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A recent paper suggests that COVID vaccines may meet the multi-hit hypothesis for cancer. According to the paper, the vaccines affect the p53 and BRCA tumor suppressor systems, impair DNA repair, and contain DNA fragments with cancer-promoting properties. The presence of SV40, a known cancer promoter, in the vaccines further supports this hypothesis. While it is important to note that this applies to some individuals, it suggests a potential link between the vaccines and cancer development.

The SB40 sequence was not declared to regulators and poses a potential cancer risk because any DNA that promotes cell growth can lead to unregulated cell growth, which is cancer. Concerns have been raised about the link between the vaccine and cancer. It is crucial to study and sequence cancers that have developed after vaccination to determine if there is a connection. This remains an important unknown that needs urgent investigation.

Kevin McKernan recently discovered that there is contamination in the mRNA shots with cDNA, including a cancer-promoting segment called SV40. SV40 turns on cancer genes in the human body and impairs tumor suppressor systems. This means that the shots not only promote cancer through SV40 but also inhibit our ability to fight cancer. The increase in cancer rates is undeniable, but the question remains: how much of this is due to the vaccines?

The Pfizer and Moderna vaccines contain fragments of DNA, which can integrate into the genomic DNA of cells and become a permanent part of the cell. This poses a potential risk of autoimmune attacks and future cancer. The DNA contamination occurred during the production process, where a plasmid vector was used to scale up the production of the RNA template. The regulatory threshold for DNA in vaccines is outdated and not suitable for this new type of vaccine. The speaker believes that DNA sequencing should be done on vaccinated individuals' stem cells to determine if this theoretical risk has occurred. Informed consent is necessary, and the lack of transparency regarding the DNA contamination is concerning.

The presence of DNA plasmids and undisclosed proteins in the Pfizer COVID-19 vaccine has raised concerns. The DNA plasmids, originating from E. Coli, were not properly removed during manufacturing, resulting in contamination. Additionally, two proteins from the simian virus 40 (SV40) were found in the vaccine, which is associated with certain cancers. SV40 was present in polio vaccines administered to millions of Americans in the past. Injecting these proteins and DNA into the body can potentially lead to mutations and increased risk of cancer. This discovery suggests a higher chance of mutation from the Pfizer COVID-19 vaccine.

The speaker claims SV40 in literature turns on cancer genes. They further claim the spike protein impairs tumor suppressor systems P53 and BRCA, promoting cancer and inhibiting the ability to fight it. The speaker suggests cancer rates are up, and the question is how much is due to vaccines. They state that repeated shots every six months increase the chances of getting loaded with synthetic genetic material that will cause harm, including heart disease, neurologic disease, blood clotting, immunologic problems, and cancer.

When COVID-19 vaccines were sequenced, commercial annotation software highlighted functional parts of the plasmids, including antibiotic resistance genes and SV40 components. The speaker claims that Pfizer had to manually remove these annotations before submitting the plasmid map to regulators. According to the speaker, regulators received the DNA sequence, but the sponsor is obligated to annotate every open reading frame and promoter, even if their function is unknown. The speaker alleges that Pfizer intentionally removed annotations, hiding them from the FDA, which the speaker believes is a violation of guidelines. The speaker suggests the reason for hiding SV40 components is due to SV40 virus contamination in polio vaccines and its debated link to cancer. The speaker asserts that while epidemiological data is confounded by vaccine shedding, laboratory studies show SV40 is a potent oncogenic virus. The speaker claims that the vaccines contain some of the more carcinogenic components of that virus, and that these sequences are functional and have consequences.

An article in Spectator Australia reported that DNA plasmids are contaminated with SV40 promoter sequences, which are oncogenic and used in cancer development in mice. The speaker questions why this is in an RNA vaccine, as the presence of DNA means it can integrate. Despite claims that the spike protein stays at the injection site, it has been identified everywhere, including in metastases from a colorectal cancer case where spike messenger RNA from the vaccine insertion was confirmed. The speaker was refused autopsies, even with consent from relatives, including a case of explosive melanoma after a booster shot. A report in The Lancet about deaths after vaccines was pulled, allegedly due to improper peer review. The speaker claims a media channel warned them that the government had made it a crime to criticize the vaccine program on the media.

COVID-19 vaccines, especially mRNA ones, may promote cancer through impairing DNA repair, inhibiting tumor suppressor systems like p53 and BRCA, and containing DNA impurities. These impurities include fragments from circular DNA used in the manufacturing process, such as SV40, a known proto-oncogene activator. The vaccines could potentially initiate or accelerate cancer growth by weakening natural tumor surveillance systems. This phenomenon is referred to as "turbo cancer."

A biochemist and toxicologist discusses concerns about the Pfizer vaccine. They claim that the vaccine contains plasma DNA, including SV40 sequences, which were not disclosed to regulators. They believe this is intentional and could lead to DNA integration and potential cancer risks. The speaker argues that the DNA in the vaccine is different from RNA and can be permanent. They suggest that safer alternatives like hydroxychloroquine and ivermectin exist and question the transparency of the FDA. They urge states to protect their citizens and reconsider the use of the vaccine, especially for pregnant women and children.

The speaker claims messenger RNA vaccines with the spike protein can induce cancer in multiple ways. They allege the presence of oncogene stimulants, specifically SV40 in the Pfizer vaccine, confirmed by multiple researchers. A paper from Wurzburg purportedly confirms this and shows the vaccines convert cells to cancer. The speaker asserts the spike protein and mRNA vaccines bind to major suppressor genes like P53, BRCA, and MSH, which normally suppress cancer. Mutations in these genes can lead to earlier onset of cancer. The speaker suggests these vaccines could cause the equivalent of mutations in these genes, leading to an explosion of colorectal cancers. They advocate for an immediate ban on these vaccines and accountability for those who oppose it.

The speakers discuss how initial kidney cells from monkeys used to make vaccines inadvertently gave people simian virus 40, which can lead to rapid cancer. One speaker says that this is one of the cancer-causing issues with the shots, explaining that it's supposed to stay out of the nucleus but can get in. One speaker says the initial claim was that the shot would stay local, in the arm, and dissipate quickly, but "they know that's not true." The other speaker mentions pseudouridine, a replacement nucleotide that is hard to break down, and that there's no study showing that it can be cleared from the body. This could be why some people have high antibody levels years later.

In this video, the speakers discuss new information about the mRNA vaccines and the presence of DNA in them. Researchers have found that some mRNA vaccines contain DNA fragments, which can cause issues with gene expression and potentially increase the risk of cancer. The presence of DNA in the vaccines is a manufacturing problem, and it is unclear why it was included. The DNA can enter cells and interfere with important genes, leading to various health problems. The speakers emphasize the need to investigate the extent of DNA contamination in the vaccines and consider stopping their production until the issue is resolved.

The speaker explains that there is contamination in the messenger RNA, including fragments of DNA called cDNA, with one of them being s v 40, a known cancer-promoting segment. The other speaker mentions that mainstream news reports estimate that millions of Americans had cancer due to SV 40 contamination in the past. The first speaker confirms that SV 40 turns on cancer genes and that the spike protein in the shots impairs tumor suppressor systems. They conclude that the shots promote cancer through SV 40 and suppress our ability to fight cancer. The speaker acknowledges that cancer rates are increasing, but the extent to which vaccines contribute to this is still uncertain.

The speaker states they found four pieces of the virus, not the whole virus. The pieces found include the SV40 origin of replication, the SV40 promoter, the SV40 enhancer, and part of the poly A signal. The speaker claims David Dean published that the SV40 enhancer is a nuclear targeting sequence. Therefore, claims that it will not reach the nucleus are inaccurate. The speaker asserts the presence of the SV40 origin of replication, a mammalian origin of replication, means it will replicate inside mammalian cells. The speaker believes regulators need to consider this risk.

Kevin McKernan discovered DNA contamination in Pfizer vaccines, specifically the simian virus 40 (SV40) promoter, which is known to cause cancer. This finding has been supported by other researchers and indicates a rise in aggressive cancers, with patients experiencing rapid tumor growth. Anecdotal evidence suggests a correlation between COVID-19 vaccinations and sudden cancer diagnoses, including cases of lymphadenopathy and breast cancer following vaccination. The SV40 is linked to both oncogenesis and angiogenesis, which is essential for tumor growth. Reports show significant increases in lymph node and bone marrow cancers, indicating a troubling trend in cancer rates post-vaccination.

The speaker expresses concern about the presence of SV40 sequences in vaccines, suggesting that their integration into certain genetic areas could potentially cause cancer. They mention the risk of insertional mutagenesis and the delay in bringing gene therapies to market due to this concern. The speaker also advocates for the use of alternative treatments like hydroxychloroquine and ivermectin, stating that they are safe drugs. They question the transparency of the FDA in redacting data and holding clinical data for 75 years. The speaker urges the protection of citizens and calls for one state to take the lead in doing the right thing. No questions are asked.

Research has shown that COVID vaccines are contaminated with DNA, including a cancer virus promoter sequence. The DNA can enter the human genome, potentially activating carcinogenic genes and increasing cancer risk. Vaccines suppress immunity, further raising cancer risk. The presence of DNA in vaccines can lead to long-lasting spike production, causing health issues. Vaccines inducing IgG4 antibodies are considered defective. DNA impurities in vaccines can intensify side effects. DNA should not be introduced into the body's cells.

The speaker discusses the presence of contamination in vaccines, specifically cDNA fragments and s p 40, which is a cancer-promoting segment of DNA. They mention that s v 40, a related virus, caused cancer in millions of Americans in the past. The speaker explains that s p 40 turns on cancer genes and that the spike protein in the vaccines impairs tumor suppressor systems. They conclude that the vaccines promote cancer and hinder our ability to fight it. The speaker acknowledges that cancer rates are increasing but questions how much of it is due to the vaccines.

Lipid nanoparticles (LNPs) can deliver mRNA and DNA to various cells, potentially leading to cancer by promoting the spread of existing cancer cells and possibly having oncogenic effects. The SV40 promoter in plasmids can amplify cancer genes, and the spike protein may inhibit tumor suppressor p53. Insertional mutagenesis can create aberrant proteins linked to cancer. mRNA can reverse transcribe to DNA and integrate into the genome, especially in ovaries and testes. Immunosuppression of T cells can allow cancer expansion. Genetic vaccines might be passed to offspring through sperm or ova, raising concerns about contaminating the gene pool. There is a lack of investigation into whether these genetic elements integrate into germ cells, which could lead to cancer through genomic integration rather than functional integration.

The panel discusses replication (replicon) vaccines and their potential dangers, focusing on how they differ from conventional messenger RNA (mRNA) vaccines and what new risks might emerge as this technology develops. Key points and concerns raised - Replicon vaccines concept and fundamental differences - Replicon vaccines use replication-capable genetic material, so the embedded genetic information not only makes antigen proteins but also multiplies inside the cell. They are described as having both constitutive function (the ability to make proteins) and, crucially, the capacity to replicate, which distinguishes them from traditional, non-replicating mRNA vaccines. - It is explained that replication introduces additional mutation and recombination opportunities, because the RNA genome is copied more than once, and the process can produce variants that differ from the original design. - Central dogma exceptions and viral biology - The speakers explain that while the central dogma (DNA → RNA → protein) generally governs biology, some viruses violate this, with RNA viruses that replicate via RNA-dependent replication and even some reverse-transcribing retroviruses that convert RNA to DNA and integrate into genomes. This context is used to frame why replicon vaccines could behave unpredictably. - Potential risks of replication and spread - A core concern is that the replicon approach might allow the vaccine genome to spread beyond the initial target cells, potentially reaching other cells and tissues, or even spreading to other people via exosomes or other means. Exosomes can transport DNA, RNA, and proteins between cells; thus, the replicon genome could in theory be disseminated. - The possibility of homologous or heterologous recombination between replicon genomes and wild-type viruses could yield new variants. The panel emphasizes the difficulty of controlling such recombination in a living system. - Specific material and design considerations - The use of viral components like spike protein genes in replicon vaccines raises concerns about how these proteins might mutate or recombine during replication, potentially altering antigen presentation or safety. - A concern is raised about the lack of repair mechanisms in RNA replication (as opposed to DNA replication), which could make error rates higher and lead to unpredictable changes. - The panel notes that current replicon vaccine designs (including those using alphavirus backbones) inherently carry high mutation and recombination risk, and that the replicating systems may encounter unpredictable evolutionary dynamics inside the human body. - Safety signals and clinical anecdotes - The speakers cite cases of adverse events temporally associated with vaccines, including vascular inflammation and thrombosis, stroke-like events, and myocarditis, to illustrate that immune responses to vaccines can be complex and occasionally severe. They emphasize that such observations do not establish causality, but argue they warrant careful scrutiny. - There are references to cases of acute vascular and neural complications following repeated vaccination, and to broader immune dysregulation phenomena, including IGG4-related disease and immune dysregulation syndromes that can involve multiple organs. - One example concerns a patient who developed sudden limb problems after the third dose, requiring surgery; another describes myocardial involvement after multiple doses and subsequent inflammatory sequelae. - DNA contamination and analytical findings - Kevin McKernan’s analysis of certain Japanese CoronaVac vaccines is cited: both DNA contamination and the presence of SV40 promoter elements were detected in some vaccine lots, with DNA amounts exceeding some regulatory benchmarks in at least one case. The concern is that DNA contamination, or the presence of promoter sequences, could influence integration or expression in unintended ways. - It is noted that vaccines using lipid nanoparticles can potentially deliver nucleic acids into cells; in the presence of exons or promoter sequences, there could be unintended cellular uptake and expression. - Implications for public health and policy - The panel underscores the need for caution, thorough investigation, and long-term observation of any replication-based vaccine platform before broad deployment. There is a call to evaluate risks, monitor long-term outcomes, and consider the possibility that replication-competent constructs could drive unforeseen evolutionary dynamics within hosts or communities. - There is contention about how information is communicated to the public, with particular emphasis on avoiding misinformation while ensuring that scientific uncertainties are transparently discussed. - Broader scientific context and forward-looking stance - The speakers discuss how the field’s approach to gene-based vaccines is evolving rapidly, and they stress that the compatibility of replicon systems with human biology is not yet fully understood. - They frame their discussion as not merely about current vaccines but about the trajectory of vaccine platforms: if replication-based or self-dispersing systems prove too risky or unpredictable, the prudent path might be to favor conventional, non-replicating strategies until safety, efficacy, and containment of unintended spread are more firmly established. Closing and takeaways - The session closes with emphasis on careful evaluation of replicon vaccines, awareness that viral genetics can behave differently in humans than in theory, and a call for continued discussion, independent verification, and transparent communication as the technology develops. - Throughout, speakers acknowledge the complexity of immune responses to vaccines, the potential for unexpected adverse events, and the importance of safeguarding public health while advancing vaccine science.

The Pfizer vaccine is contaminated with plasma DNA, not just mRNA. This DNA is the DNA vector used as the template for the in vitro transcription reaction. This was discovered by sequencing vials of Pfizer vaccine from Colombia. It's surprising that there's any DNA in there. The speaker is alarmed about the possible consequences of this, including rare but serious side effects like death from cardiac arrest. Mixing DNA with a lipid complex allows it to enter cells and become a permanent fixture. This is a real hazard for genome modification of long-lived somatic cells, like stem cells, and could cause a sustained autoimmune attack. There is also a very real theoretical risk of future cancer in some people. The risk is not zero and it may be high enough that we ought to figure out if this is happening or not.

Speaker 1 expresses concern about the presence of SV40 sequences in vaccines, suggesting it is not accidental and could lead to cancer due to insertional mutagenesis. They argue that gene therapies were delayed due to the risk of cancer from insertional mutagenesis. The speaker believes that alternative treatments like hydroxychloroquine and ivermectin are safe and questions why the FDA redacted data on endotoxin levels for 75 years. They emphasize the unusual nature of the current situation and urge the protection of citizens by not administering experimental products to pregnant women and babies. The speaker pleads for one state to take a stand and set an example for others. No questions are asked.

The SV40 sequence in the vaccine was undeclared and raises cancer concerns because any DNA sequence that instructs cells to replicate carries a hypothetical risk of causing unregulated cell growth, which is cancer. It is claimed that cancers appearing post-vaccination should be sequenced and studied to determine if the SV40 sequence is causing them. This sequencing and study has not yet occurred, and is a critical step in understanding the potential link between the vaccine and cancer.

The speaker explains that the messenger RNA in the shots is contaminated with cDNA, including a cancer-promoting segment called s v 40. They mention that s v 40 turns on cancer genes in the human body and that the spike protein in the shots impairs tumor suppressor systems. The speaker suggests that the shots promote cancer through s v 40 and inhibit our ability to fight cancer. They also mention that cancer rates are increasing. The speaker raises the question of how much of this is due to the vaccines.