Saturday, January 15, 2022

major missing piece in Sars2/vax puzle surfaces

 many of those injected with the so-called “vaccine” are having thei immune systems wiped out and they’re exhibiting rare symptoms that are commonly seen in AIDS patients….K Kingston then gets into the evidence of how the vaccine produces the spike protein that contains HIV GP120, which could explain why these unusual symptoms are happening.
She says “The codon, the sequence for HIV glycoprotein 120 is in the spike protein.  It’s called ‘double CGG’…
“And what’s more alarming is…one study was done in 2004  (study shown below)—by these authors:
    Moore MJ, Harvard Medical /Partners AIDS Research Center, Brigham and Women's Hospital, Department of Medicine (Microbiology and Molecular Genetics), Boston
    Dorfman T,
Li W, Wong SK, Li Y, Kuhn JH,    

Jens H. Kuhn - Principal - Tunnell Government Services, Inc.
        Principal Scientist and Director of Virology (NIH/NIAID/DCR/Integrated Research Facility at Fort Detrick)
https://www.linkedin.com › jens-h-kuhn-0728171b  

Jens H Kuhn. Division of Therapeutic Proteins, Office of Biotechnology Products, NIH/NIAID  kuhnjens@niaid.nih.gov
 

James Coderre, University of Massachusetts Medical School  Genetics and Genomics | Molecular Biology | Molecular Genetics
Vasilieva N, Han Z, Greenough TC,
M. Farzan, Co-Chair, Immunology and Microbiology , Scripps Research 


  Retroviruses pseudotyped with the severe acute respiratory syndrome coronavirus spike protein efficiently infect cells expressing angiotensin-converting enzyme 2
Michael J Moore  1 , Tatyana Dorfman, Wenhui Li, Swee Kee Wong, Yanhan Li, Jens H Kuhn, James Coderre, Natalya Vasilieva, Zhongchao Han, Thomas C Greenough, Michael Farzan, Hyeryun Choe
Affiliations   
Affiliations
    •    PMID: 15367630
    •    PMCID: PMC516384
    •    DOI: 10.1128/JVI.78.19.10628-10635.2004

  Infection of receptor-bearing cells by coronaviruses is mediated by their spike (S) proteins.  The coronavirus (SARS-CoV) that causes severe acute respiratory syndrome (SARS) infects cells expressing the receptor angiotensin-converting enzyme 2 (ACE2). Here we show that codon optimization of the SARS-CoV S-protein gene substantially enhanced S-protein expression. We also found that two retroviruses, simian immunodeficiency virus (SIV) and murine leukemia virus, both expressing green fluorescent protein and pseudotyped with SARS-CoV S protein or S-protein variants, efficiently infected HEK293T cells stably expressing ACE2. Infection mediated by an S-protein variant whose cytoplasmic domain had been truncated and altered to include a fragment of the cytoplasmic tail of the human immunodeficiency virus type 1 envelope glycoprotein was, in both cases, substantially more efficient than that mediated by wild-type S protein.  Using S-protein-pseudotyped SIV, we found that the enzymatic activity of ACE2 made no contribution to S-protein-mediated infection.  Finally, we show that a soluble and catalytically inactive form of ACE2 potently blocked infection by S-protein-pseudotyped retrovirus and by SARS-CoV. These results permit studies of SARS-CoV entry inhibitors without the use of live virus and suggest a candidate therapy for SARS.

FIG. 1.
Efficient expression of codon-optimized S…

https://pubmed.ncbi.nlm.nih.gov/15367630/
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(similar article)
11-27-03
 (SARS), associate with cellular receptors to mediate infection of their target cells. Here we identify a metallopeptidase, angiotensin-converting enzyme 2 (ACE2), isolated from SARS coronavirus (SARS-CoV)-permissive Vero E6 cells, that efficiently binds the S1 domain of the SARS-CoV S protein.  We found that a soluble form of ACE2, but not of the related enzyme ACE1, blocked association of the S1 domain with Vero E6 cells. 293T cells transfected with ACE2, but not those transfected with human immunodeficiency virus-1 receptors, formed multinucleated syncytia with cells expressing S protein. Furthermore, SARS-CoV replicated efficiently on ACE2-transfected but not mock-transfected 293T cells. Finally, anti-ACE2 but not anti-ACE1 antibody blocked viral replication on Vero E6 cells. Together our data indicate that ACE2 is a functional receptor for SARS-CoV.
    •    
     Li W, Moore MJ, Vasilieva N, Sui J, Wong SK, Berne MA, Somasundaran M, Sullivan JL, Luzuriaga K, Greenough TC, Choe H, Farzan M. Nature. 2003 Nov 27;426(6965):450-4. doi: 10.1038/nature02145. PMID: 14647384
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12-21-21
“So by adding HIV glycoprotein 120 they made it more receptive to the ACE-2 receptors in your lungs and kidneys as well as to your T cells, your CD4 cells, to annihilate them.
“Now this is the part where people’s jaws are going to drop:  We know CGG is not found in nature, therefore it’s patentable.  Well, who did all the research on this? And who owns it?  Well, Dr Fauci did a number of studies, he paid himself over $11.677 million with US taxpayer dollars, between 2014 and 2020 to research, using glycoprotein 120 from HIV and integrating it into coronaviruses – and he patented it.  He owns several patents on this.
“So every time someone’s being injected with the synthetic mRNA, producing the Wuhan-HU-1 spike glycoprotein, Fauci is making a dime…
“This isn’t a matter of interrogating Dr Fauci.  The evidence is there that this man is a global genocidal sociopath and he’s caused the death of millions of American adults and children and he’s also induced autoimmune disease.
“Keep in mind, RNA, the coronavirus, whether it was synthetically-made or whether it was zoonotic or human-infected, it’s an unstable virus.  Children never get infected.
“What the scientists did, in collaboration with Dr Fauci is they took an unstable virus, encapsulated it into a biosphere, added chimeric gain-of-function weaponization of this virus, injected it into human bodies and told them this was ‘safe and effective’.
“Meanwhile a child who would have no chance of ever getting infected with this is now injected with a bioweapon, it hijacks their perfectly healthy, balanced, in-order immune so that they actually produce a disease-causing spike glycoprotein and wipes out their immune system, so they develop autoimmune disease, also known as Acquired Immuno Deficiency Syndrome, also known as AIDS…
“This is nothing short of conspiring to commit aggravated assault and murder of children (and others).  That is all it is…
“We’re going to see an onslaught of rare auto-immune diseases, just like we saw with HIV, just things that people had never seen.  Adults were coming down with cat leukemia, they were coming down, again with something called MAC, which is caused by earthworm excrement.  They also had major neurological disorders.  This is what we’re bringing onto the American people and onto our children.”
Kingston believes that the doctors who are going along with this are financially motivated and that Anthony Fauci and the legions of his accessories belong in jail.”

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