mRNA COVID Vaccines Contain DNA That May Turn Human Cells Into Long-Term Spike Protein Factories, INDEFINITE; is it ok to ask what did Malone know & why did he not tell us? Is it ok? Should we ask?
by Paul Alexander
I have repeatedly asked him to be interviewed by me but no reply; we were colleagues & I am hoping he understands my role as an investigative reporter too as we seek answers; I am not ONLY a scientist
Spike produced for the rest of your life.
Huge report by Daily Skeptic, huge.
I do not find this surprising since we already know that vaccine mRNA can be reversed transcribed back to DNA in cells, human cells:
‘Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure.’
I want answers like you and I am tired of Malone talking about everything but the key issues around mRNA and the bioweapon. I am. I am not one of the money whores in the Freedom movement running around trying to figure out who to leech off of next.
I want Malone and anyone linked to the lockdown lunacy and the fraud gene injection platform to answer real questions, nothing scripted and no pink puff piece by our ‘friendly’ media people who are nothing more than money sucking leeches, pimping off the COVID pains. I know most. I work with them, it is not media now, in the Freedom movement, its a ‘friends’ game. We can no longer blame legacy media for we are like legacy media. We became legacy media.
Malone (and all like him, all linked to the vaccine in ANY manner, at any stage) should be hauled into congress with all others and those linked to the response and vaccine to find out how it was done, what was done, all issues on the harms, what was his role, anything he can share, not about the billions in contracts you got (if that is even true too) and how he can help fix the spike that is being produced literally 24/7 potentially for the rest of your life. The vaccinated are in serious trouble. He said he invented it, the mRNA technology, and that is at the heart of these shots. Kariko his colleague said bullshit, he did not, who knows, who is right? she seems credible and he threatened her by her accounts in her candid responses to Atlantic interview. I found troubling. I do not know what the hell to believe anymore for this is like a game. The inventor of the core technology is a celebrity and no one is asking him questions and he is not in front of congress not asked questions by congress members who know zip on this, but by proper scientists and people like me asked for questions like how they usually ask me.
I want to be fair to Malone and have an interview for he must answer questions and all those blocking for him must cease.
Daily Skeptic (Will Jones is a giant as usual in this piece, a hot tip is in order).
What did Malone know about this? What was his role in Remdesivir?
‘The mRNA Covid vaccines from Pfizer and Moderna contain billions of particles of self-replicating DNA that may turn human cells into long-term factories for the COVID-19 spike protein, a study has found.
The result is thought to shed light on the persistence of vaccine spike protein and mRNA in the body for months following inoculation, a worrying phenomenon which has not so far been fully explained – though earlier experiments also found evidence the vaccine mRNA may be reverse-transcribed into the cell DNA.
Persistence of spike protein is believed by experts to be a contributor to adverse effects of the COVID-19 vaccines by inducing auto-immune attacks on the heart and other organs, among other mechanisms.
The researchers found that the vaccines were contaminated with significant quantities of biological agents known as plasmids. Plasmids are small circular DNA molecules that can replicate in bacteria, including bacteria found inside humans – and also in human cells when the plasmids are suitably modified to be used as a genetic engineering or gene expression vehicle, as in this case. The plasmids found in the mRNA shots contain the DNA that codes for the mRNA that produces the spike protein. A cell that has taken in these plasmids may be able to produce the spike protein indefinitely.
The Moderna vaccine was found to contain one plasmid per 3,000 mRNA molecules while the contamination in the Pfizer vaccine was 10 times higher at one plasmid per 350 mRNA molecules. The ‘safe’ level for such double-stranded DNA contaminants is set by the European Medicines Agency as the equivalent of one part per 3,000 mRNA molecules – though the researchers note that it’s “not clear how they set these standards” or whether they “had considered contaminating DNA that was capable of amplifying inside the host”.
Moderna meets this ‘safe’ threshold but Pfizer is over it by a factor of 10. The researchers add that in either case it “equates to billions of antibiotic resistant plasmids injected per person per shot”. That’s before they replicate: “Billions of these contaminants per injection is likely an underestimate of the entire burden as these plasmids can self-replicate in bacterial hosts.”
The researchers express concern that the plasmids also confer resistance to the antibiotics neomycin and kanamycin on any bacteria that take them up, and worry that this may “transform the gut microbiome” of a human host.
The spike-manufacturing plasmids are an integral part of the vaccine manufacturing process, providing the blueprint for the mRNA, but why they continue to contaminate the vaccines at such high levels and have not been more fully removed is unclear.
Dr. Anthony Brookes, Professor of Genomics and Health Data Science at the University of Leicester, told the Daily Sceptic: “This is a solid piece of research by a very knowledgeable team.”
The DNA vector molecules from which the mRNA is created (‘transcribed’) is a stable entity, and it is shown to be present at non-trivial levels in the vaccines. It will therefore presumably get into bacteria and human cells throughout the injected person, to be potentially transcribed into mRNA and cause long-term expression of spike protein.
We must hope that vector-carrying, spike-expressing cells are progressively eliminated by the immune system, but if tolerance is created by long-term exposure to the toxic spike protein then this removal may not be very efficient. In this worst-case but feasible scenario, a residue of spike producing cells may exist for months or years – slowly and steadily damaging many organs and tissues in the vaccinated individual. Treatments that help to eliminate or negate the action of the spike protein need to be established, and fortunately various candidate interventions are now being reported.
Governments that have approved and mandated these products should make a priority of replicating these worrying findings and fully investigating their implications.’