Unvetted ( by me. Will read) Bnabs each only block 90% of strains. May take multiple courses to cover the gap. #Cure4HIV #HIVCure
Unvetted ( by me. Will read) Bnabs each only block 90% of strains. May take multiple courses to cover the gap. #Cure4HIV #HIVCure
bsky.app/profile/sail...
Some caveats. One paper is showing success in "animal models" ugh. Not a big newc deal. We've been able to cure / prevent HIV in apes and humanized mice with bnabs since 2012! Generating them isn't enough. Maintaining them is despite multiple barriers.
Challenges: Generating high enough bnabs in humans is bigger problem. The animal models just aren't accurate. Bnabs are often targeted by the immune system ( anti antibodies) resulting in levels too low to work.
Or the immature lymphocytes needed for their creation, are culled in humans with a certain common HLA types to prevent autoimmune diseases.
There are humans study www.science.org/doi/10.1126/... But it's only stage 1 trial : which is done for safety& proof of concept! I'll be surprised if they've maintained neutralizing levels after 18 mos This might be a breakthrough; But may be a dead end we've reached before. Proof is in pudding
Background: Nobel nominate scientist David Baltimore cured HIV with bnabs in animal models ( humanized mice models and chimps ) using vectured vaccines ( which used muscle cells to turn out bnabs ) in 2012. They were unable to generate high enough levels in humans long-term.
This is a different technology. ( An even harder one to pull off ) ie the scientific achievement here in biotechnology Is still only that. And not an achievement in disease prevention or cure. That requires a high sustainability and replicatabily in a broad number of people that hasn't worked
I hope that stage one trials actually go somewhere. This could be quite a breakthrough.
I don't have an unlocked copy. But I don't think so. A significant percentage of people developed long-term hives. ( Not transient) They have no explanations why or ways to stop it.
Hives can be weird.