The discovery of genetic material contaminants in the Covid-19 jabs raises serious concerns about quality control, informed consent, and potential genetic effects on the human race.
This article was the original source of this post, my intention was to simplify it, and hopefully render it more accessible. Ignasz deserves full attribution. Apologies for my oversight. Any subscriptions or contributions please make to him.
Kevin McKernan, an established scientist with expertise in genomic sequencing technologies, has discovered genetic material contaminants in Pfizer and Moderna's Covid-19 vaccines. McKernan's primary research is being published directly to substack for peer review, indicating RNA fragmentation in both brands and all lots but is particularly notable in Pfizer vials.
His substack is here:
The contaminants found in the vaccines are replication-competent dsDNA plasmids with antibiotic resistance, and they contain code for the spike protein as an artifact of the industrial manufacturing process of the mRNA payload. The formulation of the Covid gene therapies comprises LNP components, the mRNA payload, and the dsDNA plasmid contaminant. Kevin estimates there are billions of contaminants per injection.
Using qPCR and electrophoresis, McKernan has confirmed that the amount of DNA in samples is several orders of magnitude over the EMA's limit, and 20-35% of the shot contents is dsDNA plasmid contaminant that is replication-competent in human and bacterial cells. The sheer volume of contamination could drive host genome integration of dsDNA with unknown effects over unknown timeframes.
I recently raised my concerns in this tweet:
The plasmids could extend host spike production in the body for an unintended length of time, and their antibiotic resistance makes them hard to remove from the gut, exacerbating general antibiotic resistance in humans to neomycin and kanamycin. The plasmids could turn the human host into a breeding ground for plasmids and mRNA that may contain the spike coding, and the process by which the plasmids can replicate in bacteria carries a risk of endotoxin poisoning that can be harmful or fatal.
Moreover, there is either wilful neglect or a wilful tolerance of potential genetic effects on the human race, and this research was done privately and independently, with no support from regulators or manufacturers.
McKernan's research found evidence of contamination of expression vectors designed for plasmid amplification in bacteria in the Pfizer and Moderna vaccines that makes it impossible for patients to give adequately informed consent. Negative effects of the treatment, such as myocarditis and pericarditis, were not disclosed to patients.
The battle to protect our children needs to ramp up.
The narrow-epitope strategy used in the treatment focuses on a highly specific part of the virus, making it easy for the virus to mutate and evade the immune response, and ongoing analysis suggests that patients' overall immune system capability is being degraded. Patients being coerced into a cycle of taking more boosters is leading to a worsening degradation of their immune systems.
Quality control is seriously inadequate, and the fidelity of these treatments has not been proven. There are ambiguities about what exactly patients are being injected with. Manufacturer regulatory submissions are not publicly available, and manufacturers can potentially withhold clinical trial data from regulators. Supply contracts are confidential, but some have been partially leaked.
Pfizer only warrants that the product complies with the relevant specifications at the time of delivery, without specifying any performance criteria tied to trial results around efficacy. The MHRA has 24 hours from formal receipt to identify shortcomings in the product, including genetic information, but would need to be inspecting vial content in a fashion similar to that by Kevin McKernan to detect dsDNA contamination.
In conclusion, the discovery of genetic material contaminants in Pfizer and Moderna's Covid-19 vaccines raises serious concerns about quality control, informed consent, and potential genetic effects on the human race. There is a wilful neglect or tolerance of these issues, and patients taking more boosters only contributes to the degradation of their overall immune system capability. Moreover, there is a need for transparency and accountability in manufacturers' regulatory submissions and supply contracts to ensure public safety.
Great work Paul.
I have just asked Senator Rennick to demand full Bioburden and Endotoxin assay results from the TGA labs, not just "pass" or fail". We need the actual toxin numbers for each Lot or Batch tested in Australia to compare with that mandatorily reported in the manufacturer documentation. Have also asked British MP Andrew Bridgen if he can do the same.
Seeing as you aren't willing to credit me and have literally plagiarized my work, I'll credit myself, for my article published 3 hours before you lifted it:
Imitation is the highest form of flattery, but it's not worth paying for.