Florida’s Surgeon General Reports Detection Of DNA Fragments In Covid MRNA Vaccines – My Comments
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[I can't believe the surgeon general of Florida is a Black. Are you telling me he's the most qualified guy for that position in all of Florida? I very much doubt that. Jan]
The Florida Surgeon General, Dr. Joseph A. Ladapo, is demanding answers from Dr. Robert M. Califf, the Commissioner of the U.S. Food and Drug Administration (FDA), regarding the detection of host cell DNA fragments in mRNA COVID-19 vaccines developed by Pfizer and Moderna.
The Florida Surgeon General sent a letter to FDA Commissioner Califf and CDC Director Mandy Cohen on December 6, pressing for greater transparency about the potential for DNA integration into the human genome—a concern that could have far-reaching implications.
The Florida Public Health Integrity Committee discussed these issues on November 14, 2023, and Ladapo urged the FDA to consider their findings. In addition, he reminded Califf of a previous communication dated May 10, 2023, which had yet to receive a response.
On May 10, Ladapo sent a letter to Califf and former CDC Director Rochelle Walensky regarding the risks of the experimental COVID-19 vaccines.
The letter reads:
Your ongoing decision to ignore many of the risks associated with mRNA COVID-19 vaccines, alongside your efforts to manipulate the public into thinking they are harmless, have resulted in deep distrust in the American health care system. Beginning with Operation Warp Speed, and possibly to be continued with an additional $5 billion investment in Project NextGen, the federal government has relentlessly forced a premature vaccine into the arms of the American people with little to no concern for the serious adverse ramifications.
Data are unequivocal: After the COVID-19 vaccine rollout, the Vaccine Adverse Events Reporting System (VAERS) reporting increased by 1,700%, including a 4,400% increase in life-threatening conditions. We are not the first to observe such a trend. Dismissing this pronounced increase as being solely due to reporting trends is a callous denial of corroborating scientific evidence also pointing to increased risk and a poor safety profile. It also fails to explain the disproportionate increase in life-threatening adverse events for the mRNA vaccines compared to all adverse events.
In the letter sent last week, Ladapo raised alarms about potential nucleic acid contaminants in the Pfizer and Moderna COVID-19 mRNA vaccines, particularly those in combination with lipid nanoparticles and the identified Simian Virus 40 (SV40) promoter/enhancer DNA.
“Lipid nanoparticles are an efficient vehicle for delivery of the mRNA in the COVID-19 vaccines into human cells, and may therefore be an equally efficient vehicle for delivering contaminant DNA into human cells. The presence of SV40 promoter/enhancer DNA may also pose a unique and heightened risk of DNA integration into host cells,” wrote in the letter.
The 2007 FDA guidelines warn of the potential for DNA integration to impact oncogenes and cause chromosomal instability.
The COVID-19 mRNA vaccines, with their lipid nanoparticle delivery system, ostensibly increase the risk of DNA fragment integration into the human genome. The letter states:
DNA integration could theoretically impact a human’s oncogenes – the genes which can transform a healthy cell into a cancerous cell.
DNA integration may result in chromosomal instability.
The Guidance for Industry discusses biodistribution of DNA vaccines and how such integration could affect unintended parts of the body including blood, heart, brain, liver, kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, the site of administration and subcutis at injection site.
Surgeon General Ladapo’s letter concluded with a trio of pertinent questions for the FDA:
Have drug manufacturers evaluated the risk of human genome integration or mutagenesis of residual DNA contaminants from the mRNA COVID-19 vaccines alongside the additional risk of DNA integration from the lipid nanoparticle delivery system and SV40 promoter/enhancer? Has FDA inquired any information from the drug manufacturers to investigate such risk?
Do current FDA standards for acceptable and safe quantity of residual DNA (present as known contaminants in biological therapies) consider the lipid nanoparticle delivery system for the mRNA COVID-19 vaccines?
Considering the potentially wide biodistribution of mRNA COVID-19 vaccines and DNA contaminants beyond the local injection site, have you evaluated the risk of DNA integration in reproductive cells with respect to the lipid nanoparticle delivery system?
Given the widespread use of these vaccines, Ladapo urged a rapid response. He requested written answers by December 13, 2023, stating that the American people and scientific community deserved transparency on this matter to inform their decisions about the vaccines.
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