I said it from the start: Coronavirus vaccines don’t work for the ones who would need them the most because a functioning immune system is needed to make it work <— That’s the irony of this stupidity they have been trying to sell us.
We encounter endless amounts of pathogens daily. A healthy and fully functioning immune system can handle pathogens as it always has for millions of years.
"In addition, BNT162b2 is nucleoside-modified by a substitution of 1-methyl-pseudouridine for uridine and thus its inherent adjuvant activity mediated by binding to innate immune sensors such as toll-like receptors (TLRs) 7 and 8, is dampened, but not abrogated."
Have you seen this Manu? It speaks to a muted T-cell response as a result of the formation of "non-inflammatory" IgG4 antibodies, especially in the time post 3rd or booster vax;
There is a link to the root preprint in this post. I believe it to be a key puzzle piece in understanding how these shots are negatively affecting our immune function.
Multiple signs that the repeated injections are having a detrimental affect on the immune system. At least in relation to sars-cov-2 infections. What is their next play? Coming into fall, are we going to see another big push to get your 4th/5th booster for the new variant? Whatever problems exist with the vaccine should become more and more pronounced as people get more doses.
I said it from the start: Coronavirus vaccines don’t work for the ones who would need them the most because a functioning immune system is needed to make it work <— That’s the irony of this stupidity they have been trying to sell us.
We encounter endless amounts of pathogens daily. A healthy and fully functioning immune system can handle pathogens as it always has for millions of years.
—> mutation rates of coronaviruses
—> health risk benefit / side effects
—> negative efficacy
END OF STORY ! ❤️
I suspect it may in part be due to "dampened" TLR 7 & 8 responses, necessary to activate the T cell.
TLR7 [62, 63] Endosome ssRNA viruses (vesicular stomatitis virus, influenza virus)
TLR8 [64–66] Endosome ssRNA from RNA viruses
https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7726878/
"In addition, BNT162b2 is nucleoside-modified by a substitution of 1-methyl-pseudouridine for uridine and thus its inherent adjuvant activity mediated by binding to innate immune sensors such as toll-like receptors (TLRs) 7 and 8, is dampened, but not abrogated."
https://www.ema.europa.eu/en/documents/assessment-report/comirnaty-epar-public-assessment-report_en.pdf
comirnaty-epar-public-assessment-report_en.pdf
Have you seen this Manu? It speaks to a muted T-cell response as a result of the formation of "non-inflammatory" IgG4 antibodies, especially in the time post 3rd or booster vax;
https://unglossed.substack.com/p/boosting-tolerance-igg4
There is a link to the root preprint in this post. I believe it to be a key puzzle piece in understanding how these shots are negatively affecting our immune function.
Multiple signs that the repeated injections are having a detrimental affect on the immune system. At least in relation to sars-cov-2 infections. What is their next play? Coming into fall, are we going to see another big push to get your 4th/5th booster for the new variant? Whatever problems exist with the vaccine should become more and more pronounced as people get more doses.
Interesting stuff, Manu!
I am sure many people could be found to take part in gene editing trials —> One would simply have to ask them.