reSee.it - Related Video Feed

There are concerns about the long-term side effects of modifying DNA and RNA to enable the production of antibodies. The potential for causing mutations or other risks in the future is uncertain.

The speaker expresses caution regarding the long-term side effects of modifying people's DNA and RNA. They state there is a risk associated with directly encoding the ability to produce antibodies into a person's DNA and RNA. The speaker is concerned about potential mutations or other downstream risks.

"Packaged DNA fragments have been found en masse as vaccine contaminants." "Once they reach the nucleus, short DNA sequences have an increased propensity to insert into chromosomal DNA." "The possible consequences are unending." "Disruption of the exquisitely tuned network that controls cell division and differentiation can lead to cancer and to developmental defects." "Mutations in sperm and fertilized egg cells could render altered traits inheritable." "Cost effective procedures to reliably separate mass produced RNA from plasmids do not exist." "Contamination of RNA vaccines with plasmid DNA must therefore be expected to be the rule and not the exception." "Whoever propagates RNA vaccines as being safe and effective, whoever claims that nothing can happen to your genome, is either incredibly ignorant or endlessly evil."

The symposium covers the potential safety and threat of “replicating” vaccines, especially LepriCon (leprecon) vaccines, in the context of Covid-19 vaccines and genome‑editing concepts. The speakers present a chain of claims and concerns, some drawing on reports and others presenting theories about how these next‑generation vaccines could behave in humans and populations. Key points and claims presented - Emerging mechanisms and risks: The panel notes that blood vessel inflammation and thrombosis mechanisms are increasingly observed, including in vaccine contexts, with examples from individuals who needed limb amputation and others who developed severe vascular events after vaccination. One case involved a 70‑year‑old man who, after a third dose, developed embolic events necessitating shoulder joint surgery, and another where a 60‑year‑old man developed acute limb ischemia and died; both are presented as suggesting a serious vascular mechanism linked to vaccination, though causal connections are not established. - Replicating/vector vaccines and their concerns:荒川博士 and others discuss LepiCon vaccines as vaccines that replicate inside the body. The concept involves “replicating viral vectors” where the genome can mutate and evolve during replication. The green‑highlighted segment in a slide (the antigen gene) plus a blue/orange segment (replicating gene cassette) is used to describe how LepriCon vaccines are designed to carry viral genes and replicate, with the assertion that replication, mutation, and recombination can occur, potentially generating new variants inside the host. - Differences from conventional vaccines: The discussion contrasts LepriCon vaccines with standard mRNA vaccines. In conventional mRNA vaccines, messenger RNA is delivered and translated into antigen proteins, then degraded; in LepriCon vaccines, replicating RNA/DNA can persist and continue producing antigen, with mutation and recombination possible. The panel emphasizes that LepriCon vaccines use replicating/copying mechanisms and that the genetic material can be copied in ways that differ from natural human biology, potentially creating unpredictable variants. - Central dogma and exceptions: The speakers reference the central dogma (DNA → RNA → protein) but note exceptions in viruses, including RNA viruses that can reverse‑transcribe to DNA (retroviruses) and RNA viruses that replicate RNA directly. They discuss how LepriCon vaccines would rely on replicative processes that do not follow the usual linear flow and why this could complicate predictions about safety and behavior in humans. - Potential for unintended spread and environmental impact: A major concern raised is that self‑replicating vectors could spread beyond the vaccinated individual, via exosomes or other intercellular transport, creating secondary infections or non‑target spread. Exosomes could ferry replicating genetic material, raising fears of new infection chains or “outbreaks” stemming from the vaccine itself, and even suggesting the possibility of vaccination‑induced spread akin to an attenuated or modified pathogen. - Safety signals and immunology concerns: The discussion touches on immune system risks, including immune dysregulation, autoimmune phenomena, and unexpected inflammatory responses. IGG4‑related disease is highlighted as a potential adverse outcome post‑vaccination, with descriptions of glandular and systemic involvement and the idea that high IGG4 levels could have immunosuppressive effects that alter responses to infection or vaccination. The panel notes observed increases in certain immunoglobulin subclasses after multiple LepriCon doses and discusses the possibility of immune tolerance or enhanced immune responses that could be harmful. - Historical and theoretical context: References are made to past epidemics and speculative pandemics caused by misused or dangerous vaccine platforms, drawing on central molecular biology concepts and historical anecdotes about how vaccines can be designed and misused. The discussion frames LepriCon vaccines as a high‑risk platform that could, in theory, generate recombinants, escape mutations, or cause unintended immune and inflammatory consequences. - Clinical and regulatory implications: The speakers call for caution, arguing that more evidence is needed before approving or widespread use of LepriCon vaccines. They emphasize the need for long‑term observation and transparent communication about risks, and criticize the potential for insufficient understanding among healthcare workers and the public. They also urge that any future vaccine development should consider the possibility of genome editing, recombination, and exosome‑mediated spread, and stress the importance of not underestimating possible adverse effects. - Real‑world observations and skepticism about hype: Several speakers underscore that the danger is not merely hypothetical; there are reports of adverse events, including stroke‑like conditions, inflammatory diseases, and immune dysregulation in vaccinated individuals. They stress that the evolution and mutation of replicating vaccines could outpace current surveillance methods, and that “information manipulation” or lack of transparent reporting could mislead the public about risks. - Final reflections and call to action: The concluding messages advocate recognizing the potential failures of messenger RNA vaccines and acknowledging that both conventional and replicating platforms may carry risks. The speakers urge ongoing critical analysis, cautious progression, and robust verification of claims through transparent, independent investigation. They close with thanks to the organizers and a hope that the discussion may contribute to broader public awareness and informed decision‑making. Notable emphasis and unique considerations - The core concern centers on LepriCon vaccines’ replication, mutation, and potential to spread beyond the vaccinated person; exosome transport and genomic/cellular integration are highlighted as mechanisms that could generate new risks not present with non‑replicating vaccines. - The discussion stresses that IGG4 responses could become alarmingly high after certain doses, potentially leading to immunosuppressive effects or autoimmune phenomena, and presents IGG4‑related disease as a potential complication to monitor. - The speakers insist that safety and transparency are paramount, and that misinformation or optimistic narratives about rapid vaccine development could lead to harm if new platforms are adopted without comprehensive evaluation. Overall, the symposium foregrounds cautious scrutiny of replicating vaccine platforms, frames potential biological and regulatory risks, and calls for careful, evidence‑based assessment before broader deployment.

Integrating foreign genes into chromosomes can lead to cancer and other health issues, permanently altering genetics and affecting future generations. This is a call to recognize the dangers posed by RNA vaccines being introduced globally by organizations like the WHO, CDC, and FDA. The initial vaccines have already shown harmful effects due to the introduction of foreign genes into the body. The production of mRNA does not ensure that these genes, often derived from bacteria, won't enter human cells. As a result, individuals receiving these vaccines may experience genetic alterations, and any genetically altered cell is at risk.

Speaker 0 asks: "Do you think there's evidence that the changes to people to their genetic structure wrought by these vaccines could be passed on to their children?" Speaker 1 responds: "The McCullough Foundation, of which I am the vice president, we just published a person who had cancer of the bladder, which is a very severe cancer, in that tumor, so in the bladder cells that had become dysplastic, that messenger RNA was found in the cancerous cells of this tumor. So it seems to be integrating. Now the question is, is it integrating in a way that is can be passed on to the offspring, or is it so dysfunctional that it's killing the host before it can be passed on? And and I don't know that we yet know that, but remember, the science is the topography of ignorance. I mean, there's a lot about this that is is very, very concerning. There's also a study that this messenger RNA seems to have transcribed into liver cells."

There are concerns about the long-term effects of modifying people's DNA and RNA to encode the ability to produce antibodies. The potential risks include mutations and other unknown consequences.

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 mRNA in vaccines can replicate, including the replication engine, leading to potential spread from person to person. Concerns exist about the inability to stop this replication, with unknown consequences for humanity. The spike protein in these vaccines can be toxic, affecting various tissues. Deployment of this technology in vaccines for humans is already happening, with over 4,000 people injected in Japan.

The speaker expresses caution regarding the long-term side effects of modifying people's DNA and RNA. They state there are unknown risks associated with directly encoding the ability to produce antibodies into a person's DNA and RNA. The speaker is concerned about the potential for mutations or other downstream risks.

I'm Philippe Boucalt, a cancer genomics researcher at the University of South Carolina. I've sequenced the DNA in the Pfizer vaccine and found that it contains fragments of DNA. This DNA could potentially cause rare but serious side effects, such as cardiac arrest and future cancer risks. The regulatory process that allowed this contamination is concerning. The DNA could integrate into long-lived somatic cells and potentially cause autoimmune attacks or disrupt tumor suppressors. To produce the vaccine, they cloned the PCR product into a plasmid vector, which led to the contamination. We can easily measure the amount of this substance in the vaccine and should conduct further studies to understand its implications. The FDA should require Pfizer to remove the DNA from the vaccine.

The speaker cautions that we don’t know the long-term side effects of modifying people’s DNA and RNA to directly encode the ability to produce antibodies, and whether that causes other mutations or downstream risks.

Alden and colleagues found that Pfizer's genetic code can be integrated into the human genome within an hour in a cancerous cell line. This suggests that Pfizer and Moderna's genetic material might become a permanent part of human DNA. There is no study confirming or denying this possibility. The concern is that if eggs or sperm incorporate this genetic code, it could be passed on to future generations. This lack of research is seen as reckless and worrisome.

The Pfizer vaccine contains not only mRNA but also plasma DNA from the vector used in its production. I sequenced samples from two batches of the vaccine in Colombia and found this DNA, which raises concerns about potential health risks. This DNA could integrate into the genomic DNA of cells, leading to permanent changes. Such integration poses theoretical risks, including autoimmune responses and cancer, depending on where the DNA inserts itself in the genome. While these risks may be rare, they warrant investigation to understand their implications better.

Speaker 0 cautions about the long-term side effects of directly modifying a person’s DNA and RNA to encode antibodies. They raise concerns that such genetic or molecular modifications could lead to unforeseen consequences over time, including potential mutations or other risks that might arise downstream as a result of encoding these antibodies.

We don't fully understand the long-term effects of modifying DNA and RNA. Recently, Facebook announced it would remove false claims about COVID-19 vaccines, specifically those suggesting the vaccine changes DNA. However, a leaked tape reveals Mark Zuckerberg stating that the vaccine modifies DNA, which contradicts Facebook's own policy. This statement would likely result in censorship on the platform today. The concern remains about the implications of such modifications and the unknown long-term side effects.

The Pfizer vaccine may contain DNA in addition to mRNA, according to a researcher who sequenced the vaccine in their lab. The DNA is a vector used in the production of the mRNA. The researcher expressed concern about the potential consequences of this, including rare but serious side effects like death from cardiac arrest. The DNA could integrate into the genomic DNA of cells and become a permanent part of them, posing a risk of genome modification and autoimmune attacks. There is also a theoretical risk of future cancer depending on where the foreign DNA lands in the genome. The researcher believes further investigation is needed to determine if these risks are occurring.

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.

We are facing a significant threat from those who have the means to contaminate the entire human genome. The mRNA vaccines could potentially affect future generations, as the injected genetic material may remain dormant until the next generation tries to have children. With billions of people already vaccinated, including millions of women capable of giving birth, there is a concern that these vaccines could introduce never-before-seen mutations into the human species. The true impact will only be known when problems arise in the offspring and subsequent generations. This is the enormity of the problem we are confronting.

Philip Buchholz, a PhD in biochemistry and molecular biology and cancer genomics researcher at the University of South Carolina, describes himself as an expert on how the human genome can be altered and which alterations cause cancer. He emphasizes his skill in DNA sequencing and detecting foreign DNA pieces at very low levels, noting that his lab used these abilities during the pandemic to invent the spit-based COVID test. He asserts that the Pfizer vaccine is contaminated with plasma DNA, not just mRNA, and that this DNA is the DNA vector used as the template for the in vitro transcription reaction when producing the mRNA. He claims to have proven this by sequencing in his own lab. Regarding evidence in Columbia, he says a colleague in the College of Pharmacy was in charge of the vaccination program and kept every vial, including empty ones with a small amount left at the bottom. He states he received these vials and examined two batches from Columbia by sequencing, sequencing all the DNA in the vaccine to determine its content, and notes it is surprising that any DNA is present at all. He asserts this DNA can be identified and the mechanism of its presence inferred, and that he is alarmed about the regulatory process that allowed it. He explains that this DNA could cause rare but serious side effects, including death from cardiac arrest, noting there are cases of suspicious death after vaccination and that DNA is a plausible mechanism. He argues that this DNA can and likely will integrate into the genomic DNA of cells that were transfected with the vaccine, describing it as a permanent fixture in the cell and in its progeny indefinitely. He says this makes the DNA different from RNA because it can be permanent, posing a real hazard for genome modification of long-lived somatic cells like stem cells, and potentially causing a sustained autoimmune attack toward that tissue. He adds that while autoimmunity is not his field, the cancer risk is within his purview and it is a possibility.

Are there concerns regarding the side effects of medicines? Is safety testing necessary? We are administering genetically modified organisms through injections, particularly in young children.

Genetic vaccines are seen as unacceptable due to concerns about introducing transgenes through gene therapy. Messenger RNA vaccines can lead to off-target effects in various organs, including the ovaries, brain, liver, spleen, and bone marrow. Spike proteins have been detected in rashes over a year after vaccination, indicating ongoing spike protein production. The speaker personally chose not to get vaccinated, viewing it as a risky decision, and has avoided the flu shot for similar reasons.

I have concerns about modifying DNA and RNA to encode antibodies directly, as we don't know the long-term effects. There may be risks like mutations or other issues in the future.

Caution about long-term side effects of modifying people’s DNA and RNA to directly encode the ability to produce antibodies, and whether this could cause other mutations or downstream risks.

I'm skeptical about the COVID vaccine, especially the mRNA vaccines. I recently spoke with a top cancer expert in Britain who was very critical of the long-term effects of the Pfizer and Moderna vaccines. According to this expert, we may see a significant increase in cancer cases as a result of these vaccines. While I believe the vaccines saved lives, I question whether we had enough time to fully understand the potential long-term consequences.