Posted on 05/03/2021 1:49:29 PM PDT by A.M. Smith
In an exclusive interview with The New American magazine, internationally renowned microbiologist Dr. Sucharit Bhakdi warns that the COVID hysteria is based on lies, adding his voice to the chorus of others like Dr. Tenpenny who say you should avoid the vaccine.
What’s even more alarming is his assertion that the COVID vaccines are set to cause a world-wide cataclysm of unprecedented proportions, including mass death among those who take them.
Starting off, Dr. Bhakdi, the retired chief of the Institute of Medical Microbiology and Hygiene at the University of Mainz, explains that the PCR used to “diagnose” COVID cases has been abused to produce fear in a way that is unscientific.
(Excerpt) Read more at en-volve.com ...
👍🤣💚Lovely Meme—Good job.
Thanks for the ping. Once upon a time there used to be good discussions on FR.
Now it seems like most are trying to be the wise-ackers and who can come up with the best put-downs. Reminds me of an old TV series that featured a group called the sweat-hogs.
And maybe you could answer my question: you think a “vaccine” supposedly put to human trials after only TWO months of the virus even being recorded in the country indicates a well-thought out, well-tested, well-conceived drug?
Or are you one of those people who believe tha vaccine was created long beforehand, in a lab in Wuhan, at the same time as the virus itself?
You accused him of being crazy for thinking a vaccine trial began so early.
He immediately proved you wrong.
Instead of being humbled and apologetic, you follow up with the same question and a wild accusation.
You can do better
Ohhhhh....
My bad!
What are you, his mom? I’m sure he feels safer knowing you’re there to fight his battles for him.
I DID question whether the vaccine had rolled out at all in March, but I ALSO asked him what he would think of a “vaccine” rolled out so early, because I accepted the possibility that maybe something like that HAD rolled out. He didn’t answer that and he’s probably not going to. You up to speed now?
No, it doesn’t seem strange to me. The complete genetic sequence for SARS-CoV-2 was released January 11th. (https://www.cidrap.umn.edu/news-perspective/2020/01/china-releases-genetic-data-new-coronavirus-now-deadly)
SARS-CoV-2 is very similar to SARS-CoV-1 (SARS2003), which had vaccine candidates developed and brought through Phase 1 and Phase 2 clinical trials, but the disease burned out before Phase 3 clinical trials could get funding. However, some work did continue and research into how the body responded to it and how best to combat it generated additional published scientific papers. That included the 2012 paper on the risks of antibody dependent enhancement, which identified specific antigens for the SARS-CoV-1 virus that trigger the suboptimal antibodies.
Multiple studies investigating this all pointed to the S protein as the safest and most effective target for vaccines. Given the similarity between SARS-CoV-1 and SARS-CoV-2, the S protein was the natural starting point for any vaccine work. With the complete genetic sequence for the virus - including the S protein - those taking the mRNA approach merely needed to print out the nucleotide sequence for the S protein and package that in the lipid shell. That reportedly took Moderna 1 weekend to do the actual work. Then there would be pre-clinical trials work to ensure the S protein was produced as expected and filing all the paperwork to begin a Phase 1 clinical trial.
Pfizer actually produced two products in a similar timeframe: BNT162b1 and BNT162b2. They put both through Phase 1 and Phase 2 clinical trials. After that, BNT162b2 was selected for Phase 3 clinical trials because it elicited better responses with fewer side effects. Both were tested on primates in pre-clinical trial challenge trials:
“In the preclinical studies, BNT162b1 and BNT162b2 candidates induced favorable viral antigen specific CD4+ and CD8+T cell responses, high levels of neutralizing antibody in various animal species, and beneficial protective effects in a primate SARS-CoV-2 challenge model.”
The whole point of the third generation vaccines (mRNA platform) is that they’re essentially plug and play. As soon as you identify the antigen you want and have its genetic sequence, you can start producing and testing doses. This doesn’t require any crazy retooling because you’re literally just changing the order and length of the four RNA nucleotides and then packaging that in the same lipid shell. That’s the promise of the new platform is we don’t need to wait months for anything to culture anymore. This is going to enable us to crush Influenza as well. Influenza has always stayed ahead of the vaccines because it takes about 8 months to produce a new vaccine, so whatever was circulating in Asia is what’s used as the basis because there isn’t time to see what actually starts circulating here. With the mRNA vaccines, they’ll be able to target exactly what’s hitting here and get doses in your local Walgreens within a very short period so that instead of 40-60% efficacy, we get north of 90%.
In case you find it useful, I'll put a blob of html below which you can copy and paste into one reply if you like. It includes the movie image and link to the movie. I also made the image clickable - if you click on it the link takes you to the movie page. Let me know if you have any trouble with it or want changes. Again, Thanks!
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