Posted on 01/12/2022 5:47:53 AM PST by Red Badger
” What that means is it took 293 … living babies that were born.”
So much lying ...
They don’t do much. I had a full course of convalescent plasma therapy. Along with remdesivir and lots of steroids. The doctors say I was near death. They didn’t expect me to live.
But I held on. Maybe these treatments helped a little. Maybe they didn’t. For me, by the time I got to the hospital, the virus had already made me very ill, and the virus was already declining. It’d done its damage, but my own immune system (which is suppressed by medication) was already defeating the virus. But the question was, would I survive the damage? Obviously, I did. But it took 25 days in the hospital of my ow body slowly healing, slowly ridding me of the ‘rona pneumonia.
So, did the convalescent plasma therapy help? Or any of the other treatments? Maybe a little. But no dramatic effect.
They didn’t humanize the mice. It’s a chimera.
293 isn’t number of fetuses. It’s the number of the experiment.
My sources tell me this isn’t a very compelling argument.
I got the antibody cocktail under duress; it was that, or go to the hospital. I had no idea they had the fruit of an evil tree (ABORTION) in them. And now, it CANNOT EVER be removed from our bodies. I pray the Lord Jesus will forgive me. It is just another sin among many.
Pray for those of us who took them under duress and in ignorance.
“
Essentially the entire human Ig heavy and kappa light chain variable repertoire has been integrated into ES cells. The resulting genomic loci are stable throughout multiple generations of VelocImmune mice and have been shown to be used productively, generating antibodies of diverse fully-human variable sequences. Direct comparisons between VelocImmune mice and wild-type littermates demonstrate nearly identical responses to immunisation, regardless of the number of human variable segments the VelocImmune mice possess. High affinity therapeutic antibodies have been generated to many different antigens utilising standard hybridoma and cloning techniques, further highlighting the speed and efficiency of VelocImmune technology.
Despite the fact that the antibodies produced by VelocImmune mice possess mouse constant regions, Regeneron scientists have developed high-throughput methods for the joining of desired variable regions to human constant regions of any type, and the subsequent insertion into mammalian production lines to create fully-human antibodies. Because of the modular nature of antibody variable domains, specificity and affinity are maintained whether on mouse or human constant regions. Thus, the advantage of producing antibodies in vivo possessing human variable regions joined to mouse constant regions does not create any problem for the creation of fully-human antibody therapeutics.
Regeneron has used VelocImmune technology to create a broad pipeline of antibody therapeutics to a variety of targets. REGN88, directed against human interleukin 6 (IL6) receptor, is Regeneron’s first fully-human antibody in clinical trials for the treatment of rheumatoid arthritis.”
https://www.pharmafocusasia.com/clinical-trials/human-antibody-discovery
________
” VelocImmune
“Regeneron’s VelocImmune technology offers the potential to increase dramatically the speed and efficiency of discovering fully-human, therapeutic monoclonal antibodies. The VelocImmune platform generates fully human monoclonal antibodies (hMAbs) to address clinically relevant targets of therapeutic interest. The VelocImmune mouse, unlike other hMAb mice, mounts a robust immune response that is virtually indistinguishable from that of a wild type mouse, resulting in a reliable and efficient platform for discovering fully human monoclonal antibodies.”
_______
We show that these mice, termed VelocImmune mice because they were generated using VelociGene technology, efficiently produce human:mouse hybrid antibodies (that are rapidly convertible to fully human antibodies) and have fully functional humoral immune systems indistinguishable from those of WT mice. The efficiency of the VelocImmune approach is confirmed by the rapid progression of 10 different fully human antibodies into human clinical trials.
https://pubmed.ncbi.nlm.nih.gov/24706856/
So glad you’re ok now!
God’s grace is infinite....................
Not quite. I survived the ro, but I have a few other problems. If you could, pray for me. Thank you.
Can I still claim to be “pure blood” with these antibodies in my system?
What’s the consensus?
Go look up “induced pluripotent stem cells”...
A lot of what she said I have heard elsewhere.
However……..
Mr. mm and I listened to the podcast, and she is way put there on a few issues.
Whatever she claims should be evaluated in light of other sources.
And repeat all that testing from aborted cells. Hell. They know exactly how HEK 293 or the others will respond to my piss. Why retest all that just to be ethical. FU you aborted baby loving Vax mandate troll.
That is easy as can be. They do not want to re run all the tests (over 30 years) against a ethical cell line. Umbilical stem cells are the future but the have invested so much $$$$ in abortion lines they can’t convince themselves to change. $>ethics and truth.
BTTT
Thanks.
Bkmk
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