Turner et al.: "SARS-CoV-2 infection induces long-lived bone marrow plasma cells in humans"; yes, one year ago published but swept under the rug by CDC, NIH, FDA, media as if it did NOT exist
This paper showed us what we needed to know as to long-lived immunity with COVID virus yet it was as if it was never published so I re-highlight; why? because natural immunity is life-long!
Well, as an example, we knew that long-lived bone marrow plasma cells (BMPCs) provided robust protection. We always knew this (see 1,2,3,4,5,6,7). We also knew that once COVID-recovered, you were at significantly lower risk of re-infection with COVID virus and that the virus had to be appreciably different (substantially mutated on the target antigen) to breach immunity (see 8,9,10). Omicron is highly infection (e.g. BA.4 and BA.5 clades) and presents as a nearly different (sufficiently different) virus given the multiple mutations on the spike protein to present the immune system with a rechallenge and a potential breach. However, the predominant symptoms are mild akin to a common cold.
What did Turner et al. show in the NATURE publication?
SOURCE:
SARS-CoV-2 infection induces long-lived bone marrow plasma cells in humans
‘Here we show that in convalescent individuals who had experienced mild SARS-CoV-2 infections (n = 77), levels of serum anti-SARS-CoV-2 spike protein (S) antibodies declined rapidly in the first 4 months after infection and then more gradually over the following 7 months, remaining detectable at least 11 months after infection. Anti-S antibody titres correlated with the frequency of S-specific plasma cells in bone marrow aspirates from 18 individuals who had recovered from COVID-19 at 7 to 8 months after infection. S-specific BMPCs were not detected in aspirates from 11 healthy individuals with no history of SARS-CoV-2 infection.
We show that S-binding BMPCs are quiescent, which suggests that they are part of a stable compartment. Consistently, circulating resting memory B cells directed against SARS-CoV-2 S were detected in the convalescent individuals. Overall, our results indicate that mild infection with SARS-CoV-2 induces robust antigen-specific, long-lived humoral immune memory in humans.’
Turner et al.: "SARS-CoV-2 infection induces long-lived bone marrow plasma cells in humans"; yes, one year ago published but swept under the rug by CDC, NIH, FDA, media as if it did NOT exist
Mrs S: By having 'had COVID' three times, do you mean you have had three separate bouts of acute infectious respiratory disease or simply had three positive PCR tests?
Please bear in mind that PCR is not a diagnostic test for disease. Further, the WHO's protocol gives rise to a false-positive rate in excess of 97%, which makes testing meaningless. Therefore, there is no way of identifying the infectious agent involved by PCR.
Kind regards.
In the individual case of MrsS, her assumptions may or may not be correct. Certainly everything Spradbery points out is certainly otherwise correct. Those are the facts.
Among the other facts, the supposed "variants" are a product of a well-known process of biological adaptation called Natural Selection; i.e., natural forcings trigger adaptation in a manner that "selects-for" the more enduring adaptations.
If MrsS is indeed a victim of subsequent "covid variants" then she is a victim of experimental "covid vaccine" inoculation policy. The most dominant influential forcings of adaptive covid variation is the obscene and willfully reckless policy of mass inoculation using suboptimal "vaccines" that MUST select-for resistance and greater virulence by the fact of their sub-optimality and ineffectiveness.
If MrsS had a bacterial infection and she continued to practice the ingestion of antibiotics that were sub optimal and mostly ineffective, what would happen? Her practice would select-for resistant strains of bacteria.
What would happen if 60% of every person on the planet were subject to the same practice of selecting for a bacteria that the body could no longer control or kill off? We would eventually select for a resistant bacterial strain the body could not endure and mass die-offs (another selection event) in the subject human populations would result.
Like what happened to the lady who accidentally backed into the airplane propeller: disaster.
You only have to take spike protein once. The genetic alteration created by spike begins a new mRNA process that on a nano-level creates the repeated amplification of "spike protein dosing" by the ordinary mechanism native to mRNA activity in the human body. The more inoculations with spike, the worse and more intensive the forcings will become.
The MrsS wellness conundrum may be as simple as pernicious malnutrition. If she has slipped into sub-clinical hypoascorbemia, her body cannot heal as it otherwise could should that deficit corrected and the correction sustained.
My apologies for the meandering comment, but MrsS seemed to be genuinely curious and she needs to contemplate greater issues. Why? A virus is not a bacteria.
In every discernible way, a virus is not a bacteria. That's the first deception the orthodoxy exploits to confuse good people into becoming willing victims of an unconscionably perverse and dangerous mass human experiment with experimental technology being used in humans for the very first time on a mass scale without the standard controls and regulatory protections that are required for every other form of medical chemical or substance they sanitize with the terms "drug" and "vaccine."
It's not the sickness but the healing that matters most.
"Among all things, first do no harm."
That central unifiying principle competes with another popular central unifying principle.
"Among all things, first get the money."
Our mutual lives and livelihoods hang in the balance as do lives of all of those we each know and love.