Unveiling the Genetic Time Bomb: The Cancer-Causing Contamination
German scientists Kammerer, Schulz, & Steger uncover shocking DNA contamination in Pfizer’s COVID-19 vaccines—up to 13 times over the limit—raising grave concerns about health and regulatory failures
The findings of Kammerer, Schulz, and Steger are not merely scientific observations—they are an indictment of a global system that has failed humanity. Their peer-reviewed study reveals a level of contamination in RNA-based COVID-19 vaccines that should shock anyone who placed trust in the institutions meant to protect public health. This is not a minor oversight, nor an isolated incident. It is a catastrophic failure with potential consequences for billions of individuals injected during 2021 and 2022.
A Bombshell Revelation
The study, published after five months of rigorous peer review, analyzed four German BNT162b2 vaccine lots, uncovering synthetic DNA contamination between 32.7 and 43.4 nanograms per dose. To put this in perspective, the upper permissible limit for naked DNA in vaccines is 10 nanograms per dose. This means the detected levels exceeded regulatory thresholds by four to five times. However, as highlighted by Kevin McKernan, this is likely an underestimation. When accounting for the limitations of the dyes used in testing, the contamination may reach an astronomical 133 nanograms per dose—thirteen times the legal limit.
This contamination is not inert. It includes the SV40 promoter/enhancer sequence—a known genetic element with a history of association with cancer-causing mechanisms. Its presence in the vaccine’s plasmid, despite being absent from regulatory filings, raises questions about the integrity of both the manufacturing process and the approval pathways. SV40 sequences are not accidental contaminants; they are purposefully engineered components that significantly increase the risk of DNA integration into human genomes.
The Silent Betrayal
What makes these findings more troubling is their global nature. Just last week, French scientists led by Didier Raoult reported similarly excessive synthetic DNA contamination in Pfizer’s vaccines distributed in France. Across continents, the story is the same: unsafe levels of synthetic DNA, potent lipid nanoparticles (LNPs) acting as transfection agents, and regulatory silence. This is not a regional issue; it is a global crisis. Every dose delivered during the peak of the vaccination campaigns in 2021 and 2022 carries this contamination, affecting billions of people.
The implications are staggering. Lipid nanoparticles are not inert delivery systems—they are engineered to smuggle genetic material into human cells. The contaminated DNA is not merely present; it is active. Studies have demonstrated that these DNA fragments can integrate into cellular genomes, producing spike proteins and potentially triggering long-term health consequences. Preliminary research has already identified genomic integration in ovarian cancer cell lines. These are not hypotheticals—they are real, documented risks.
Regulatory Complicity
This crisis is compounded by the complete abdication of responsibility by global health regulators. Agencies like the Therapeutic Goods Administration (TGA) in Australia and the European Medicines Agency (EMA) have consistently dismissed these findings as “misinformation” without offering any substantive rebuttal. Their inaction is not merely negligent; it is complicit.
Consider this: the TGA, which claims to uphold the highest standards of safety, approved these vaccines through expedited pathways designed for emergencies. These pathways bypassed long-term safety studies, and now, the consequences are becoming evident. When researchers like Kammerer et al. present irrefutable evidence of contamination and potential health risks, these agencies respond with silence or deflection.
This silence is not harmless. It protects manufacturers while leaving billions of people vulnerable to unknown health consequences. Worse, it perpetuates a system where accountability is nonexistent, and profit takes precedence over safety.
Unfathomable Health Consequences
What are the potential outcomes of this contamination? The answers are as terrifying as they are uncertain. Genomic integration could lead to a host of chronic conditions, including autoimmune diseases, genetic disorders, and cancers. The presence of SV40 sequences further exacerbates the risk, as these elements are designed to interact with human DNA in ways that could alter the very building blocks of life.
This is not just about the individuals injected during 2021-2022. The genetic alterations, if proven to be heritable, could affect future generations. Humanity is staring down a potential biological time bomb, and the silence from those responsible only amplifies the danger.
A Call to Action
The Kammerer study demands immediate, global action. Governments and health regulators must:
Suspend the use of RNA-based COVID-19 vaccines** until the full extent of contamination is understood and addressed.
Conduct independent analyses** of retained vaccine samples from early production lots to determine the scale of the issue.
Launch comprehensive health monitoring** for the billions already injected, with a focus on identifying and treating potential long-term effects.
Hold manufacturers accountable**, including forcing full transparency of production processes and regulatory filings.
But this is not enough. The very structure of global health governance must be reimagined. Regulatory agencies must be independent of pharmaceutical funding and influence. Expedited pathways must be scrutinized and limited to ensure public safety is never compromised for convenience.
The Fight for Humanity’s Future
This is not merely a scientific debate—it is a battle for the soul of humanity. The findings of Kammerer, Schulz, and Steger are not just data points; they are a warning. The health of billions and the trust in public health systems are at stake. This is a moment for courage, accountability, and action.
The silence of regulators and manufacturers is deafening, but it cannot be allowed to define the future. We must demand answers. We must demand justice. The stakes have never been higher.
"This contamination is not inert. It includes the SV40 promoter/enhancer sequence"...
"Its presence in the vaccine’s plasmid, despite being absent from regulatory filings, raises questions about the integrity of both the manufacturing process and the approval pathways. SV40 sequences are not accidental contaminants; they are purposefully engineered components that significantly increase the risk of DNA integration into human genomes."
Your paragraphs say it all Gaz... It's deliberate... It's no accident... Current cancer list in my social circle is huge... Especially brain tumours... Followed by bowel and pancreatic cancer, and at one B Cell lymphoma...
Four cases of cancer at my small workplace since I was given the boot for not wanting a genetic injection.
Two are dead within months, one had pancreatic cancer, the other had bowel cancer spread everywhere organs, lymph system...
Two are still alive, one a brain tumour... The other B Cell Lymphoma ..
My wife's small workplace has three cases too... One has brain tumour, another thyroid cancer and the other one bowel cancer.
My cousin's wife just passed, I sent to the funeral a week ago, leaves behind two devestated kids barely out of their teens... She had a rapidly progressing brain tumour.
I could list many heart and clot related complications in my social circle too... All post jab, and enough toake a lengthy Substack in and of itself.
Work still pushed a vac mandate despite a doctor confirmed vaccine pericarditis case.. OH&S rules out the door...
Unfortunately now all those families mentioned above are paying a terrible price, plausible deniability for the vax, but suspiciously coincidental with vax roll out...
The SV40 and plasmids were deliberate, not negligence, and therefore an attack on us all.
Has that dill Butler seen this or his flunky that he gets to do the hard yards?