Dr. Robert Malone, the inventor of mRNA and DNA vaccines, slammed health regulatory agencies for not informing people about potential plasmid DNA contamination in mRNA COVID-19 vaccines.
Talking about the study in a Nov. 11 Substack post, Dr. Malone said that plasmid DNA contamination in the vaccines is a "Proven fact" that has been "Acknowledged by the US FDA, Health Canada, and the European Medicines Agency."
The FDA's 2009 "Guidance on Prophylactic DNA Vaccines: Analysis and Recommendations" states that concerns about plasmid DNA potentially integrating into the genome of the vaccine recipient and increasing the likelihood of issues like "Malignant transformation, genomic instability, or cell growth dysregulation" were raised when DNA vaccines were initially introduced for clinical use.
Dr. Malone noted that the FDA has issued a "Categorical denial of adulteration and risk" of DNA vaccines.
It isn't clear whether the presence of the SV40 sequence in the plasmid DNA of mRNA vaccines was identified by Pfizer when the company applied for approval from the FDA. Dr. Malone pointed out that Moderna "Clearly acknowledges" the risks of genotoxicity associated with the DNA delivered via its vaccines.
"The only objective conclusion to be made concerning such statements is that they functionally represent propaganda rather than proven scientific and regulatory fact." FDA's 'Willful Blindness' In his Substack post, Dr. Malone called the FDA's assertion of "No safety concerns" about the inclusion of residual DNA in mRNA vaccines "Willful blindness." He then highlighted the risks posed by residual DNA in vaccines.
In the case of the mRNA COVID-19 vaccines, the SV40 enhancer gene and other genetic sequences were introduced in the plasmid DNA. Once the mRNA and DNA are harvested from the bacteria, the DNA is supposed to be removed.
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