover story is to explain why the…

    Read more

    5 months ago · 141 likes · 53 comments · Ana Maria Mihalcea, MD, PhD

    TRICKS AND TREATS FOR A COVID JAB IN NEW ZEALAND

    VIDEO - New Zealand Vax Propaganda & subsequent Sudden Deaths "Get the jab, get the treats" (Oct.16, 2021 Super Saturday Vaxathon)

    VIDEO - New Zealand Vax Propaganda & Sudden Deaths "Get the jab, get the treats" (Source: Coronavirus Plushie) Get the jab, get the treats . . . Incentivizing Kiwis to get jabbed by offering them cash prizes, food, free tickets for the rugby, and other kinds of 'treats', was a big part of the 16 Oct, 2021 'Super Saturday Vaxathon…

    19 days ago · 101 likes · 65 comments · Dr. William Makis MD

    99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree.

    A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals concludes that the benefits of COVID outweigh the risks. My colleagues and I disagree.

    99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree.

    Executive summary A new study of over 99 million vaccinated people has been highly promoted in the press with headlines like “Covid Vaccines Linked To Small Increase In Heart And Brain Disorders, Study Finds—But Risk From Infection Is Far Higher.” I’m going to convince you that this is bullshit…

    Read more

    18 days ago · 525 likes · 334 comments · Steve Kirsch

    “All of the harms from the COVID-19 injectable products were predictable, and preventable”

    There are no 'desired proteins' with regard to the modified spike mRNA

    “All of the harms from the COVID-19 injectable products were predictable, and preventable.” Jessica Rose, PhD A Nature publication by Mulroney et al. entitled N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting was published on December 6, 2023. The authors showed that N1-methylpseudouridine affects the fidelity of mRNA translation via ri…

    Read more

    3 months ago · 272 likes · 67 comments · Jessica Rose

    Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians

    COVID Chronicles

    Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians

    The Epoch Times, a media outlet that is not state-funded, released an article yesterday that was updated today. Everyone around the world should read it. You can find it here. The journalist, Noé Chartier, did an excellent job writing a well-balanced, objective, and factual account. I do not have much to add…

    Read more

    15 days ago · 370 likes · 104 comments · Dr. Byram W. Bridle

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    https://open.substack.com/pub/cmnnews/p/cmnnews-your-credible-medical-news-a60?r=29hg4d&utm_medium=ios

    https://telegra.ph/CMNnews----Your-Credible-Medical-News-Network----Update-27th-February-2024-03-11
    CMNnews -- Your Credible Medical News Network -- Update 27th February 2024 From Global sources -- Updated Twice Weekly -- CMNNEWS -- We roam the planet for the best Medical News Stories CMNnews THE DOCTORS MONKEY NOT SEE — MONKEY NOT HEAR — MONKEY NOT SPEAK HISTORIC AUSTRALIAN SUPREME COURT DECISION STATE GOVERNMENT FOUND “ACTED UNLAWFULLY” IN REGARD TO VACCINE MANDATES ON POLICE AND AMBULANCE WORKERS Supreme Court bombshell: Queensland’s mandatory Covid vaccine orders ‘unlawful’ Excerpts: Dozens of police and health workers have won a mammoth legal battle over mandatory Covid vaccination orders. Vanda Carson court reporter Courier Mail Newspaper Queensland, Australia 2 min read In a 115-page decision handed down by Justice Glenn Martin on Tuesday he declared police commissioner Katarina Carroll’s direction for mandatory Covid-19 vaccination issued in December 2021 was unlawful under the Human Rights Act and banned her from taking any steps to enforce the direction. He also ruled that a similar order by John Wakefield, the director general of Queensland Health’s equivalent vaccination policy “is of no effect” and Mr Wakefield be blocked from forcing paramedics to have the injection. The workers did not have to be vaccinated while their legal fight was underway. Ms Carroll and Mr Wakefield are also banned from disciplining any of the paramedics and police officers. “I am not satisfied that the (police) Commissioner has demonstrated that she gave proper consideration to the human rights that might have been affected by her decisions,” Justice Martin said in relation to the police staff. “I do not accept that the Commissioner had … considered whether the decision would be compatible with human rights,” he noted in his 115-page decision. “By failing to give proper consideration, the making of each of those decisions was unlawful. “Despite the revocation of the QPS Directions, a finding of unlawfulness is still available.” Link: https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb Share CMNNews -- The Credible Medical News Network Update Article: Supreme Court bombshell: Qld’s mandatory Covid vaccine orders ‘unlawful’ Excerpts: Dozens of police and health workers including paramedics have won a mammoth legal battle over mandatory ­vaccination orders after the Supreme Court declared they were unlawful. A spokeswoman for the Nurses’ Professional Association of Queensland (NPAQ) said the Supreme Court ruling “ highlighted how Queensland Health has violated thousands of healthcare workers’ rights”. The association highlighted that during a workforce crisis there were members who were stood due to the vaccine mandate who are dying to return to work. “We have nurses and midwives sitting at home during a workforce crisis and the healthcare system’s unlawful decisions are directly to blame,” the spokeswoman said. “NPAQ is currently liaising with our legal team to explore legal avenues for our members in light of today’s Supreme Court outcome.” https://www.couriermail.com.au/truecrimeaustralia/police-courts-qld/supreme-court-bombshell-qlds-mandatory-covid-vaccine-orders-unlawful/news-story/4dcc6ca18dae261249fd7988642192fb COVID-19 vaccine mandates 'unlawful' for emergency services, court finds The court on Tuesday delivered its judgments in three lawsuits brought by 86 parties against Queensland Police Service and Queensland Ambulance Service for their directions to workers issued in 2021 and 2022. The court found Police Commissioner Katarina Carroll failed to give proper consideration to human rights relevant to the decision to issue the vaccine mandate. “The court also found the directions limited the human rights of workers because they were required to undergo a medical procedure without full consent ….” Australian Senate finally acknowledge excess deaths are concerning : Letter from Australian Senator Ralph Babet SENATOR RALPH BABET — IS THIS THE GREATEST SENATE DECISION IN HISTORY? TWO MINUTE VIDEO JIM FERGUSON – “THIS IS GENOCIDE – MURDER OF MILLIONS AND POSSIBLY BILLIONS OF PEOPLE” – “THE PRIME MINISTER COULD BE INVOLVED” -- “THESE ARE CRIMES AGAINST HUMANITY” “Explosive allegations against top Government officials in the UK Government update. As Member of Parliament Andrew Bridgen prepares to present evidence of potential criminal conduct involving Prime Minister Rishi Sunak and his cabinet to London's Metropolitan Police Commissioner Mark Rowley, we explore the mindset of others who might be implicated in alleged widespread wrongdoing, including potential mass genocide and profiteering. Will they now do the right thing and blow the lid on whats really been going on! If the gatekeepers in our Security Services and Police are compromised or complicit in what is arguably the greatest potential crime against humanity of all time then all bets are off as to what happens next.” https://twitter.com/i/status/1761505188056072263 DR DAVID MARTIN EXPLAINS WHO THEY ARE AND HOW THEY ARE DOING THIS TO US “THEY WERE CONVICTED OF ANTI-TRUST CRIMES” “THIS IS A CRIMINAL CONSPIRACY” “WHO IS MOVING THE STICK – WELLCOME, GATES AND ROCKEFELLER” “THIS IS A VIOLATION OF SWISS LAW” Dr. David Martin Reveals Who Is Pulling the Strings Behind the World Health Organization Who are “THEY”? “We have to name the names” in the worst miscarriage of medical science in history. Is it the World Health Organization? Dr. David Martin says Tedros is just a puppet with a “giant stick up his ass, which is what’s making his mouth move… 18 days ago · 446 likes · 136 comments · The Vigilant Fox BILL GATES DONATION TO WORLD HEALTH ORGANIZATION JIM FERGUSON INTERVIEWS ANDREW BRIDGEN -- “Exclusive Breaking News: Evidence to be presented that criminal activity has been committed by the very top of Government in the UK. Rishi Sunak British Prime Minister may face a criminal investigation and face potential criminal charges of the most egregious kind. British MP Andrew Bridgen has written to Mark Rowley Commissioner of the Metropolitan Police and the most senior of Police officers to have a three hour meeting where experts and whistle blowers will lay out the evidence where potential criminal activity has been conducted by the very top of Government and the civil service in the UK Parliament has been deliberately misled over the vaccine contracts. This matter may be taken to Parliamentary standards in addition to the presentation of evidence to the Police and the Security services. "heads of governments around the world and others below them have engaged in what is tantamount to treason against the public" Office of National Statistics (ONS) figures on Excess Deaths are being covered up. "there is a huge coverup going on" In August 2019 a member of the security services stated that there was a pandemic coming and not to take any of the vaccines. Bill gates and Rishi Sunak invested heavily into the Pharma companies like Pfizer and Moderna prior to the pandemic. Did they have insider knowledge about what was being planned in a coming pandemic! 75% of congressmen and woman in the United States have investments in Big Pharma. A Pfizer executive stated that a senator could be bought for $10,000. The journalists are complicit in the cover up. Main Stream Media are bought and paid for. A court case has been launched against the former health secretary Matt Hancock for defamation against Andrew Bridgen and this will take place in the Royal Court of Justice.” https://twitter.com/i/status/1761393940874293335 THESE EVIL PEOPLE ARE COMING AFTER OUR PETS – YOUR DOGS AND CATS – A SECURITY CHIEF WARNED “DO NOT TAKE THE VACCINE” – “THE PRIME MINISTER OF THE UK, RISHI SUNAK, INVESTED HALF A BILLION DOLLARS INTO MODERNA TWO TO THREE YEARS BEFORE COVID OCCURRED” – “HE MUST HAVE HAD PRIOR KNOWLEDGE” https://rumble.com/v4ew676-these-evil-monsters-are-coming-after-our-pets.html JIM FERGUSON ON TWITTER @JimFergusonUK “British PM and #WEF2030Agenda devotee #Sunak invested $500 million of his private funds into Moderna through a company called Thelema Partners in a notorious tax haven in the Caymen Islands. Afterwards he stated in parliament that the vaccine was "safe and effective" while then going on to roll out further permissions for Moderna to set up further vaccine producing interests within the UK. Did he use his position as Prime Minister to make massive personal profits while knowingly or even unknowingly causing harm to the British people and has he broken the National Security Act which states "if you're working in secret for a foreign power to use or abuse your knowledge in a way that causes harm to our citizens you will be a criminal." Former Head of MI6 Sir Alex Younger.” 2024 Is the Last Year of Free Speech and Democracy in the Western World https://www.paulcraigroberts.org/2024/02/19/2024-is-the-last-year-of-free-speech-and-democracy-in-the-western-world/ To Understand The Globalists We Must Understand Their Psychopathic Religion https://alt-market.us/to-understand-the-globalists-we-must-understand-their-psychopathic-religion/ TWO BRAVE AND COURAGEOUS DOCTORS #141 - Dr Charles Hoffe, A Persecuted Ethical Doctor Or Dangerous Misinformation Spreader? FREEDOM - LIBERTY - HAPPINESS SUPPORT DOC MALIK About this conversation - Dr Charles Hoffe is a family doctor who lives and works in British Columbia, Canada. He has worked in general practice and emer… 14 days ago · 34 likes · 5 comments · Doc Malik New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023) VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023) VIDEO - New Zealand COVID-19 Vaccine Victims Documentary: "Silent No More" (June 2023… 14 days ago · 122 likes · 57 comments · Dr. William Makis MD LIST OF LAWYERS NOW AVAILABLE FOR LAWSUITS ON COVID VACCINE INJURY https://deeprootsathome.com/list-of-attorneys-worldwide-now-available-for-lawsuits/ Kaboom! — Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3 "We've just seen this in the last 2 years... but we didn’t see this before the vaccines. The doctor noticed this between two years to one year ago, in about 50% of the patients," Kaboom! Renowned Neurologist and Thai Red Cross Emerging Infectious Diseases Health Science Centre Lead Prof. Dr. Thiravat Hemachudha Exposes Vaccine-Linked White Clots on Thailand's Popular TV3 It’s taking a long time folks, but the worms are crawling out of the cans, and corrupt institutions and politicians are scrambling to seal them back in! Perhaps due to a significant decrease in mRNA vaccine sales influencing pharmaceutical companies… 18 days ago · 103 likes · 30 comments · Aussie17 mRNA VACCINE SHEDDING OF SPIKE PROTEIN As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s 2015 document on Gene Product Shedding Studies and all other gene therapy products on the market list shedding as a risk in their [package] insert (Luxterna, Roctavian, Zolgensma) and shed from 7 days to 6 months.” phillip.altman’s Substack mRNA VACCINE SHEDDING OF SPIKE PROTEIN There has been considerable concern about the potential for the vaccinated to shed Spike Protein to the unvaccinated. See Dr. Piere Kory’s Substack of 20 Feb. CLICK HERE to view. As Dr. Kory points out, “COVID “vaccines” are gene therapy products as defined in the FDA’s… Read more 18 days ago · 64 likes · 9 comments · phillip.altman WORLDWIDE CENSORSHIP IS UNDER WAY – “Google Isn’t Just Trying to Rewrite History. It’s at the Centre of a Worldwide Web of Censorship” https://dailysceptic.org/2024/02/25/google-isnt-just-trying-to-rewrite-history-its-at-the-centre-of-a-worldwide-web-of-censorship/ TUCKER CARLSON INTERVIEW – JUST 6 MINUTES Steve Kirsch Tags the COVID Jab as the ‘Most Dangerous Vaccine of All Time’ The VAERS system has identified 770 safety signals related to the COVID-19 vaccine. “That is mind-blowing. That is not a three-alarm fire. That is a 770-alarm fire.” So, what did the CDC do? “They said nothing.” https://twitter.com/VigilantFox/status/1761369027685793810 FOREIGN DNA SHOULD NOT BE IN THE VACCINES – IT CAN ENTER THE DNA IN THE NUCLEUS OF EACH CELL Kevin McKernan testifies about how the FDA and Regulators, funded by those who profit from the deception in a great conflict of interest, put the human genome at risk by downplaying the risk of DNA integration. Crimes Against Humanity Case Phase 1 Starts At The Same Time We Learn That Covid "Vaccine" DNA Integration Into Ovaries Chromosomes 19 & 12 Is Now Confirmed! Lying Health Ministers, CDC, W.H.O. OH MY! This video needs to go viral! SHARE! IoJ is filing an injunction to stop the shots pronto based on the evidence in this Substack article. Our Donation Drive is now open!!! We can win this! Everyone’s going down dammit. This is just unacceptable. The human genome, heritage of humanity is at risk from the WHO and regulators cow towing to Big Pharma’s covi… Read more 13 days ago · 84 likes · 34 comments · Interest of Justice MICROPLASTICS – WHAT ARE THEY? Humanity United Now - Ana Maria Mihalcea, MD, PhD Microplastics - aka Nanotechnological Self Assembly Polymers - Are Everywhere - Poisoning Our Biosphere, Food Supply And Humans The use of the word microplastics is once again to normalize the self assembly polymers that have been sprayed via illegal Geoengineering and bioengineering operations to transform our biosphere according to the transhumanist agenda. This is literally killing our planet, killing all life and humanity. This microplastics cover story is to explain why the… Read more 5 months ago · 141 likes · 53 comments · Ana Maria Mihalcea, MD, PhD TRICKS AND TREATS FOR A COVID JAB IN NEW ZEALAND VIDEO - New Zealand Vax Propaganda & subsequent Sudden Deaths "Get the jab, get the treats" (Oct.16, 2021 Super Saturday Vaxathon) VIDEO - New Zealand Vax Propaganda & Sudden Deaths "Get the jab, get the treats" (Source: Coronavirus Plushie) Get the jab, get the treats . . . Incentivizing Kiwis to get jabbed by offering them cash prizes, food, free tickets for the rugby, and other kinds of 'treats', was a big part of the 16 Oct, 2021 'Super Saturday Vaxathon… 19 days ago · 101 likes · 65 comments · Dr. William Makis MD 99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree. A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals concludes that the benefits of COVID outweigh the risks. My colleagues and I disagree. 99 million patient records and they concluded that the benefits outweigh the risks!?!? We respectfully disagree. Executive summary A new study of over 99 million vaccinated people has been highly promoted in the press with headlines like “Covid Vaccines Linked To Small Increase In Heart And Brain Disorders, Study Finds—But Risk From Infection Is Far Higher.” I’m going to convince you that this is bullshit… Read more 18 days ago · 525 likes · 334 comments · Steve Kirsch “All of the harms from the COVID-19 injectable products were predictable, and preventable” There are no 'desired proteins' with regard to the modified spike mRNA “All of the harms from the COVID-19 injectable products were predictable, and preventable.” Jessica Rose, PhD A Nature publication by Mulroney et al. entitled N1-methylpseudouridylation of mRNA causes +1 ribosomal frameshifting was published on December 6, 2023. The authors showed that N1-methylpseudouridine affects the fidelity of mRNA translation via ri… Read more 3 months ago · 272 likes · 67 comments · Jessica Rose Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians COVID Chronicles Health Canada Hid Their Concerns About Impurities In COVID-19 Shots From Canadians The Epoch Times, a media outlet that is not state-funded, released an article yesterday that was updated today. Everyone around the world should read it. You can find it here. The journalist, Noé Chartier, did an excellent job writing a well-balanced, objective, and factual account. I do not have much to add… Read more 15 days ago · 370 likes · 104 comments · Dr. Byram W. Bridle Subscribe to CMNNews - The Credible Medical News Network News From Around the Globe -- Updated Twice Weekly Disclaimer: All content is presented for educational and/or entertainment purposes only. 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  • BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome
    2nd Smartest Guy in the World
    This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered.

    Any type of integration into the genome, especially when being assaulted by millions of different random sequences from the “vaccine,” will inevitably cause mutations and other damage to the genome, irrespective if the entire spike protein is expressed, or not.

    This DNA contamination ultimately results in the plethora of slow kill bioweapon adverse events that we are now seeing in surging amounts, not limited to prion diseases, turbo cancers, SADS, and so on and so forth.

    The below is translated from Japanese, and it is a rather technical read, but well worth your time.


    by Mao Arakawa (Okudo Hirokushi)

    The essence of the corona vaccine contaminated DNA problem is the possibility of altering the human genome. To validate this possibility, Dr. Ulrike Kaemmerer conducted an experiment to administer the corona vaccine to MCF7 and OVCAR-3 cancer cell lines. Dr. McKernan, consulted by Dr. Kaemmerer, conducted an experiment to detect contaminated DNA from these cell lines. He reports on his blog the first case of contaminated DNA integration into the cancer cell line genome. (2SG: yesterdays article entitled, UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases addresses this.)

    I was interested, so I attempted to recreate the DNA recombinant event that Dr. McKernan identified. In this article, I will show the results of my analysis.

    Nepetalactone Newsletter

    Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2

    Ulrike Kaemmerer has treated MCF7 and OvCar3 cancer cell lines with various vaccines. Once transfected they performed cell passaging on these transfected cell lines to dilute out the residual vaccine and identify cells which were transfected. They performed Immunohistochemistry (IHC) on these cells and documented spike expression levels…

    Read more

    14 days ago · 109 likes · 22 comments · Anandamide

    image
    Figure 1
    Dr. Kaemmerer administered the corona vaccine from Pfizer and AstraZeneca to the ovarian tumor cell line OVCAR-3 and, after subculture, confirmed the expression of the spikutanpak by immunohistochemical staining. Deep Sequencing comes at a high cost; therefore, preliminary experiments are required in advance to perform DNA detection experiments. Dr. McKernan first screened post-vaccination cells with qPCR and targeted qPCR-positive cells for deep sequencing.

    Contaminated DNA that is not integrated into the genome is diluted with subculture. In fact, the Ct value of the vector was Ct 30.28 in the first generation, but it was 34.72 in the second generation. The difference in 4Ct is 16 times the difference, and that is the lower concentration in the second passage. Dr. McKernan extracted DNA from two cells subcultured and performed deep sequencing. Sequence data detected SV40, replication origin and spiked DNA. Spike DNA was detected in the full genomic shotgun library of vaccine-treated samples with 3000x coverage. (Coverage means the percentage of the total base pair or locus of the genome covered by sequencing.) Since the coverage in the human genome was 30 times, we can see that the DNA with a large number of copies of the genome was invading the cell.

    As a result, strangely, SNP (monobasic polymorphism) was detected in deep sequencing at the origin of the vaccine plasmid replication (F1 and SV40). This SNP does not exist in the vaccine. In other words, it seems that plasmids are mutating in cells. Also, the coverage of deep sequencing in the replication origin area is higher than average, and the number of copies observed is relatively high, which means that the DNA embedded in the cell may be duplicated and mutated. I mean. Originally, plasmids and SV40 DNA replication require specific enzymes not owned by human cells. Experiments such as the introduction of large amounts of microDNA fragments containing replication points into cells are not usually performed in molecular genetics. It is possible that unexpected DNA replication is occurring within the cell.

    A total of two genomic integrations were observed in the vaccinated cell line from the analysis of Deep Sequencing by Dr. McKernan. Individual arrays of deep sequencing are called γ€Œ leads 」. It was very interesting data, so I tried to re-parse the lead myself.

    image
    Figure 2
    Figure 2 is a lead showing genomic integration in Dr. McKernan's Deep Sequencing Analysis. The subject of the analysis is Genome Integration Leads 1 and 2. You can also read a lot of information from short array data. This time in comparison with the human genomeblat searchTo find homologyblast searchI used it.

    Now, after that, it will be my own re-parse.

    image
    Figure 3
    The top of the array in Figure 3 is the lead. As you can tell by aligning this lead with the 12th chromosome (black) and the spike gene (red) of the Pfizer Corona vaccine, the 12th chromosome (black) is on the way to the spike gene (red). I am switching. And there is a short identical array (here GAGAG) in the place of switching. You can see that the end-recombination (MMEJ, Microhomology-mediated end joining) mediated by microhomology (microhomology) recombinates the contaminated DNA and human genome. Since MMEJ involves multiple intracellular DNA repair enzymes, this recombination is an artifact (mistake product) in the test tube. Instead, gene recombination may have occurred in cells.

    Genome integration occurs on the long arm of chromosome 12, and the FAIM2 gene is present at this locus. FAIM2 is a gene that has been suggested to be associated with cancer malignancy. Recombinations occur on introns (arrays that do not encode proteins), but I do not know how such mutations also affect gene expression.

    image
    Figure 4
    Another example of genomic integration is Figure 4. If you align this lead with chromosome 9 (black) and spike gene (red), you can see that in the lead, chromosome 9 (black) is switching to the spike gene (red) on the way. There is a short identical array (here TCTGCCCT) in the place where this example also switches. After all, it is believed that the contaminated DNA and the human genome were recombined using microhomology. Since there are multiple pathways for DNA repair, which repair pathway is used when foreign DNA is taken into the genome is case-by-case.

    Part of the lead had an Illumina adapter array left. Adapter arrays are arrays granted to PCR amplify and sequence DNA for deep sequencing. Originally, the adapter array is removed during parsing, but often the removal is inadequate and remains in the lead.

    Integration of contaminated DNA into the genome is occurring near Centromea. Let's talk a little about Centromea. Two chromosomes with the same genetic information that can be done after DNA replication are chromatids (sister chromatids). The chromatids are connected until the chromosomes are distributed during cell division, but the region on the connected DNA is Centromea. As such, Centromea is an important area for chromosome separation and distribution.

    image
    Figure 5
    Figure 5 is about the DNA fragments of the spike gene integrated into the genome. On the Pfizer Corona vaccine spike gene, the sequence found in the genome integrated lead was written in red. Due to lead length limitations, the actual integrated array will be even larger. The integrated sequence is part of the spike gene, and it is not possible to make a full-length spike sequence. However, it is unpredictable how contaminated DNA will be inserted into any area of the genome and have any effect.

    image
    Figure 6
    Nucleotype (cario type) means the size, shape, and number of chromosomes. Human chromosomes consist of a total of 46 22 pairs of autosomal and one pair of sex chromosomes. The autosomal is assigned the number 1 chromosome, number 2 chromosome,, number 22 chromosome and number in order of size. The integrated site of contaminated DNA is the FAIM2 locus on the long arm of chromosome 9 and near Centromea on chromosome 12.

    The genomic integration observed this time is the first two cases in cultured cell experiments, but the specific identification of recombinant sequences with the human genome of contaminated DNA is a major advance. Further verification experiments will be advanced in the future. Genome integration, as in Figure 6, does not know which locus actually occurs on the genome. This is exactly the γ€Œ shotgun attack on the genome 」. What happens in cultured cells can also occur in normal cells, with a wide variety of alterations depending on the site of genomic integration. The first predicted catabolism is cancer induction and malignancy. And then, the ones that manifest themselves over time are various genetic diseases.

    What is known as a factor that causes genomic damage is, for example, radiation exposure, but genomic modification by contaminated DNA is different in that it is due to fragments of artificially created genes, and random mutations which are akin to radiation. But it is fundamentally different in nature. This experiment in cultured cells epitomizes genomic integration of contaminated DNA. This is a real problem that a large number of humans around the world, under the name of vaccination, are now experiencing aγ€Œ transfection human body experiment 」of contaminated DNA.

    The genomic modification of humanity is a direct consequence of the largest experiment in history of mRNA drug substance harm, and in the future it may be etched in history as theγ€Œ original sin 」of humanity.


    Original Social Engineering Sin

    Original Social Engineering Sin
    “...the socio-psychological foundations of socialism is identical to that of the foundations of a state, if there were no institution enforcing socialistic ideas of property, there would be no room for a state, as a state is nothing else than an institution built on taxation and unsolicited, noncontractual interference with the use that private people c…

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    BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome




    https://www.2ndsmartestguyintheworld.com/p/breaking-integration-of-corona-vaccine

    https://telegra.ph/BREAKING-Integration-of-corona-vaccine-contaminated-DNA-into-the-human-cell-line-genome-03-11
    BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 2nd Smartest Guy in the World This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered. Any type of integration into the genome, especially when being assaulted by millions of different random sequences from the “vaccine,” will inevitably cause mutations and other damage to the genome, irrespective if the entire spike protein is expressed, or not. This DNA contamination ultimately results in the plethora of slow kill bioweapon adverse events that we are now seeing in surging amounts, not limited to prion diseases, turbo cancers, SADS, and so on and so forth. The below is translated from Japanese, and it is a rather technical read, but well worth your time. by Mao Arakawa (Okudo Hirokushi) The essence of the corona vaccine contaminated DNA problem is the possibility of altering the human genome. To validate this possibility, Dr. Ulrike Kaemmerer conducted an experiment to administer the corona vaccine to MCF7 and OVCAR-3 cancer cell lines. Dr. McKernan, consulted by Dr. Kaemmerer, conducted an experiment to detect contaminated DNA from these cell lines. He reports on his blog the first case of contaminated DNA integration into the cancer cell line genome. (2SG: yesterdays article entitled, UPDATE: Doctors Warn mRNA "Vaccines" Could Spur Epidemic of Prion Brain Diseases addresses this.) I was interested, so I attempted to recreate the DNA recombinant event that Dr. McKernan identified. In this article, I will show the results of my analysis. Nepetalactone Newsletter Vaccine targeted qPCR of Cancer Cell Lines treated with BNT162b2 Ulrike Kaemmerer has treated MCF7 and OvCar3 cancer cell lines with various vaccines. Once transfected they performed cell passaging on these transfected cell lines to dilute out the residual vaccine and identify cells which were transfected. They performed Immunohistochemistry (IHC) on these cells and documented spike expression levels… Read more 14 days ago · 109 likes · 22 comments · Anandamide image Figure 1 Dr. Kaemmerer administered the corona vaccine from Pfizer and AstraZeneca to the ovarian tumor cell line OVCAR-3 and, after subculture, confirmed the expression of the spikutanpak by immunohistochemical staining. Deep Sequencing comes at a high cost; therefore, preliminary experiments are required in advance to perform DNA detection experiments. Dr. McKernan first screened post-vaccination cells with qPCR and targeted qPCR-positive cells for deep sequencing. Contaminated DNA that is not integrated into the genome is diluted with subculture. In fact, the Ct value of the vector was Ct 30.28 in the first generation, but it was 34.72 in the second generation. The difference in 4Ct is 16 times the difference, and that is the lower concentration in the second passage. Dr. McKernan extracted DNA from two cells subcultured and performed deep sequencing. Sequence data detected SV40, replication origin and spiked DNA. Spike DNA was detected in the full genomic shotgun library of vaccine-treated samples with 3000x coverage. (Coverage means the percentage of the total base pair or locus of the genome covered by sequencing.) Since the coverage in the human genome was 30 times, we can see that the DNA with a large number of copies of the genome was invading the cell. As a result, strangely, SNP (monobasic polymorphism) was detected in deep sequencing at the origin of the vaccine plasmid replication (F1 and SV40). This SNP does not exist in the vaccine. In other words, it seems that plasmids are mutating in cells. Also, the coverage of deep sequencing in the replication origin area is higher than average, and the number of copies observed is relatively high, which means that the DNA embedded in the cell may be duplicated and mutated. I mean. Originally, plasmids and SV40 DNA replication require specific enzymes not owned by human cells. Experiments such as the introduction of large amounts of microDNA fragments containing replication points into cells are not usually performed in molecular genetics. It is possible that unexpected DNA replication is occurring within the cell. A total of two genomic integrations were observed in the vaccinated cell line from the analysis of Deep Sequencing by Dr. McKernan. Individual arrays of deep sequencing are called γ€Œ leads 」. It was very interesting data, so I tried to re-parse the lead myself. image Figure 2 Figure 2 is a lead showing genomic integration in Dr. McKernan's Deep Sequencing Analysis. The subject of the analysis is Genome Integration Leads 1 and 2. You can also read a lot of information from short array data. This time in comparison with the human genomeblat searchTo find homologyblast searchI used it. Now, after that, it will be my own re-parse. image Figure 3 The top of the array in Figure 3 is the lead. As you can tell by aligning this lead with the 12th chromosome (black) and the spike gene (red) of the Pfizer Corona vaccine, the 12th chromosome (black) is on the way to the spike gene (red). I am switching. And there is a short identical array (here GAGAG) in the place of switching. You can see that the end-recombination (MMEJ, Microhomology-mediated end joining) mediated by microhomology (microhomology) recombinates the contaminated DNA and human genome. Since MMEJ involves multiple intracellular DNA repair enzymes, this recombination is an artifact (mistake product) in the test tube. Instead, gene recombination may have occurred in cells. Genome integration occurs on the long arm of chromosome 12, and the FAIM2 gene is present at this locus. FAIM2 is a gene that has been suggested to be associated with cancer malignancy. Recombinations occur on introns (arrays that do not encode proteins), but I do not know how such mutations also affect gene expression. image Figure 4 Another example of genomic integration is Figure 4. If you align this lead with chromosome 9 (black) and spike gene (red), you can see that in the lead, chromosome 9 (black) is switching to the spike gene (red) on the way. There is a short identical array (here TCTGCCCT) in the place where this example also switches. After all, it is believed that the contaminated DNA and the human genome were recombined using microhomology. Since there are multiple pathways for DNA repair, which repair pathway is used when foreign DNA is taken into the genome is case-by-case. Part of the lead had an Illumina adapter array left. Adapter arrays are arrays granted to PCR amplify and sequence DNA for deep sequencing. Originally, the adapter array is removed during parsing, but often the removal is inadequate and remains in the lead. Integration of contaminated DNA into the genome is occurring near Centromea. Let's talk a little about Centromea. Two chromosomes with the same genetic information that can be done after DNA replication are chromatids (sister chromatids). The chromatids are connected until the chromosomes are distributed during cell division, but the region on the connected DNA is Centromea. As such, Centromea is an important area for chromosome separation and distribution. image Figure 5 Figure 5 is about the DNA fragments of the spike gene integrated into the genome. On the Pfizer Corona vaccine spike gene, the sequence found in the genome integrated lead was written in red. Due to lead length limitations, the actual integrated array will be even larger. The integrated sequence is part of the spike gene, and it is not possible to make a full-length spike sequence. However, it is unpredictable how contaminated DNA will be inserted into any area of the genome and have any effect. image Figure 6 Nucleotype (cario type) means the size, shape, and number of chromosomes. Human chromosomes consist of a total of 46 22 pairs of autosomal and one pair of sex chromosomes. The autosomal is assigned the number 1 chromosome, number 2 chromosome,, number 22 chromosome and number in order of size. The integrated site of contaminated DNA is the FAIM2 locus on the long arm of chromosome 9 and near Centromea on chromosome 12. The genomic integration observed this time is the first two cases in cultured cell experiments, but the specific identification of recombinant sequences with the human genome of contaminated DNA is a major advance. Further verification experiments will be advanced in the future. Genome integration, as in Figure 6, does not know which locus actually occurs on the genome. This is exactly the γ€Œ shotgun attack on the genome 」. What happens in cultured cells can also occur in normal cells, with a wide variety of alterations depending on the site of genomic integration. The first predicted catabolism is cancer induction and malignancy. And then, the ones that manifest themselves over time are various genetic diseases. What is known as a factor that causes genomic damage is, for example, radiation exposure, but genomic modification by contaminated DNA is different in that it is due to fragments of artificially created genes, and random mutations which are akin to radiation. But it is fundamentally different in nature. This experiment in cultured cells epitomizes genomic integration of contaminated DNA. This is a real problem that a large number of humans around the world, under the name of vaccination, are now experiencing aγ€Œ transfection human body experiment 」of contaminated DNA. The genomic modification of humanity is a direct consequence of the largest experiment in history of mRNA drug substance harm, and in the future it may be etched in history as theγ€Œ original sin 」of humanity. Original Social Engineering Sin Original Social Engineering Sin “...the socio-psychological foundations of socialism is identical to that of the foundations of a state, if there were no institution enforcing socialistic ideas of property, there would be no room for a state, as a state is nothing else than an institution built on taxation and unsolicited, noncontractual interference with the use that private people c… Read full story They want you dead. Do NOT comply. Upgrade to paid Shop 2SG merch Use code 2SGPET for 10% off PetMectin Use code 2SGPET for 10% off PetDazole Use code 2SGPET for 10% off FishCycline BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome 🧬 https://www.2ndsmartestguyintheworld.com/p/breaking-integration-of-corona-vaccine https://telegra.ph/BREAKING-Integration-of-corona-vaccine-contaminated-DNA-into-the-human-cell-line-genome-03-11
    WWW.2NDSMARTESTGUYINTHEWORLD.COM
    BREAKING: Integration of corona vaccine-contaminated DNA into the human cell line genome
    This important article further establishes that the Modified mRNA “vaccines” integrate into the cells. While these contaminated cells do not express the entire spike protein, but, rather, only part of it, the net effect is that the DNA of the “vaccinated” is irrevocably altered.
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  • The COVID-19 Vaccine Antigen Is ANTHRAX
    Dr. Ariyana Love
    By Dr. Ariyana Love

    Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein.

    We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX?

    “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

    Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention.

    A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

    According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

    Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

    The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out.


    Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides


    In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”.

    Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible.

    Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects.


    PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses


    The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

    In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg.

    Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs.

    Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant.

    The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels.

    Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

    Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

    SPIKE PROTEIN IS AEROSOLIZED ANTHRAX

    There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

    The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”.

    “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

    The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions.

    The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells.

    The following quote about the Anthrax “protective antigen” is particularly revealing:

    “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

    Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”.

    Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

    This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

    This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

    ALHYDROGEL

    According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel.

    Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

    In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

    In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

    Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network.

    Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

    This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from?

    This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

    “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

    Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public.

    Alhydrogel was improved and transformed into the Nanoalum adjuvant.

    Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

    Alhydrogel is also carried in the lipid coating of nanoparticles.

    The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.


    Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!


    ANTHRAX SYMPTOMS AND TREATMENT

    Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs.

    Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance).

    Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time.


    Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review


    Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers.

    The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis?

    Anthrax also coagulates the blood.

    “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

    Read more here and here.

    Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax.

    It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation.


    This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia.

    All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal.

    Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen.

    Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

    Heroine users in Europe have been tested with Injection Anthrax.

    Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind:

    “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

    TREATMENT

    If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax.

    Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

    Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol.

    I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system.

    Please follow me on Telegram @drloveariyana and X @drloveariyana.

    If you would like to donate to my research, please do so here.


    UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE.

    The Covid-19 Vaccine Antigen Is ANTHRAX

    Read more:
    https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true


    https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
    The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html
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  • The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders
    Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.

    The Epoch Times

    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    By Dr. Yuhong Dong

    Editor’s Note: This second installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here.

    Summary of key facts

    A Danish review of 79,102 female and 16,568 male subjects, found human papillomavirus (HPV) vaccines had significantly increased rates of serious nervous system disorders. Postural orthostatic tachycardia syndrome (POTS) and complex regional pain syndrome were judged “definitely associated” with the HPV vaccine.
    A large Danish and Swedish study including nearly 300,000 girls found a significant association between the HPV vaccine and increased rates of Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29).
    A large study including 3 million Danish and Swedish women aged 18 to 44, identified seven adverse events with statistically significant increased risks following HPV vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis, or encephalomyelitis.
    A 2017 French study of over 2.2 million young girls found evidence of a 3.78-fold increased risk of Guillain-Barré syndrome (GBS). A 2011 U.S. study found nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks post-Gardasil vaccination.
    While the underlying mechanisms causing these autoimmune reactions are not yet fully understood, some researchers speculate that the sizable overlap in protein sequences between the HPV and the human genome may cause the immune system to attack itself. Others are concerned that the adjuvants (such as aluminum) used to attract the attention of the immune system may be causing harm.
    Neurological and autoimmune disorders

    Danish review found increased nervous system disorder

    In 2020, a group of Danish scientists conducted a systematic review of the overall benefits and harms of HPV vaccines.

    Twenty-four eligible randomized controlled clinical studies were obtained, with a total of 95,670 participants, mostly women, and 49 months mean weighted follow-up.

    Almost all controls were given an active comparator vaccine (typically a hepatitis vaccine with a comparable aluminum-based adjuvant).

    Given that the adjuvant is highly immunogenic by design (it is meant to grab the attention of the immune system), this trial design makes it difficult to detect an excess risk with the HPV vaccines.

    Without true controls (such as a saline placebo), the real risks of HPV vaccination cannot be accurately assessed.

    In the vaccine group, 367 cancers were detected, compared to 490 in the comparator group.

    Younger participants (15 to 29) seemed to benefit more from the vaccine concerning preventing moderate HPV-related intraepithelial neoplasia compared to older participants (ages 21 to 72). Younger participants also had fewer fatal harms.

    Even though the studies were flawed in their design, at four years post-vaccination, those who had received the HPV vaccines had significantly increased rates of serious nervous system disorders: 49%, as well as general harms totaling 7%.

    The serious harms that were judged “definitely associated” with HPV vaccines were postural orthostatic tachycardia syndrome and complex regional pain syndrome. POTS had a nearly twofold increase in the vaccinated group.

    By July 2017, only two-thirds of the results from HPV vaccine trials had been published, and only about half the results had been posted, due to manuscript length limitations, reporting bias and confounding journal articles offering a limited view of trial outcomes.

    This Danish systematic review compiled data from all the HPV trials to offer a summary of the evidence thus far.

    Nevertheless, the investigators acknowledged that despite three years of work, the limitations of their analysis remained. These included reporting bias, incomplete reporting, data fragmentation and limited trial follow-up.

    These investigators similarly note that the trials were powered to assess the benefits of HPV vaccination, not rare harms. The degree to which benefits outweigh risks is therefore unknown.

    They concluded that future research should carefully evaluate the harms following Gardasil 9 compared to Gardasil because the former contains more than double the virus proteins and aluminum-containing adjuvant than the same dose of Gardasil.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

    Order Now

    Large studies reveal autoimmune events

    In 2009, the HPV4 vaccine was integrated into the Danish childhood vaccination program. Since then, two large cohort studies on the HPV4 vaccine adverse events have been carried out using the hospital-based healthcare registries of Denmark and Sweden.

    The first study in Denmark and Sweden included 296,826 girls aged 10 to 17 who received a total of 696,420 HPV4 vaccine doses.

    The scientists evaluated rate ratios for autoimmune events and found no significant association for 20 out of 23 events.

    They found a significant association between the HPV4 vaccine and Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29).

    But after further review, they concluded that there was insufficient evidence for a causal association, because of the weakness of the signal and the lack of an underlying mechanism to explain biological plausibility.

    In a second large cohort study, the same team expanded their research to more than 3 million Danish and Swedish adult women aged 18 to 44.

    The authors identified seven adverse events with statistically significant increased risks following HPV4 vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis or encephalomyelitis.

    After sensitivity analyses, the association between HPV4 vaccination and celiac disease was the most robust finding.

    Celiac disease is a condition where a person’s immune system attacks the body’s own gut after eating gluten.

    As the graph below shows, the scientists used two risk periods after HPV4 vaccination: the first 180 days and after.

    1 time since first dose HPV4 vaccine coeliac cases
    Time since the first dose of the HPV4 vaccine for vaccinated coeliac cases in a cohort of Danish and Swedish women. Credit: Journal of Internal Medicine
    The authors noted that the observed 56% increased risk of celiac disease “was strong, and the increase was strikingly similar in both risk periods after vaccination.”

    Celiac disease is underdiagnosed in Denmark.

    So one possible explanation is that vaccination visits allow a chance for this and other conditions to be diagnosed and explored.

    This explanation suggests that the association between the HPV vaccine and autoimmune disorders may be coincidental.

    However, given the lack of any real control groups in these studies, as well as the growing body of scientific literature from countries around the world showing problems with the HPV vaccine, dismissing these safety signals as coincidence seems short-sighted.

    Large French study and U.S. VAERS study identify risks of Guillain-Barré Syndrome

    The concern about autoimmune disease adverse events has contributed to low HPV vaccination uptake in France.

    A 2017 study of over 2.2 million young girls in France found troubling evidence of a link with Guillain-Barré syndrome. GBS is a condition that arises when our own antibodies attack the nerves.

    The incidence of GBS was found to be 1.4 per 100,000 person-years among the vaccinated girls compared to 0.4 per 100,000 among the unvaccinated, resulting in an increased risk of GBS of more than 200%.

    The association appeared to be “particularly marked in the first months following vaccination.”

    This finding is corroborated by the pattern of adverse reactions reported worldwide. Data from a large number of case reports document similar serious adverse events associated with Gardasil administration, with nervous system disorders of autoimmune origin being the most frequently reported.

    A 2011 U.S. study found that the estimated weekly reporting rate of post-Gardasil GBS within the first six weeks (6.6 per 10,000,000) was higher than in the general population, and higher than post-Menactra and post-influenza vaccinations.

    In particular, there was nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks after vaccination, compared to the general population.

    Additionally, the study found Gardasil vaccination was associated with approximately eight-and-a-half times more emergency department visits, 12.5 times more hospitalizations, 10 times more life-threatening events and 26.5 times more disability than the Menactra vaccination.

    Plausible mechanisms of harm

    Despite the conflicting data in the scientific literature to date, it is clear that the HPV vaccines can cause autoimmune disorders in susceptible people. But how?

    Autoimmunity has been reported as a complication of natural infection as well as virus vaccination. This phenomenon has been observed with many viruses, including the Epstein-Barr virus, COVID-19 and HPV.

    According to a 2019 study, the HPV vaccine contains epitopes — portions of the virus proteins — that overlap with the human proteins.

    This means that if we develop antibodies to those viruses, we may also generate autoantibodies to our own cells, which is the root cause of autoimmune dysfunction.

    The study showed that most of the immunoreactive HPV L1 epi­topes are overlapping peptides present in human proteins.

    The authors explained that this “unexpected enormous size of the peptide overlap between the HPV epitopes and human proteins” is relevant, and may be why a wide variety of autoimmune diseases have been reported post-HPV vaccination, including ovarian failure, systemic lupus erythematosus, breast cancer and sudden death, among others.

    Why some people develop these conditions and others do not is unclear.

    The authors suggest that vaccines should target the few peptides that do not overlap with human proteins, but which do overlap with the other HPVs.

    Despite this overlap and the potential for causing autoimmune disease, medical doctors usually ignore or dismiss the connection. We are told that these diseases are rare.

    The human body has something called immune tolerance. This protects a person’s immune system against attacking itself. Therefore, HPV infection is also “immune tolerated,” which means it lays dormant for some time until it becomes cancerous.

    HPV vaccination was actually designed with this immune tolerance in mind.

    Given the human body’s built-in defenses against autoimmune conditions, vaccinology requires an immunogenic catalyst to get the body’s attention. This is the job of an adjuvant.

    An adjuvant is an ingredient used in a vaccine that the body recognizes as foreign. It is added to vaccines so that the body will mount a stronger immune response.

    The idea is that in attacking the adjuvant, the body will also recognize other vaccine ingredients (in this case, purified HPV proteins).

    In addition, the antigen dose is much higher than in natural infections and the capsids in the vaccine are directly exposed to systemic immune responses as opposed to the virus staying relatively hidden within the natural barrier of the skin following infection.

    The vaccine was well-designed to trigger an immune response, but this advantage may come at a cost: Generating antibodies to HPV proteins through vaccination could, theoretically, set the stage for an autoimmune attack.

    Link between HPV-vaccine-associated nervous system dysfunction and autoimmunity

    A December 2022 Danish and German study was designed to elucidate a possible mechanism of harm.

    The lead author, Dr. Jesper Mehlsen, a specialist in treating autoimmune conditions, noted that the HPV major capsid L1s antigen resembles human autonomic nerve receptors, including G-protein coupled receptors (GPCR).

    According to the researchers, in the past several years, case series of suspected vaccination side effects have pointed to three disease entities: POTS, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and complex regional pain syndrome. These syndromes may be associated with neuroendocrine GPCR antibodies.

    From 2011 to 2018, researchers saw 845 patients (839 females, six males) with suspected side effects following the HPV4 vaccine. The control group included vaccinated people without side effects.

    Moderate to severe fatigue was recorded in 83.3% of the patients but in none of the controls.

    A high prevalence of symptoms, such as dizziness (91%), heart palpitations (71%), nausea (80%) and hyperactive bladder suggested that the patients were experiencing some kind of autonomic dysfunction.

    Autonomic dysfunction occurs when the part of the nervous system that controls well-being and balance does not function properly.

    2 most frequent symptoms hpv vaccine
    Most frequent symptoms reported by 612 patients in Denmark. Credit: Journal of Autoimmunity
    Twenty-four percent higher antinuclear antibodies (ANA, a common type of autoantibodies) were found in patients, suggesting possible autoimmunity.

    3 antinuclear antibodies HPV vaccines
    A larger proportion of the symptomatic patients were found with a common type of autoantibodies compared to healthy controls. Credit: Journal of Autoimmunity
    Antibodies against the adrenergic ß-2-receptor and muscarinic M-2 receptors were also found significantly higher in patients.

    Many of the symptoms, including immune activation and autonomic dysregulation, could be mediated or aggravated by dysregulated autoantibodies against adrenergic receptors and impaired peripheral adrenergic function.

    The authors suggested that girls and women with probable side effects of HPV vaccination have symptoms and biological markers compatible with an autoimmune disease closely resembling that seen in ME/CFS.

    Interestingly, people who already had HPV infections at some point appeared to be at greater risk for adverse events following vaccination.

    The authors noted that “prior disease may precondition some individuals for vaccine-related adverse events.”

    They also noted that some of the adverse events resembled long-COVID symptoms.

    Universal HPV vaccination called into question

    Academic researcher at the University of British Columbia, Lucija Tomljenovic, and neuroscientist Christopher Shaw, who have closely looked into Gardasil, have argued that the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.

    In a 2012 comment published in the American Journal of Public Health, they took issue with “incomplete and inaccurate” data and poorly designed trials.

    Vaccination is unjustified if the vaccine carries any substantial risk, as healthy teenagers face little to no risk of dying from cervical cancer.

    Risk-benefit analyses must be conducted to ascertain the overall balance of benefits and harms on both individual and societal levels.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland.

    If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari.

    The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense.

    https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-2-et/

    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-2.html
    The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Dr. Yuhong Dong Editor’s Note: This second installment in a multi-part series about the human papillomavirus, or HPV, vaccine examines studies that link the vaccines to increased risk of serious neurological and autoimmune disorders. Read Part 1 here. Summary of key facts A Danish review of 79,102 female and 16,568 male subjects, found human papillomavirus (HPV) vaccines had significantly increased rates of serious nervous system disorders. Postural orthostatic tachycardia syndrome (POTS) and complex regional pain syndrome were judged “definitely associated” with the HPV vaccine. A large Danish and Swedish study including nearly 300,000 girls found a significant association between the HPV vaccine and increased rates of Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29). A large study including 3 million Danish and Swedish women aged 18 to 44, identified seven adverse events with statistically significant increased risks following HPV vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis, or encephalomyelitis. A 2017 French study of over 2.2 million young girls found evidence of a 3.78-fold increased risk of Guillain-Barré syndrome (GBS). A 2011 U.S. study found nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks post-Gardasil vaccination. While the underlying mechanisms causing these autoimmune reactions are not yet fully understood, some researchers speculate that the sizable overlap in protein sequences between the HPV and the human genome may cause the immune system to attack itself. Others are concerned that the adjuvants (such as aluminum) used to attract the attention of the immune system may be causing harm. Neurological and autoimmune disorders Danish review found increased nervous system disorder In 2020, a group of Danish scientists conducted a systematic review of the overall benefits and harms of HPV vaccines. Twenty-four eligible randomized controlled clinical studies were obtained, with a total of 95,670 participants, mostly women, and 49 months mean weighted follow-up. Almost all controls were given an active comparator vaccine (typically a hepatitis vaccine with a comparable aluminum-based adjuvant). Given that the adjuvant is highly immunogenic by design (it is meant to grab the attention of the immune system), this trial design makes it difficult to detect an excess risk with the HPV vaccines. Without true controls (such as a saline placebo), the real risks of HPV vaccination cannot be accurately assessed. In the vaccine group, 367 cancers were detected, compared to 490 in the comparator group. Younger participants (15 to 29) seemed to benefit more from the vaccine concerning preventing moderate HPV-related intraepithelial neoplasia compared to older participants (ages 21 to 72). Younger participants also had fewer fatal harms. Even though the studies were flawed in their design, at four years post-vaccination, those who had received the HPV vaccines had significantly increased rates of serious nervous system disorders: 49%, as well as general harms totaling 7%. The serious harms that were judged “definitely associated” with HPV vaccines were postural orthostatic tachycardia syndrome and complex regional pain syndrome. POTS had a nearly twofold increase in the vaccinated group. By July 2017, only two-thirds of the results from HPV vaccine trials had been published, and only about half the results had been posted, due to manuscript length limitations, reporting bias and confounding journal articles offering a limited view of trial outcomes. This Danish systematic review compiled data from all the HPV trials to offer a summary of the evidence thus far. Nevertheless, the investigators acknowledged that despite three years of work, the limitations of their analysis remained. These included reporting bias, incomplete reporting, data fragmentation and limited trial follow-up. These investigators similarly note that the trials were powered to assess the benefits of HPV vaccination, not rare harms. The degree to which benefits outweigh risks is therefore unknown. They concluded that future research should carefully evaluate the harms following Gardasil 9 compared to Gardasil because the former contains more than double the virus proteins and aluminum-containing adjuvant than the same dose of Gardasil. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now Large studies reveal autoimmune events In 2009, the HPV4 vaccine was integrated into the Danish childhood vaccination program. Since then, two large cohort studies on the HPV4 vaccine adverse events have been carried out using the hospital-based healthcare registries of Denmark and Sweden. The first study in Denmark and Sweden included 296,826 girls aged 10 to 17 who received a total of 696,420 HPV4 vaccine doses. The scientists evaluated rate ratios for autoimmune events and found no significant association for 20 out of 23 events. They found a significant association between the HPV4 vaccine and Bechet’s syndrome (rate ratio 3.37), Raynaud’s disease (1.67) and type 1 diabetes (1.29). But after further review, they concluded that there was insufficient evidence for a causal association, because of the weakness of the signal and the lack of an underlying mechanism to explain biological plausibility. In a second large cohort study, the same team expanded their research to more than 3 million Danish and Swedish adult women aged 18 to 44. The authors identified seven adverse events with statistically significant increased risks following HPV4 vaccination: Hashimoto’s thyroiditis, celiac disease, lupus erythematosus, pemphigus vulgaris, Addison’s disease, Raynaud’s disease and encephalitis, myelitis or encephalomyelitis. After sensitivity analyses, the association between HPV4 vaccination and celiac disease was the most robust finding. Celiac disease is a condition where a person’s immune system attacks the body’s own gut after eating gluten. As the graph below shows, the scientists used two risk periods after HPV4 vaccination: the first 180 days and after. 1 time since first dose HPV4 vaccine coeliac cases Time since the first dose of the HPV4 vaccine for vaccinated coeliac cases in a cohort of Danish and Swedish women. Credit: Journal of Internal Medicine The authors noted that the observed 56% increased risk of celiac disease “was strong, and the increase was strikingly similar in both risk periods after vaccination.” Celiac disease is underdiagnosed in Denmark. So one possible explanation is that vaccination visits allow a chance for this and other conditions to be diagnosed and explored. This explanation suggests that the association between the HPV vaccine and autoimmune disorders may be coincidental. However, given the lack of any real control groups in these studies, as well as the growing body of scientific literature from countries around the world showing problems with the HPV vaccine, dismissing these safety signals as coincidence seems short-sighted. Large French study and U.S. VAERS study identify risks of Guillain-Barré Syndrome The concern about autoimmune disease adverse events has contributed to low HPV vaccination uptake in France. A 2017 study of over 2.2 million young girls in France found troubling evidence of a link with Guillain-Barré syndrome. GBS is a condition that arises when our own antibodies attack the nerves. The incidence of GBS was found to be 1.4 per 100,000 person-years among the vaccinated girls compared to 0.4 per 100,000 among the unvaccinated, resulting in an increased risk of GBS of more than 200%. The association appeared to be “particularly marked in the first months following vaccination.” This finding is corroborated by the pattern of adverse reactions reported worldwide. Data from a large number of case reports document similar serious adverse events associated with Gardasil administration, with nervous system disorders of autoimmune origin being the most frequently reported. A 2011 U.S. study found that the estimated weekly reporting rate of post-Gardasil GBS within the first six weeks (6.6 per 10,000,000) was higher than in the general population, and higher than post-Menactra and post-influenza vaccinations. In particular, there was nearly a two-and-a-half to 10 times greater risk of acquiring GBS within six weeks after vaccination, compared to the general population. Additionally, the study found Gardasil vaccination was associated with approximately eight-and-a-half times more emergency department visits, 12.5 times more hospitalizations, 10 times more life-threatening events and 26.5 times more disability than the Menactra vaccination. Plausible mechanisms of harm Despite the conflicting data in the scientific literature to date, it is clear that the HPV vaccines can cause autoimmune disorders in susceptible people. But how? Autoimmunity has been reported as a complication of natural infection as well as virus vaccination. This phenomenon has been observed with many viruses, including the Epstein-Barr virus, COVID-19 and HPV. According to a 2019 study, the HPV vaccine contains epitopes — portions of the virus proteins — that overlap with the human proteins. This means that if we develop antibodies to those viruses, we may also generate autoantibodies to our own cells, which is the root cause of autoimmune dysfunction. The study showed that most of the immunoreactive HPV L1 epi­topes are overlapping peptides present in human proteins. The authors explained that this “unexpected enormous size of the peptide overlap between the HPV epitopes and human proteins” is relevant, and may be why a wide variety of autoimmune diseases have been reported post-HPV vaccination, including ovarian failure, systemic lupus erythematosus, breast cancer and sudden death, among others. Why some people develop these conditions and others do not is unclear. The authors suggest that vaccines should target the few peptides that do not overlap with human proteins, but which do overlap with the other HPVs. Despite this overlap and the potential for causing autoimmune disease, medical doctors usually ignore or dismiss the connection. We are told that these diseases are rare. The human body has something called immune tolerance. This protects a person’s immune system against attacking itself. Therefore, HPV infection is also “immune tolerated,” which means it lays dormant for some time until it becomes cancerous. HPV vaccination was actually designed with this immune tolerance in mind. Given the human body’s built-in defenses against autoimmune conditions, vaccinology requires an immunogenic catalyst to get the body’s attention. This is the job of an adjuvant. An adjuvant is an ingredient used in a vaccine that the body recognizes as foreign. It is added to vaccines so that the body will mount a stronger immune response. The idea is that in attacking the adjuvant, the body will also recognize other vaccine ingredients (in this case, purified HPV proteins). In addition, the antigen dose is much higher than in natural infections and the capsids in the vaccine are directly exposed to systemic immune responses as opposed to the virus staying relatively hidden within the natural barrier of the skin following infection. The vaccine was well-designed to trigger an immune response, but this advantage may come at a cost: Generating antibodies to HPV proteins through vaccination could, theoretically, set the stage for an autoimmune attack. Link between HPV-vaccine-associated nervous system dysfunction and autoimmunity A December 2022 Danish and German study was designed to elucidate a possible mechanism of harm. The lead author, Dr. Jesper Mehlsen, a specialist in treating autoimmune conditions, noted that the HPV major capsid L1s antigen resembles human autonomic nerve receptors, including G-protein coupled receptors (GPCR). According to the researchers, in the past several years, case series of suspected vaccination side effects have pointed to three disease entities: POTS, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and complex regional pain syndrome. These syndromes may be associated with neuroendocrine GPCR antibodies. From 2011 to 2018, researchers saw 845 patients (839 females, six males) with suspected side effects following the HPV4 vaccine. The control group included vaccinated people without side effects. Moderate to severe fatigue was recorded in 83.3% of the patients but in none of the controls. A high prevalence of symptoms, such as dizziness (91%), heart palpitations (71%), nausea (80%) and hyperactive bladder suggested that the patients were experiencing some kind of autonomic dysfunction. Autonomic dysfunction occurs when the part of the nervous system that controls well-being and balance does not function properly. 2 most frequent symptoms hpv vaccine Most frequent symptoms reported by 612 patients in Denmark. Credit: Journal of Autoimmunity Twenty-four percent higher antinuclear antibodies (ANA, a common type of autoantibodies) were found in patients, suggesting possible autoimmunity. 3 antinuclear antibodies HPV vaccines A larger proportion of the symptomatic patients were found with a common type of autoantibodies compared to healthy controls. Credit: Journal of Autoimmunity Antibodies against the adrenergic ß-2-receptor and muscarinic M-2 receptors were also found significantly higher in patients. Many of the symptoms, including immune activation and autonomic dysregulation, could be mediated or aggravated by dysregulated autoantibodies against adrenergic receptors and impaired peripheral adrenergic function. The authors suggested that girls and women with probable side effects of HPV vaccination have symptoms and biological markers compatible with an autoimmune disease closely resembling that seen in ME/CFS. Interestingly, people who already had HPV infections at some point appeared to be at greater risk for adverse events following vaccination. The authors noted that “prior disease may precondition some individuals for vaccine-related adverse events.” They also noted that some of the adverse events resembled long-COVID symptoms. Universal HPV vaccination called into question Academic researcher at the University of British Columbia, Lucija Tomljenovic, and neuroscientist Christopher Shaw, who have closely looked into Gardasil, have argued that the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits. In a 2012 comment published in the American Journal of Public Health, they took issue with “incomplete and inaccurate” data and poorly designed trials. Vaccination is unjustified if the vaccine carries any substantial risk, as healthy teenagers face little to no risk of dying from cervical cancer. Risk-benefit analyses must be conducted to ascertain the overall balance of benefits and harms on both individual and societal levels. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases in China, is the chief scientific officer and co-founder of a Swiss biotech company and former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense. https://childrenshealthdefense.org/defender/truth-hpv-vaccine-part-2-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-2.html
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    The Truth About HPV Vaccination, Part 2: Studies Link the Vaccines to Neurological, Autoimmune Disorders
    Researchers who looked closely into the Gardasil HPV vaccine concluded the risks from the vaccine seem to significantly outweigh the as-yet-unproven long-term benefits.
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  • The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.

    The Epoch Times

    Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free.

    By Yuhong Dong

    The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date.

    Summary of Key Facts

    This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006.
    In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward.
    International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1.
    The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury.

    In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm.

    The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries.

    More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence.

    Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome.

    While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus.

    RFK Jr. and Brian Hooker Vax-Unvax
    RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax”

    Order Now

    What is HPV?

    According to the CDC, HPV is the most common sexually transmitted infection in the U.S.

    HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified.

    HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms.

    HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses.

    HPV-associated cancers

    High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers.

    Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers.

    An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers.

    Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper.

    Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease.

    In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men.

    But in 9 out of 10 cases, HPV goes away within two years without causing health problems.

    Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses.

    The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests.

    HPV vaccines

    Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA.

    The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious.

    Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.”

    Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18).

    On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers.

    According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection.

    On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer.

    In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26.

    Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers.

    Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58).

    The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first.

    For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient.

    The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection.

    The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active.

    HPV VAERS reports from 2 large countries

    U.S. HPV vaccine adverse events

    On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008.

    During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious.

    VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups.

    Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines.

    A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively.

    The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders.

    Australia HPV vaccines adverse events

    In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006.

    Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine.

    1 vaccine adverse events australia chart
    In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care.
    Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.”

    2 vaccine types vaccine suspected chart
    In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care.
    Japan withdraws recommendation, vaccine acceptance plunged

    In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%.

    Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.”

    The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.”

    In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths.

    However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued?

    Ovarian insufficiency

    Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature.

    In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine.

    This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.”

    VAERS analysis on ovarian failure

    Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations.

    The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination.

    The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%).

    Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46.

    The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns.

    For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk.

    But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination.

    In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”).

    Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link.

    The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.”

    However, the benefit-risk profile on an individual level is not uniform.

    Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear.

    3 case reports on ovarian insufficiency

    In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination.

    As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency.

    One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency.

    Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause.

    She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal.

    The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system.

    However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating.

    The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms.

    Danish retrospective cohort study finds no link

    A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years.

    The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96.

    One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course.

    The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency.

    Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland.

    If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari.

    The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense.

    https://childrenshealthdefense.org/defender/hpv-vaccine-safety-concerns-part-1-et/


    https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html
    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really? This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe. The Epoch Times Miss a day, miss a lot. Subscribe to The Defender's Top News of the Day. It's free. By Yuhong Dong The decline of public trust in COVID-19 vaccines significantly impacts vaccination rates against routine childhood diseases. This multiple-part series explores the international research done over the past two decades on the human papillomavirus (HPV) vaccine — believed to be one of the most effective vaccines developed to date. Summary of Key Facts This multiple-part series offers a thorough analysis of concerns raised about HPV vaccination following the global HPV campaign, which commenced in 2006. In the U.S., the HPV vaccine was reported to have a disproportionately higher percentage of adverse events of fainting and blood clots in the veins. The U.S. Food and Drug Administration (FDA) acknowledges that fainting can happen following the HPV vaccine, and recommends sitting or lying down to get the shot, then waiting for 15 minutes afterward. International scientists found that the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) logged a substantial increase in reports of premature ovarian failure from 1.4 per year before 2006 to 22.2 per year after the HPV vaccine approval, yielding a Proportional Reporting Ratio of 46.1. The HPV vaccine is widely regarded as one of the most effective vaccines developed to date. Nevertheless, safety issues have been raised following its approval, and in response, additional research has been published and litigation has been brought on behalf of those with a vaccine injury. In this HPV vaccine series, Parts I and II explain how the vaccine works and the evidence suggesting there may be legitimate safety concerns. The remaining parts present questions about real-world vaccine effectiveness and identify specific ingredients which may pose harm. The information presented here is drawn from peer-reviewed scientific literature from the U.S., Australia, Denmark, Sweden, France and Japan, as well as statistics published by public health agencies in each of these countries. More than 100 hours of research and internal peer review among scientists with experience in infectious diseases, virology, clinical trials and vaccine epidemiology have been invested in presenting this summary of the evidence. Large registry-based studies have identified plausible associations between HPV vaccination and autoimmune conditions, including premature ovarian insufficiency or premature ovarian failure, Guillain-Barré syndrome (GBS), postural orthostatic tachycardia syndrome and chronic regional pain syndrome. While it is easy to be enthusiastic about recent advances in human vaccine technology, we should keep in mind that achieving real and lasting good health is much more than just the absence of a certain virus. RFK Jr. and Brian Hooker Vax-Unvax RFK Jr. and Brian Hooker’s New Book: “Vax-Unvax” Order Now What is HPV? According to the CDC, HPV is the most common sexually transmitted infection in the U.S. HPV is a small DNA virus infecting human cutaneous epithelial cells in the mucosa and skin. More than 150 strains of the HPV virus have been identified. HPV infection is so common that the majority of sexually active people will get it at some point in their lives, even if they have only one or very few sexual partners. It can spread through sexual intercourse and oral sex. It can also pass between people through skin-to-skin contact, even by people who have no symptoms. HPV infection causes genital warts, some of which can turn into cancer. For the most part, however, HPV infection is benign. More than 90% of HPV infections cause no clinical symptoms and are self-limited, meaning the virus is cleared by the body via natural immunological defenses. HPV-associated cancers High-risk HPV types (types 16, 18 and others) can cause cervical cell abnormalities that are precursors to cancers. Type 16 is associated with approximately 50% of cervical cancers worldwide, and types 16 and 18 together are linked to 66% of cervical cancers. An additional five high-risk types, 31, 33, 45, 52 and 58, are linked with another 15% of cervical cancers and 11% of all HPV-associated cancers. Infection with a high-risk HPV type is associated with a higher chance of the development of cervical cancer but, by itself, HPV infection is not the sole risk factor to cause cancer. There are many other reasons, as discussed in this paper. Given the prevalence of infection, it is unsurprising that globally, cervical cancer is the fourth most common cancer in women. In 2018, an estimated 570,000 women were diagnosed with cervical cancer worldwide and more than 300,000 died of the disease. In the U.S., nearly 50,000 new HPV-associated cancers occur annually, with women infected at a slightly higher rate than men. But in 9 out of 10 cases, HPV goes away within two years without causing health problems. Only persistent HPV infections may lead to cancer. These infections evade the immune system’s innate cell-mediated defenses. The incidence of cervical cancer can be controlled as a result of the implementation of routine testing and screening, including Pap and DNA tests. HPV vaccines Three HPV vaccines — bivalent HPV vaccine (Cervarix, 2vHPV), quadrivalent HPV vaccine (Gardasil, 4vHPV or HPV4) and 9-valent HPV vaccine (Gardasil 9, 9vHPV) — have been licensed by the FDA. The HPV vaccine uses recombinant technology to assemble the shell of the virus — L1 capsid protein. These viral-like particles do not contain the virus genome and are not infectious. Cervarix, developed by GlaxoSmithKline, is a bivalent vaccine against HPV types 16 and 18, that was pulled from the U.S. market in 2016 due to “very low market demand.” Merck’s original Gardasil vaccine was designed to prevent infections from four strains (types 6, 11, 16 and 18). On June 8, 2006, after the FDA’s fast-tracked review, Gardasil was approved for use in females ages 9 to 26 for the prevention of cervical, vulvar and vaginal cancers. According to the label accompanying the vaccine, the ingredients in Merck’s first Gardasil vaccine were proteins of HPV, amorphous aluminum hydroxyphosphate sulfate, yeast protein, sodium chloride, L-histidine, polysorbate 80, sodium borate and water for injection. On Oct. 16, 2009, the FDA approved Gardasil (HPV4) for use in boys ages 9 through 26 for the prevention of genital warts caused by HPV types 6 and 11, but not for cancer. In 2010, it approved Gardasil for the prevention of anal cancer in males and females ages 9 to 26. Four years later, the FDA approved an updated vaccine, Merck’s Gardasil 9, for use in girls ages 9 to 26 and boys ages 9 to 15 for the prevention of cervical, vaginal and anal cancers. Gardasil 9 contains the same ingredients as Gardasil, but offers protection against nine HPV strains, adding five additional types (HPV types 31, 33, 45, 52 and 58). The current HPV vaccination schedule recommended by the CDC is two doses for both boys and girls aged 11 or 12. However, it is approved for children as young as 9. The second dose is given 6 to 12 months after the first. For those aged 15 and above, a three-dose schedule is implemented at one- to two-month and six-month intervals, although antibody-level studies suggest that two doses are sufficient. The vaccine prompts the body to produce neutralizing antibodies against HPV. Antibody responses appear to peak seven months after the first dose (or one month after the third dose). The vaccine-induced antibody levels appear to be 10 to 100 times higher than those after natural infection. The high vaccine effectiveness (90 to 98%) against the fast-growing, abnormal cells which may cause precancerous lesions in people ages 16 to 26 suggested that the best timing for vaccination was to give it to patients before they became sexually active. HPV VAERS reports from 2 large countries U.S. HPV vaccine adverse events On Aug. 19, 2009, the Journal of the American Medical Association published an article authored by scientists from the FDA and CDC that reviewed the safety data for Gardasil for adverse events reported to VAERS between June 2006 through December 2008. During that time, there were 12,424 reports of adverse events. Of these, 772 (6.2%) were serious. VAERS is a passive surveillance system, which is subject to multiple limitations, including underreporting, unconfirmed diagnosis, lack of denominator data and no unbiased comparison groups. Nevertheless, it is a useful and important tool for detecting postmarket safety issues with vaccines. A disproportionately high percentage of Gardasil VAERS reports were of syncope (fainting) and venous thromboembolic events (blood clots in the veins) compared with other vaccines. There were 8.2 syncope events per 100,000 HPV doses and 0.2 venous thromboembolic events per 100,000 HPV doses reported, respectively. The Gardasil package insert includes a warning about fainting, fever, dizziness, nausea and headaches (page 1) and notes at least the following adverse reactions reported during postmarketing surveillance (section 6.2): Guillain-Barré syndrome, transverse myelitis, motor neuron disease, venous thromboembolic events, pancreatitis and autoimmune disorders. Australia HPV vaccines adverse events In 2007, Australia reported an annual adverse drug reaction rate of 7.3/100,000, the highest since 2003, representing an 85% increase from 2006. Per the analysis of the Adverse Drug Reactions System database by the Australian Department of Health and Aging, this increase was “almost entirely due to” reports following the national rollout of the three-dose HPV vaccination program for young females in April 2007; 705 of the 1,538 adverse drug reactions reported that year were from the Gardasil vaccine. 1 vaccine adverse events australia chart In Australia, the ADR increase in 2007 was almost entirely due to the three-dose HPV vaccination program for females aged 12 to 26 years in April 2007. Credit: Australian Government Department of Health and Aged Care. Moreover, though people may take different vaccines other than HPV, the HPV vaccine was the only suspected vaccine to cause adverse reactions in 96% of records. Twenty-nine percent had causality ratings of “certain” or “probable” and 6% were defined as “serious.” 2 vaccine types vaccine suspected chart In these HPV-induced ADRs, 674 were suspected to be related to HPV vaccines, 203 had causality ratings of “certain” or “probable,” and 43 were defined as “serious.” Credit: Australian Government Department of Health and Aged Care. Japan withdraws recommendation, vaccine acceptance plunged In 2013, the Japanese raised concerns about a variety of widely reported post-vaccination serious adverse events. This led the government to suspend recommending the HPV vaccine for six years. Vaccine acceptance of HPV in Japan plunged significantly after 2013, from 42.9% to 14.3%, or from 65.4% to 3.9%. Researchers around the world also started to investigate HPV safety. A World Health Organization (WHO) position paper released on July 14, 2017, concluded that the HPV vaccines were “extremely safe.” The same report estimated approximately 1.7 cases of anaphylaxis per million HPV doses, that no association with GBS was found, and that syncope (fainting) was “established as a common anxiety or stress-related reaction to the injection.” In the spring of 2022, Japan announced it was relaunching its HPV vaccination drive. Mainstream news outlets reported that for thousands of women, the cost of caution may have led to preventable HPV-induced cancers and an estimated 5,000 to 5,700 deaths. However, a true risk-benefit analysis would also consider the number of serious adverse events prevented by putting the program on hold. The question remains: Was Japan’s caution warranted, or should their national vaccination program have continued? Ovarian insufficiency Concerns that the vaccine may be negatively affecting fertility have been detailed in the scientific literature. In 2014, a peer-reviewed case series describing premature ovarian failure among Australian women following HPV vaccination was published in the Journal of Investigative Medicine. This prompted other researchers to systematically examine the VAERS data to see if there was a connection between premature ovarian failure and Gardasil. Their study found a “potential safety signal” and concluded that “further investigations are warranted.” VAERS analysis on ovarian failure Two recent publications based on VAERS reports (first study, second study) found that events with a probable autoimmune background were significantly more frequent after HPV vaccination compared to other vaccinations. The team of international scientists that did the second study evaluated reports between 1990 and 2018. They found that among the 228,341 premature ovarian failure reports, 0.1% was considered to be associated with HPV vaccination with a median age of 15 years and the time to onset was 20.5 days following vaccination. The primary symptoms were amenorrhea (80.4%) and premature menopause (15.3%). Most strikingly, the mean number of premature ovarian failure cases increased significantly from 1.4 per year prior to 2006 to 22.2 per year after the HPV vaccine was approved, with a proportional reporting ratio of 46. The investigators noted that the WHO and CDC declared the HPV vaccine safe regardless of lacking adequate research into safety concerns. For example, the authors note that in a CDC-sponsored VAERS study, 17 cases of premature ovarian failure were identified but 15 were excluded due to insufficient information to confirm the diagnosis. A separate observational study using the Vaccine Safety Datalink found no increased risk. But this study was too underpowered to detect a signal. In addition, a cross-sectional survey study using National Health and Nutrition Examination Survey data relied on an inaccurate measurement of premature ovarian failure and self-reported HPV vaccination. In summary, the researchers detected a strong safety signal even after accounting for a potential upswing in reports due to media coverage after the product launch (they refer to this as “notoriety bias”). Because VAERS is a passive reporting system, the data may be incomplete and are often unconfirmed by physicians. Therefore, this study cannot provide a definitive link between HPV vaccination and premature ovarian insufficiency or premature ovarian failure but does generate a hypothetical link. The authors of the second study conclude by insisting that “this signal warrants well-designed and appropriate epidemiological research.” They note that “if the signal is confirmed, the risk is small compared to the lifetime risk of cervical cancer.” However, the benefit-risk profile on an individual level is not uniform. Given the health impacts of premature ovarian insufficiency and premature ovarian failure — some of which may be irreversible — and the declining mortality rate for cervical cancer even in the prevaccine era, the risk-benefit profile for HPV vaccination remains unclear. 3 case reports on ovarian insufficiency In the 2014 investigation mentioned above, a general practitioner in Australia noticed that three girls developed premature ovarian insufficiency following HPV4 vaccination. As a result of vaccination, each of the girls (ages 16, 16 and 18) had been prescribed oral contraception to treat menstrual cycle irregularities. Typically, women present with amenorrhea (no periods) or oligomenorrhea (infrequent periods) as the initial symptom of premature ovarian insufficiency. One girl had irregular periods following three doses of HPV vaccination. She then became amenorrheic and was diagnosed with premature ovarian insufficiency. Another girl’s periods were “like clockwork” until after the third HPV dose, which she received at age 15. Her first cycle after being vaccinated for the third time started two weeks late, and her next cycle was two months late. The final cycle began nine months later. The patient had no family history of early menopause. She was diagnosed with premature ovarian failure at 16. Lab work found hormone levels consistent with those of postmenopausal women, but her bone mineral density was normal. The authors of this case series noted that in preclinical studies of HPV4, the five-week-old rats only conceived one litter and the only available toxicology studies appear to be on the male rodent reproductive system. However, only two of three doses were administered prior to mating, and the overall fecundity was 95%, slightly lower than the control rats (98%) that received no vaccination prior to mating. The dose tolerance recommendations were based on an average weight of 50 kilograms for an adolescent girl but failed to take into account that HPV4 is administered to girls ages 9 to 13 years, who range in weight from 28 to 46 kilograms. Danish retrospective cohort study finds no link A 2021 study also evaluated premature ovarian insufficiency in a nationwide cohort of nearly 1 million Danish females ages 11 to 34 years. The researchers used Cox proportional hazard regression to detect an increased risk of premature ovarian insufficiency diagnosis by HPV4 vaccination status during the years 2007-2016. The hazard ratio for premature ovarian insufficiency (vaccinated versus unvaccinated) was 0.96. One limitation was that data on age at menarche (first menstruation) and oral contraceptive use were not available. Girls who had not yet reached menarche would not be at risk for premature ovarian insufficiency, of course. The authors excluded girls under age 15 in a sensitivity analysis and still found no signal, concluding that no association was found between HPV4 vaccination and premature ovarian insufficiency. Reprinted with permission from The Epoch Times. Dr. Yuhong Dong, a medical doctor who also holds a doctorate in infectious diseases from China, is the chief scientific officer and co-founder of a Swiss biotech company and a former senior medical scientific expert for antiviral drug development at Novartis Pharma in Switzerland. If you or your child suffered harm after receiving the Gardasil HPV vaccine, you may have a legal claim. Please visit Wisner Baum for a free case evaluation. Click here to watch a Gardasil litigation update interview with Wisner Baum Senior Partner Bijan Esfandiari. The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children's Health Defense. https://childrenshealthdefense.org/defender/hpv-vaccine-safety-concerns-part-1-et/ https://donshafi911.blogspot.com/2024/01/the-truth-about-hpv-vaccination-part-1.html
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    The Truth About HPV Vaccination, Part 1: How Safe Is It, Really?
    This first installment in a multi-part series about the human papillomavirus, or HPV, vaccine explores peer-reviewed scientific literature that reveals serious safety concerns about a vaccine widely regarded as safe.
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