Anyone know why administering IGg3 antibodies is a bad idea as they would NOT sterilize spike protein infections via the SARS-COV2 virus or via C19 mRNA injections?
A week ago I posted this article:
Before I get irretrievably lost down this particular rabbit hole, I thought I would post some more background on IGg3.
From here:
“Immunoglobulin IgG3 is one of the four subclasses IgG1 to IgG4 that make up the human IgG antibodies. It is the third most abundant IgG in serum and comprises 5% to 8% of serum IgG. IgG3 plays a role in protection against intracellular bacteria, parasites, and viruses. IgG3 is unique in the four subclasses, as it is the only subclass that has not as yet been exploited as a biotherapeutic.”
here:
Molecular IgG3 structure paves the way for new applications of antibodies - - Diamond Light Source
“In work recently published in the Journal of Biological Chemistry, researchers from University College London and the University of Birmingham have used a combination of imaging and analytical methods to provide the first experimentally determined molecular structural model for a full-length IgG3 antibody. This new information should enable the use of IgG3 to develop new therapies and antibody tests.”
You can get IgG3 Fc Region Recombinant Protein Lyophilized here (some human and mostly mouse!).
IGg3 - Innovative Research (innov-research.com)
All clues and research suitable for a layman welcome!
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Not related, but just saw Karen Kingston's attack on Sasha Latypova whom she considers "latest expert psyop protecting Pfizer from liability".
Rintrah Radagast published a definitive article that explains this in layman’s terms: https://www.rintrah.nl/the-trainwreck-of-all-trainwrecks-billions-of-people-stuck-with-a-broken-immune-response/