PART II: Implications of plasmid DNA fragments in blood products
Blind spots in the oversight of blood products, leaves the public in a dangerous state of speculation.
@Kevin_McKernan @Jikkyleaksblog.maryannedemasi.com/p/part-ii-impl…
Gene fragments encoding 'SV40' and 'Kanamycin,' which are specific to the plasmid DNA used in vaccine manufacturing of mRNA vaccines, have been identified in blood samples.
If these genetic sequences can persist in the bloodstream after vaccination, and potentially end up in blood products such as fresh frozen plasma, whole blood, or cryoprecipitate, what risks might they pose to recipients?"
Australian Red Cross says there is no evidence risk to a recipient. But it does not track the COVID-19 vaccination status of donors, nor has it tested for these genetic components of mRNA vaccines in donated blood. @RedCrossAU
Dr Richard Davis, former member of the SA Red Cross blood transfusion committee, has questioned the robustness of these assurances.
“If the Red Cross is not documenting the vaccination status of donors, how can it possibly track any harm?”
“Further, the Red Cross should not claim there is no evidence of risk to recipients when such effects may take years to manifest,” he added.
As late as September 2022, American @RedCross stated on X, “the COVID-19 vaccine does not enter the bloodstream.”
But findings by Chakraborty, data from biodistribution studies in Japanese regulatory documents, and a study published this month in Nature, all clearly show that the vaccine leaves the injection site and circulates widely throughout the body.
“Without data, we are left in a dangerous state of speculation,” Dr Davis said.
PART 1: Blood samples contain foreign DNA sequences from COVID-19 mRNA vaccine
This 2-part series investigates synthetic DNA fragments unique to mRNA vaccines in blood samples, and the implications for the safety of blood products in Australia. @Kevin_McKernan @Jikkyleaks @P_J_Buckhaults
“The blood samples from people in South Australia contained large numbers of these foreign gene sequences which were not present before [mRNA] vaccination,” explained Professor Petrovsky.
These revelations have also prompted calls for accountability at the highest levels of government.
@BroadbentMP and 62 co-signatories are demanding an evidence-based response to restore public trust and ensure vaccine safety.
Evidence compiled by @Double_Christ & @katiebeenanddid
🚨FDA responds to study on DNA contamination in Pfizer Vaccine
The regulator says the study "does not belong to the FDA," and refuses to address the data that emerged out of its own lab, conducted by students under the supervision of FDA staff, using FDA resources.
@Kevin_McKernan @Jikkyleaksblog.maryannedemasi.com/p/fda-responds…
The @US_FDA doesn't address the involvement of three of its own scientists—Dr Shuliang Liu, Dr Tony Wang, and Dr Prabhuanand Selvaraj—who supervised the students conducting the study.
When questioned about potential regulatory actions, such as issuing a public alert, recalling affected vaccine batches, or notifying other agencies, the FDA stood firm in its defence of mRNA vaccine safety.
“If the FDA supplied the materials for the study and provided technical advice through staff supervision, then how can they not be responsible for the data?” @Kevin_McKernan asked. “Do they only deny their connection when the data becomes inconvenient?”
💥EXCLUSIVE: FDA lab uncovers excess DNA contamination in COVID-19 vaccines
Explosive revelations as a study conducted at FDA's own lab found residual DNA levels exceeded safety limits by 6 to 470 times. Experts say it's a 'smoking gun.'
@Kevin_McKernan @Jikkyleaksblog.maryannedemasi.com/p/exclusive-fd…
Nikolai Petrovsky, a Professor of Immunology and director of Vaxine Pty Ltd, described the findings as a “smoking gun.”
“It clearly shows the FDA was aware of these data. Given that these studies were conducted in their own labs under the supervision of their own scientists, it would be hard to argue they were unaware,” he said.
In addition to genome integration, @Kevin_McKernan highlighted another potential cancer-causing mechanism of DNA contamination in the vaccines.
Plasmid DNA fragments entering the cell's cytoplasm with the help of lipid nanoparticles, could overstimulate the cGAS-STING pathway, a crucial component of the innate immune response.
“Chronic activation of the cGAS-STING pathway could paradoxically fuel cancer growth,” McKernan warned.
But now, even the most entrenched vaccine proponents like Stanley Plotkin say that the @CDCgov schedule for immunising children is "too crowded."
The solution? Plotkin says we need "combination" vaccines - he believes fewer injections, means fewer adverse events.
🔥TGA ignored DNA fragments in Gardasil HPV vaccine
International drug regulators said there were DNA fragments in the Gardasil vaccine, but Australia’s regulator @TGAgovau sat on its hands and did nothing
It was known as early as 2003 that when DNA fragments bind to aluminium adjuvants (like AAHS), they undergo conformational change and can be introduced into the human cell via a process called “gene transfection.” researchgate.net/publication/24…
That means all recombinant vaccines (which have residual DNA fragments), when mixed with “transfection agents” such as aluminium adjuvants, polysorbates and lipid nanoparticles, have the potential for gene transfection.
Infanrix-Hexa® is a vaccine that lies at the heart of the Australian National immunisation program - administered to infants at 2, 4 & 6 months of age.
There are 43 reports of sudden infant deaths post-vaccination. @TGAgovau tries to kill the story by ignoring media enquiries.
Analysis of European docs found a "cluster" of sudden infant deaths after vaccination with Infanrix-Hexa®
Report concluded, “The clustering of deaths soon after immunisation suggests that the deaths were caused by the vaccine.”