516 Times More DNA Contamination in COVID Jab Than FDA Limit—SV40 Cancer Sequence and Risk of Human Genome 'Integration': French Study
Contamination found at 516 times the FDA and EMA legal limit of 10 nanograms per dose.
A French Government-funded study preprint submitted Tuesday and authored by Dr. Didier Raoult has confirmed that Pfizer Inc.’s COVID-19 injection contains 5,160 nanograms (ng) of contamination DNA per dose, exceeding the FDA and EMA’s regulatory safety limit of 10 ng per dose by 516 times.
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This alarming figure supports this website’s previous reports, as multiple studies analyzing different batches now suggest the jab’s DNA contamination may be more widespread than previously acknowledged.
In the new study, the contamination was first measured at 216 ng per dose, but after treatment with Triton-X-100—a chemical used to release trapped DNA—the levels surged by 24 times, revealing the staggering amount of residual DNA in the final product.
“Vaccine plasmid DNA quantification using the Qubit fluorometer on a vaccine vial showed it was 216 ng/dose on average and approximately 24 times greater, reaching 5,160 ng/dose on average, after treatment with Triton-X-100,” Dr. Raoult explained.
The study also identifies sequences linked to the vaccine’s manufacturing process, including an SV40 initiation factor.
This component, used to aid replication in laboratory settings, underscores failures in the purification process.
What Does the Study Say About SV40?
Dr. Raoult’s study identified several components of the plasmid DNA used during Pfizer’s vaccine manufacturing process, including a bacterial origin of replication, an antibiotic resistance gene, and an SV40 initiation factor.
The SV40 sequence is part of the manufacturing plasmid, used allegedly to facilitate DNA replication in laboratory processes.
According to the study, the plasmid “notably contains an active bacterial origin of replication, an initiation factor of the SV40 virus… and a gene of resistance to kanamycin.”
Kanamycin is an antibiotic used to treat bacterial infections and as a resistance marker in genetic engineering.
SV40, or Simian Virus 40, is a virus originally discovered in monkeys and later associated with potential cancer risks in humans.
It became infamous in the mid-20th century when it was found in some polio vaccines.
SV40 is linked to brain tumors, bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma.
The SV40 initiation factor mentioned in this study is not the virus itself but a genetic sequence used to enhance plasmid replication during the manufacturing process.
However, its detection in residual DNA fragments highlights a failure in the purification process.
This suggests that components of the manufacturing plasmid, including the SV40 initiation factor, may have made their way into the final vaccine product.
How Much DNA Was Found?
The study measured DNA contamination at 216 ng per dose, far exceeding the legal limit of 10 ng per dose set by the U.S. Food and Drug Administration and European Medicines Agency (EMA).
After treating the sample with Triton-X-100, the amount skyrocketed to 5,160 ng per dose, representing a 24-fold increase.
This final measurement exceeded regulatory limits by 516 times, a violation of safety standards.
Why Is This DNA Dangerous?
Residual DNA contamination poses risks, including the possibility of DNA fragments integrating into human genomes.
“In DNA-based gene therapy, it was reported that a proportion of 10-20% of cells are usually transfected,” Dr. Raoult noted, with “1-10% of the transiently transfected cells [becoming] stably transfected.”
“These results...raise issues regarding a putative risk of its integration in the human genome after its entry into cells,” Dr. Raoult warned.
The inclusion of the SV40 initiation factor in the manufacturing plasmid underscores the need for stringent purification, as sequences designed for replication should not remain in the final product.
While the study does not confirm adverse health effects, it raises serious concerns about manufacturing safety.
How Did This Happen?
Dr. Raoult suggests systemic failures in Pfizer’s manufacturing process allowed these contaminants to remain in the final product.
The plasmid DNA, designed for use only during production, should have been fully removed during purification. Instead, the study found “abundant presence of DNA” in tested batches.
“There may be variability from one batch to another, and this requires regular quality controls on the different batches,” Dr. Raoult emphasized.
Without consistent oversight, similar contamination could persist in future batches.
What Needs to Happen Now?
Dr. Raoult calls for urgent global testing of vaccine batches to assess the scale of contamination.
“Previous findings warrant to be confirmed at a larger scale, which is technically very easy to perform,” he stated.
The study underscores the urgency of regulatory reforms to protect public safety.
Independent laboratories must verify these findings and enforce stricter manufacturing and purification standards.
Public Trust Demands Accountability
The discovery of 516 times the legal DNA limit and the presence of manufacturing sequences such as the SV40 initiation factor highlights significant lapses in vaccine production safety.
While the SV40 sequence is linked to the manufacturing process, its mention emphasizes the consequences of incomplete purification and quality control.
Regulators like the FDA and EMA must act swiftly to address these failures.
Without transparency and accountability, public trust in medical products and regulatory systems will continue to erode.
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The Food and Drug Association DOES NOT TEST 'vaccine' products for ingredient values, product efficacy, nor any "safety" parameters and never has. >>> There is no legal limit to the amount of so-called contamination that can legally be included in vaccines or any other biological products. >>> Part 8 of series. >>> KATHERINE WATT >>> MAY 21, 2024
https://bailiwicknews.substack.com/p/there-is-no-legal-limit-to-the-amount
European Medicines Agency 'vaccine' policies are much the same. Relying on manufacturers to disclose *actual* product ingredients and manufacturing practices has gotten to where we are today.
Engineering and deployment of ALL genetically modified materials needs to be criminalized and Banned world wide. Denying obvious facts is a death wish...
Why not just outright outlaw these damnably dangerous "medicines?" We already have research proving they do NOTHING to protect against COVID. Every other country has done reliably honest studies searching for The Truth, and those looking for it can't unsee it. Why not here in the U.S. of A. (as if we don't already know...)??