Anonymous ID: 75cd7f Dec. 15, 2021, 2:35 p.m. No.15198976   🗄️.is 🔗kun   >>9596

Back in July 2021, many scientists had the ill-founded view that the C-19 pandemic was dying out and entering an endemic state. Based on my understanding of the interplay between the virus and the immune system, I knew that this was not going to be the case and reacted immediately to this misinterpretation (https://www.voiceforscienceandsolidarity.org/scientific-blog/a-last-word-of-caution-to-all-those-pretending-the-covid-19-pandemic-is-toning-down). Once again, many scientists find themselves with the belief that the emergence of the Omicron variant announces the end of the pandemic and the virus’ transition into endemicity. Their prediction is largely based upon the initial observation that Omicron seems to be causing rather mild disease symptoms which they interpret as being indicative of a virus that—although more infectious—is now becoming less virulent and, therefore, increasingly featuring endemic behavior. I am afraid that once again, I don’t agree—a pandemic can only be tamed by herd immunity. Given the high vaccine coverage rates in most industrialized countries, we have generated anything but herd immunity. I also have yet to hear any compelling evidence concerning significant mutations in the genes that determine SARS-CoV-2’s virulence. Perhaps we should think twice before making statements that are not supported by immunological evidence.

 

 

This is what I believe is currently happening.

 

 

As Omicron appears largely resistant to neutralizing antibodies (Abs), it no longer strongly binds to vaccinal Abs (still directed at the spike protein [S] of the Wuhan strain). More specifically, Omicron allows for the restoring of full functional capacity of relevant innate Abs. The latter are known to be very efficient in preventing or abrogating productive infection and, therefore, preventing (severe) disease in individuals endowed with an intact innate immune system (i.e., people in good health and without underlying diseases or immune suppression, including vaccine-mediated immune suppression). As vaccinal neutralizing Abs are highly specific, they are less likely to bind to the receptor-binding domain (RBD) of Omicron, which has undergone a multitude of mutations within this very domain. It is, therefore, reasonable to expect that the vaccine-mediated Abs will fail to outcompete relevant innate Abs in vaccinees and hence, increase the incidence of asymptomatic infections in this population. It is intriguing that the Israeli Ministry of Health interprets asymptomatic infection in vaccinees as proof of “full protection” despite the fact that Omicron is highly suspicious of bypassing neutralizing antibodies (1, 2). Asymptomatic disease is known to lead to a short duration of anti-S Ab titers (3, 4). However, due to the high level of infectivity of Omicron, re-exposure to the virus is highly likely to occur with a timeframe that is short enough to coincide with elevated anti-S Ab levels. Consequently, dominant circulation of Omicron would ultimately make vaccinees more frequently susceptible to disease, whereas fewer and fewer unvaccinated individuals would be susceptible to contracting C-19 disease as a result of innate immune training upon viral exposure. In conclusion, it seems highly unlikely that dominant circulation of Omicron will result in diminished incidence of disease and cause the pandemic to transition into an endemic state. In contrast to the situation in the pre-Omicron era, the incidence of disease is now likely to disproportionately increase in vaccinees. This may, once again, prompt public health authorities to follow the erroneous advice of the vaccine industry and key opinion leaders who will undoubtedly recommend to continue the mass vaccination program using updated vaccines that suit the S version of the Omicron variant. In a previous contribution, I’d already predicted the dire consequences such a decision would entail (https://www.voiceforscienceandsolidarity.org/scientific-blog/mass-vaccination-will-push-sars-cov-2-spike-protein-beyond-omicron)—in brief, it will allow the virus to make a natural selection favoring hosts who preserved a fully functional innate immune defense.

 

https://www.voiceforscienceandsolidarity.org/scientific-blog/breakthrough-sars-cov-2-infections-are-a-pain …

Anonymous ID: 75cd7f Dec. 15, 2021, 2:51 p.m. No.15199037   🗄️.is 🔗kun   >>9046

COVID vaccination and age-stratified all-cause mortality risk… suggests the risks of COVID vaccines and boosters outweigh the benefits in children, young adults, and older adults with low occupational risk or previous coronavirus exposure

 

https://twitter.com/RWMaloneMD/status/1470953264095113217

Anonymous ID: 75cd7f Dec. 15, 2021, 2:53 p.m. No.15199046   🗄️.is 🔗kun

>>15199037

Accurate estimates of COVID vaccine-induced severe adverse event and death rates are critical for risk-benefit ratio analyses of vaccination and boosters against SARS-CoV-2 coronavirus in different age groups. However, existing surveillance studies are not designed to reliably estimate life-threatening event or vaccine-induced fatality rates (VFR). Here, regional variation in vaccination rates was used to predict all-cause mortality and non-COVID deaths in subsequent time periods using two independent, publicly available datasets from the US and Europe (month-and week-level resolutions, respectively). Vaccination correlated negatively with mortality 6-20 weeks post-injection, while vaccination predicted all-cause mortality 0-5 weeks post-injection in almost all age groups and with an age-related temporal pattern consistent with the US vaccine rollout. Results from fitted regression slopes (p<0.05 FDR corrected) suggest a US national average VFR of 0.04% and higher VFR with age (VFR=0.004% in ages 0-17 increasing to 0.06% in ages >75 years), and 146K to 187K vaccine-associated US deaths between February and August, 2021. Notably, adult vaccination increased ulterior mortality of unvaccinated young (<18, US; <15, Europe). Comparing our estimate with the CDC-reported VFR (0.002%) suggests VAERS deaths are underreported by a factor of 20, consistent with known VAERS under-ascertainment bias. Comparing our age-stratified VFRs with published age-stratified coronavirus infection fatality rates (IFR) suggests the risks of COVID vaccines and boosters outweigh the benefits in children, young adults and older adults with low occupational risk or previous coronavirus exposure. We discuss implications for public health policies related to boosters, school and workplace mandates, and the urgent need to identify, develop and disseminate diagnostics and treatments for life-altering vaccine injuries.

 

https://www.researchgate.net/publication/355581860_COVID_vaccination_and_age-stratified_all-cause_mortality_risk

 

should make notables if not already included in previous breads