Excerpt:

The World Council for Health on Monday convened an international panel of scientists and medical experts to discuss recent revelations that COVID-19 mRNA vaccines are contaminated with bacterial DNA plasmids that can harm human health.

Describing the findings as “probably the most important topic of our time,” the panelists addressed “#PlasmidGate” and its implications “for all people of the world.”

The hearing addressed the discovery of bacterial DNA left over from the microscopic plasmids used for multiplying DNA in the mRNA vaccine manufacturing process. One of the gene therapy tools discovered in COVID-19 vaccines is SV40, which is known to be cancer-promoting.

These foreign substances may also be responsible for the high numbers of severe adverse events and deaths following COVID-19 vaccines — but health regulators across the world have thus far ignored the connection, participants said.

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Bhakdi told The Defender, “We feel that the plasmid discovery could be the game-changer,” because genome alteration leads to the creation of genetically modified humans, which he said “will not be tolerated by the world.”

“Physicians around the globe face the decision whether they want to save themselves or go down in history as accomplices in the greatest crime against humanity. We believe that here lies a real chance,” Bkahdi said.

Data and testimony presented Monday centered around McKernan’s finding, replicated by other researchers, that up to 35% of the content of mRNA COVID-19 vaccines consists of DNA plasmids.

Plothe described plasmids as “a circular ring of DNA in which elements, via genetic modifications, have been put in, in order to produce the mRNAs.”

“[b]Logically, [plasmids] should not be in the vaccine, because they’re the production sites of mRNA and you certainly don’t want them to be lasting in your body[/b],” Plothe said, adding that such plasmids contribute to antibiotic resistance.

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The COVID vaccine ‘bait and switch’

McKernan noted that vials of COVID-19 vaccine used in clinical trials and later approved “are not the vials that were given to the public.”

The clinical trial administered a vaccine made with “process one,” which used PCR to make the DNA that was then turned into the RNA to make the spike protein, McKernan explained.

However, “Once the trial was complete, they [performed] a big bait and switch,” he said. “They moved to a production process that manufactured this DNA in E. coli.”

“With that comes a different risk,” McKernan said. “When they switched to scale this up, … now you had to get the DNA out of E. coli and not have any of the parts of E. coli come with it.”

McKernan explained that parts of E. coli are known endotoxins that can cause anaphylaxis, a severe allergic reaction.

Bhakdi said, “Contamination of mRNA vaccines with plasmid DNA … must be expected to be the rule and not the exception.”

SV40 DNA ‘the most striking revelation’

McKernan discussed “the most striking revelation”: SV40 cancer-promoting components found in the Pfizer monovalent vaccines. These were “not disclosed to the regulators,” he said.

This is important, McKernan said, because “SV40 is a well-published tool for gene therapy. If you want to get DNA into the nucleus, this is the shuttle that you use to get it done.”

According to McCullough, SV40 stands for Simian Virus 40. “These are known commercial enhancers to upregulate the production of a gene in E. coli to produce a product,” he said.

The SV40 genetic code is well-known to be taken up into human cells and to potentially cause cancer. “It promotes proto-oncogenes to turn on and actually become cancerous within cells,” McCullough said.

Lindsay called SV40 a “super promoter,” explaining that SV40 is “great at driving gene expression and if that should sit above an oncogene, of course you could have an explosion of an amplification in a cancer gene.”

McKernan added, “If you have lipid nanoparticles that are encapsulating this material, you now have a Trojan horse to get into the cells.”

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