Take out your thymus and, amongst other things, that's your immune tolerance broken, aka a trigger for multiple autoimmune disorders like lupus after a build up of usually 3+ years.
The role of thymic tolerance in CNS autoimmune disease
The thymus is one of the main sources for regulatory T cells and other cells to keep Th17 in check, which will also drive all sorts of immune dysregulation, now you add the Hematopoietic stem/Progenitor cells damage by the Spike alone and we have a very concerning trend going on.
There is more to it, but I need to do more research, and ask permission to divulge parts of the information because someone else cracked that one (person wishes to remain anonymous, same person who collaborated with me on the PAID hypothesis).
I've been looking into GP 120 & IL6 in some detail. You don't need GP 120 for the induced pathology but it helps.
I really hope spike protein is not as oncogenic as HIV. We will find out in the next 1-3 years.
This Substack explores the oncogenic potential of GP120, of how it upregulates cytokines including oncogenic interleukin 6, how both upregulate a multidrug resistant protein, the pathology of MRP1 and finally some potential therapeutics are explored.
Spike protein (inc vax) induced immunodeficiency & carcinogenesis megathread #27: Further investigations into GP120, IL-6 & multidrug resistance
Look up my post about Oncogenes. I don't think SARS 2 needs the GP120 to set off cancer. In my opinion the GP120 act as a molecular clamp, and for novel receptor use (novel in SARS). Will check your post later 😃
It doesn't need it, there are so many other pro-tumor pathways & immunosuppression to various degrees & durations we now know about as contenders. I guess P53 & BRCA must be near top of the list, along with cytokines, TLRs, RT, tumor suppressor antibodies etc but micro RNAs feature heavily on another level.
I was wondering the same thing about the thymus gland study, would that happen with just the spike protein? In any case, it seems this virus, if that's what it is, is wreaking havoc as well. Thanks for the article! 🙏💕
I gave a name months ago to what the virus inflicts. The everything disease. It has too many parts, of too many things. Look up Reverse AIDS part IV, it has a paper on the antigenic sites mimicry from a bunch of other pathogens. I didn't even get into the mimicry aspect that much (Plagued by Design II has some about it). Thank you 😊
The spike protein comes in TWO flavors: one is coded with Uracil, the other one is embedded with Pseudouridine (aka Pseudouracil). That is, the nucleobase Uracil has been replaced, in the cmRNA vaccines, with the nucleoside Pseudouridine (isomer of Uridine). This is actually a CRISPR-RNA level manipulation of the genetic code, which is known now to cause chromothripsis. No genotoxicity studies were done, no one supervised the chemist K. Kariko when she replaced Uracil with Pseudouridine, in what could be the most disastrous medical decision ever taken. The spike protein has other names: liquid crystal, T-bacilli, prion. Since the spike proteins are isomeric (in the cmRNA vaccines), the resulting antibodies will be isomeric as well (different configuration/chirality of the amino acid chains). Such isomeric binding abs can become neurotoxic in the split of a second, should the SUFFICIENT conditions arise.
Delta and Omicron are DIFFERENT pathogenic agents: Delta = M. avium (aka Sars-Cov-2), while Omicron = M. influenzae (aka Mers-Cov). The virulence of the Delta variant was caused by its prion domain. Prion = T-bacilli = absorption of aether which in turn causes severe hypoxia and micro blood clots (dextrorotatory prions). So far, Omicron's prion domain is inactivated. Omicron uses the DPP4 cellular receptor, same as Mers-Cov.
There might an intermediate stage between VOC and VOHC.
I try not to pay attention to the children stuff otherwise I will develop a ulcer and break my jaw from clenching it. The younger you Jab, the faster they react, the more probable long term issues become...
Take out your thymus and, amongst other things, that's your immune tolerance broken, aka a trigger for multiple autoimmune disorders like lupus after a build up of usually 3+ years.
The role of thymic tolerance in CNS autoimmune disease
Adam E Handel et al. Nat Rev Neurol. 2018 Dec.
https://pubmed.ncbi.nlm.nih.gov/30451970/
The thymus is one of the main sources for regulatory T cells and other cells to keep Th17 in check, which will also drive all sorts of immune dysregulation, now you add the Hematopoietic stem/Progenitor cells damage by the Spike alone and we have a very concerning trend going on.
There is more to it, but I need to do more research, and ask permission to divulge parts of the information because someone else cracked that one (person wishes to remain anonymous, same person who collaborated with me on the PAID hypothesis).
Another great piece in the puzzle thanks.
I've been looking into GP 120 & IL6 in some detail. You don't need GP 120 for the induced pathology but it helps.
I really hope spike protein is not as oncogenic as HIV. We will find out in the next 1-3 years.
This Substack explores the oncogenic potential of GP120, of how it upregulates cytokines including oncogenic interleukin 6, how both upregulate a multidrug resistant protein, the pathology of MRP1 and finally some potential therapeutics are explored.
Spike protein (inc vax) induced immunodeficiency & carcinogenesis megathread #27: Further investigations into GP120, IL-6 & multidrug resistance
https://doorlesscarp953.substack.com/p/spike-protein-inc-vax-induced-immunodeficiency-298?s=w
Look up my post about Oncogenes. I don't think SARS 2 needs the GP120 to set off cancer. In my opinion the GP120 act as a molecular clamp, and for novel receptor use (novel in SARS). Will check your post later 😃
It doesn't need it, there are so many other pro-tumor pathways & immunosuppression to various degrees & durations we now know about as contenders. I guess P53 & BRCA must be near top of the list, along with cytokines, TLRs, RT, tumor suppressor antibodies etc but micro RNAs feature heavily on another level.
I was wondering the same thing about the thymus gland study, would that happen with just the spike protein? In any case, it seems this virus, if that's what it is, is wreaking havoc as well. Thanks for the article! 🙏💕
I gave a name months ago to what the virus inflicts. The everything disease. It has too many parts, of too many things. Look up Reverse AIDS part IV, it has a paper on the antigenic sites mimicry from a bunch of other pathogens. I didn't even get into the mimicry aspect that much (Plagued by Design II has some about it). Thank you 😊
👍🏽
The spike protein comes in TWO flavors: one is coded with Uracil, the other one is embedded with Pseudouridine (aka Pseudouracil). That is, the nucleobase Uracil has been replaced, in the cmRNA vaccines, with the nucleoside Pseudouridine (isomer of Uridine). This is actually a CRISPR-RNA level manipulation of the genetic code, which is known now to cause chromothripsis. No genotoxicity studies were done, no one supervised the chemist K. Kariko when she replaced Uracil with Pseudouridine, in what could be the most disastrous medical decision ever taken. The spike protein has other names: liquid crystal, T-bacilli, prion. Since the spike proteins are isomeric (in the cmRNA vaccines), the resulting antibodies will be isomeric as well (different configuration/chirality of the amino acid chains). Such isomeric binding abs can become neurotoxic in the split of a second, should the SUFFICIENT conditions arise.
Thanks for this informative comment.
Delta and Omicron are DIFFERENT pathogenic agents: Delta = M. avium (aka Sars-Cov-2), while Omicron = M. influenzae (aka Mers-Cov). The virulence of the Delta variant was caused by its prion domain. Prion = T-bacilli = absorption of aether which in turn causes severe hypoxia and micro blood clots (dextrorotatory prions). So far, Omicron's prion domain is inactivated. Omicron uses the DPP4 cellular receptor, same as Mers-Cov.
There might an intermediate stage between VOC and VOHC.
VOHC = variant of high consequence
I try not to pay attention to the children stuff otherwise I will develop a ulcer and break my jaw from clenching it. The younger you Jab, the faster they react, the more probable long term issues become...