Posted on 08/18/2021 4:01:33 PM PDT by NoLibZone
Those who take the Covid-19 “vaccines” are MORE susceptible to the Delta Variant and have a HIGHER risk of severe disease or even death. This information comes from Dr. Robert Malone, the inventor of the very mRNA technology used to transmit both the Pfizer and Moderna injections.
Malone took to Twitter to post a thread that has shockingly not been taken down yet. Twitter has been censoring posts that speak ill of the “vaccines,” and a high-profile physician and researcher like Dr. Malone seems ripe for censorship. Perhaps they fear the “Streisand Effect” with this particular thread and are simply suppressing it on the back end.
Same argument used for the "consensus" about "global warming."
The mRNA technology that didn’t prevent 100% of test animals from dying?
A million? Really?
LOL....
Your vaxx shill skills are strong today. Reply #4 on a Covid thread.
Keep on shillin'!
Does it pay well?
What does he know? He got banned on Youtube. We need to hear from the real expert. Holy Dr. Fauchi >s
“better risk of dying”
is what you’re driving at?
“ And what are your credentials?”
*************************************
Well, apparently unlike the illustrious Dr Malone, I’ve had the benefit of reading the Mayo Clinic study that compared the outcomes of three well-matched large cohorts - 1) unvaccinated 2) Moderna vaccinated and 3) Pfizer vaccinated. And, contrary to Dr Malone’s belief that it’s “Easier for Delta to Kill ‘Vaccinated’ than Jab Free People”, it wasn’t the vaccinated who were being hospitalized/dying — IT WAS THE UNVACCINATED. Surprise, surprise, surprise… NOT!
So anti-Vaxxers can continue to have their wet dreams of ADE arriving to smite those who got COVID-19 shots… but IT’S NOT A REALITY.
Of course it is. That’s standard issue anti-vax blog deception.
Not even Malone would go against the irrefutable data we have on hospitalizations and deaths among the unvaccinated vs. vaccinated.
You are correct. The data shows the opposite. He has gone quack.
He kneels before FauXi.
It appears to be a leaky vaccine. It is AED. All over the world except US media it is reported that it is the vaccinated getting sick.
Here is an article from the nih.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516275/
which talks about this
https://www.pbs.org/newshour/science/tthis-chicken-vaccine-makes-virus-dangerous
thanks
Not if no one reports it. I am seeing comments from people that have had serious problems like strokes at 40 and when they ask their doctor if it could be from the JAB, all they are getting as a response is a blank stare and no comment. That tells me no one is going to report it.
Mayo Clinic is probably bought and paid for just like the CDC by big Pharma and China.
A million what?
Everyone has opinions. Yours is as meaningless as the rest of us and much less than many of the people you denigrate.
Vaccine hesitancy has nothing to do with being anti vaccine. So say such is absolute nonsense and meant only to degrade the discussion.
Nobody wants to see ADE either, but its within the realm of possible.
Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan/D614G strain and Delta variants. A potential risk for mass vaccination
https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltext
Abstract
Antibody dependent enhancement (ADE) of infection is a safety concern for vaccine strategies. In a recent publication, Li et al. (Cell 184 :4203–4219, 2021) have reported that infection-enhancing antibodies directed against the N-terminal domain (NTD) of the SARS-CoV-2 spike protein facilitate virus infection in vitro, but not in vivo. However, this study was performed with the original Wuhan/D614G strain. Since the Covid-19 pandemic is now dominated with Delta variants, we analyzed the interaction of facilitating antibodies with the NTD of these variants. Using molecular modeling approaches, we show that enhancing antibodies have a higher affinity for Delta variants than for Wuhan/D614G NTDs. We show that enhancing antibodies reinforce the binding of the spike trimer to the host cell membrane by clamping the NTD to lipid raft microdomains. This stabilizing mechanism may facilitate the conformational change that induces the demasking of the receptor binding domain. As the NTD is also targeted by neutralizing antibodies, our data suggest that the balance between neutralizing and facilitating antibodies in vaccinated individuals is in favor of neutralization for the original Wuhan/D614G strain. However, in the case of the Delta variant, neutralizing antibodies have a decreased affinity for the spike protein, whereas facilitating antibodies display a strikingly increased affinity. Thus, ADE may be a concern for people receiving vaccines based on the original Wuhan strain spike sequence (either mRNA or viral vectors). Under these circumstances, second generation vaccines with spike protein formulations lacking structurally-conserved ADE-related epitopes should be considered.
The aim of the present study was to evaluate the recognition of SARS-CoV-2 Delta variants by infection enhancing antibodies directed against the NTD. The antibody studied is 1052 (pdb file #7LAB) which has been isolated from a symptomatic Covid-19 patient1. Molecular modeling simulations were performed as previously described2. Two currently circulating Delta variants were investigated, with the following mutational patterns in the NTD :
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