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To: grey_whiskers

It shameful you have to call me a moron. My comment did not say anything about “the mechanism of blood vessel damage in coof-patients.”

You wrote, “The Pfizer/BioNTech and Moderna Covid-19 vaccines are genes therepy.” For a discussion on the nature of them, go to this “Forbes” article:

https://www.forbes.com/sites/brucelee/2021/03/17/covid-19-mrna-vaccines-are-not-gene-therapy-as-some-are-claiming/?sh=4fdd1d203d20

You misinterpreted what I said the dendrite cells do to the Spike Protein which is in the RMA form. Once the lipid nanoparticle delivers the RNA version of the Spike Protein to the cell’s ribosomes the translation process transforms it into the RNA version. That RNA is broken up in segments which are presented on the cell’s surface where they bind to the MHC-1 and MHC-2 complex molecules. It is at these sites where they trigger events leading to the creation of antibodies programmed to hunt down Spike Proteins. With that function done, the host cell is destroyed will no longer create Spike Proteins. So, if there are any loose Spike Proteins in the ovaries, spleen, bone marrow, liver, adrenal glands and the brain, they are destroyed by the antibodies. And no way do they invade the cell through the ACE-II receptor. Where do you get that idea?

Here is a good explanation of how it all happens. The fellow presenting it is quite enjoyable in his presentation:

https://www.youtube.com/watch?v=35Idb_lCU4o


182 posted on 07/04/2021 10:26:54 PM PDT by jonrick46 ( Leftnicks chase illusions of motherships at the end of the pier.)
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To: jonrick46
It shameful you have to call me a moron.

What is shameful is your post. You do realize you left out the word "is" in your deft masterstroke of a retort, don't you? My comment did not say anything about “the mechanism of blood vessel damage in coof-patients.”

Yes, it did. Cut-and-paste:

*The spike protein from SARS-CoV-2 alone is the main cause of blood vessel damage in COVID-19 patients.

(I think that was your post #109 this thread.)

Either you're a pathological liar.

Or you're a troll.

Or you have no idea what in the hell you post and change what you say from reply to reply.

I don't care what Forbes said; I the mRNA jab is considered an experimental gene therapy by the FDA; Moderna admitted as much in their SEC filing about a year ago. On or about page 70, IIRC.

You misinterpreted what I said the dendrite cells do to the Spike Protein which is in the RMA form.

DAFUQ? You must be inhaling too many fireworks fumes.

I just googled "MRA form spike protein" and got NOTHING about it.

Your next sentence isn't any better.

VERBATIM cut and paste, again:

Once the lipid nanoparticle delivers the RNA version of the Spike Protein to the cell’s ribosomes the translation process transforms it into the RNA version.

So the RNA version of the spike protein is delivered to the ribosomes and the translation process transforms it into the RNA version. Umm, yeah.

Then supposedly, the RNA itself is broken into segments which are presented on the cell's surface where they bind to the MHC-1 and MHC-2 complex molecules.

So the spike protein disappears, and fragments of the DNA go to the cell's surface, sure, whatever you say.

(At least MHC-1 and MCH-2 are real.)

It is at these sites where they trigger events leading to the creation of antibodies programmed to hunt down Spike Proteins. With that function done, the host cell is destroyed will no longer create Spike Proteins.

Umm, Einstain. The cell which was producing the spike proteins, stops making the spike proteins, when the mRNA itself is degraded.

So, if there are any loose Spike Proteins in the ovaries, spleen, bone marrow, liver, adrenal glands and the brain, they are destroyed by the antibodies. And no way do they invade the cell through the ACE-II receptor. Where do you get that idea?

We don't know for sure all of them are destroyed by the antibodies. And they do *bind* to the ACE-II receptor, though the mRNA itself has supposedly made changes to the spike protein to be produced after the jab, so that it will no longer merge with the cell membrane (which is how the actual virus effectuates entry into the cell). The issue then becomes one of various inflammatory signaling enzymes being released because of the interaction with the spike protein, any damage caused by the body chewing up cells with the spike protein on their membrane, and the spike protein inducing abnormal clotting all by itself.

This isn't even like shooting fish in a barrel anymore. You're just making random things up "Because SCIENCE!"™

183 posted on 07/04/2021 11:19:48 PM PDT by grey_whiskers (The opinions are solely those of the author and are subject to change with out notice.)
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