Posted on 01/12/2022 5:47:53 AM PST by Red Badger
It's been the "silver bullet" that so many have embraced. But what do we really know about monoclonal antibodies? Are they really better than the vaccines or are they just another experiment that's bound to go awry?
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There’s an odd disconnect among many who are opposed to the Covid-19 “vaccines.” We generally pan the experimental drugs for a wide variety of reasons ranging from the clear health risks and lack of efficacy all the way to many conspiracy theories that the jabs are just tools for depopulation. Some are opposed for religious reasons. Others are opposed out of pure distrust of Big Pharma and their lap dogs in government.
Whatever the reason someone has for being a “vaccine skeptic,” there are many who then go and embrace the monoclonal antibodies being offered as a safe and effective treatment for Covid-19. This is where the disconnect comes into play because many of the characteristics that make people skeptical of the vaccines are present in the “safe and effective” monoclonal antibodies.
On the latest episode of The Midnight Sentinel, I was joined by Dr. Carrie Madej. It was actually quite challenging to isolate an individual topic to highlight in this article because she drops multiple bombshells in the hour-long interview. I chose the monoclonal antibodies topic because it may be the most pressing for those who are currently experiencing or may soon be experiencing the rapidly spreading Omicron variant.
“Even in the freedom movement, the ‘anti-vaxxers,’ people are against getting these injections or genetic modification devices, really, but then I see those same people run to get the monoclonal antibodies and I think, ‘Oh, you just have no idea,'” she said.
“First of all, they’re brand new, they’re experimental, they have very little research on them, okay,” she continued. “You’re putting something in your body that we don’t have research on. However, we know something about it.
“So, these are called a cocktail. So, what that is, they’re taking antibodies from three sources. One is just a ‘human source.’ What does that mean? Is it somebody from the street? I mean, what is that? Do we know if they’re purified? We don’t know. Okay, that’s one.
“Number two, they’re using aborted fetal cells. When they say they’re not, they’re lying. They’re using a play on words. They’re using the HEK line, the human embryotic kidney cell line. It’s 293. What that means is it took 293 … living babies that were born. So they aborted them alive. They’re still living with their heart beating. Then they take them to a cold lab and then they kill them there.
“It took 293 of them to get that cell line. So what they do is they make those lines cancerous so they never stop dividing. They don’t want to tell you they’re putting cancer cells from an aborted fetus in you so they’re going to tell you that it’s ‘immortalized’ — isn’t that a nice word. Then they tell you they’re cloned. That’s what it means. You’re taking in an aborted fetus that was killed in a lab and then you had a cancerous cell line from it that’s being injected inside of you. Okay, so you’ve got two sources.
“Now, the third one is from a human and a mouse genome pushed together inside of a mouse, and the mouse spits out a human kind of an antibody but from a mouse. So this is something called a chimera. A chimera is two creatures pushed together and they’re going to be spitting out an antibody.
“Now, you have to understand, all the genetic material that a human body takes up, whether we eat it, whether we inhale it, we become injected with it… our bodies are amazing. It takes up genetic material to analyze it, sometimes incorporate it inside our genome. It’s called epigenetics.”
Even at this point of the interview, I was having concerns about the monoclonal antibodies based on the information I was hearing. But it was during the next portion of Dr. Madej’s answer that I became truly shocked.
“There’s a problem also with the human-mouse antibody cell line,” she continued. “It has a trade name called VelocImmune. So, I knew this, I recognized this from years ago when I had a very big practice here in Georgia. I took different cases, complicated, and of course I got cancer patients. Well, many of them were breast cancer patients that were put on a newer chemotherapy agent immunotherapy.
“And they use this same mouse-human line. It’s called VelocImmune, okay. So they took that line and they put this in this chemo-agent. At first, the people looked great. These women were doing wonderfully. ‘I feel good. My tumor shrank.’
“And then what happened within one to three years? Sometimes five but usually one to three years there was an allergic reaction, they called it, and a woman would come back loaded with cancer. All the organs looked like they had melted together. I couldn’t, nor could the radiologist, tell one organ from another. So, it was a fulminant, terrible reaction. This was a failure.
“They’re going to use the same mouse line on people right now. This is horrifying because, although people are only getting one or two of these doses, not many, this can’t be good.”
No, it definitely cannot be good.
As a journalist, it behooves me to always get a second opinion, so I asked some of my sources to verify Dr. Madej’s claims. They checked out with flying colors. In fact, the HEK293T cell line she referred to was also used to develop the Moderna and AstraZeneca vaccines. Stories I read about the cell line on corporate media sites went out of their way to say they definitely did not come from aborted fetal cells even as they admitted that they originated from “donated” fetal cells. It was actually comical seeing the “play on words” Dr. Madej had mentioned in action.
The interview continued to reveal other extremely important information. We even had opportunities to talk about the Bible, a refreshing shift from my normal interviews with other doctors. It was one of my most enjoyable interviews, which is probably why it lasted the full hour.
As I’ve said many times, my preferred regimen is exercise, healthy eating, sunlight, and Dr. Zelenko’s Z-Stack protocol (use promo code “Freedom” for a discount, in case you want to join me in taking the nutraceuticals). While we didn’t discuss the nutraceuticals specifically, Dr. Madej was all onboard with everything else we’re doing to improve our immunity.
It isn’t often I tell people that they NEED to watch a particular interview, but this is clearly one of those rare instances. Dr. Madej’s advice may be life-saving for many.
VIDEO AT LINK..................................
” 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.
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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
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” 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.”
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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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