Originally posted by /u/veganmark:

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This article by Steve Kirsch posted here yesterday makes some interesting points, one of which I would like to discuss:

https://stevekirsch.substack.com/p/robert-malones-doctor-had-her-license

Here is one of the (true) statements which Dr. Nass made that motivated the medical authorities in Maine to deprive her of her medical license:

“If you’re going to get myocarditis over 80% get it after the second dose, not after the first dose” and “people who got it after the first dose, many of them had already been infected with COVID”

This observation is completely consistent with an autoimmune origin for the myocarditis that these vaccines are evoking. After the first shot, some cells in the heart incorporate the vaccine mRNA and start making spike protein. But it takes days, possibly weeks following vaccination for killer T lymphocytes capable of recognizing protein fragments derived from the spike protein to develop. And by the time they do, the modified mRNA taken up by the heart has been largely degraded, and spike protein production has fallen off. So no major autoimmune issue at this point.

But when you get the NEXT vaccination - or a booster - the killer T cells that recognize spike protein as foreign are all revved up and ready to go; this means that almost instantly they can attack and kill cells in the heart (or other tissues) that they view as foreign.

If a person has already had COVID, chances are good that they already have killer T cells that can recognize spike protein peptides - which is why these people tend to experience myocarditis after the first shot. It all adds up. And it also why vaccinating people who have already experienced COVID infections is batshit crazy.

Let me explain this a little better. One of the key weapons in our immune arsenal are cytotoxic (or killer) T lymphocytes. Their function is to hunt down and kill cells that are making one or more proteins that are foreign to the body. Virally infected cells do this, and killer T cells, by eliminating these cells, can suppress further spread of the virus. And many cancer cells make mutated proteins that killer T cells can recognize as foreign; by killing such cells, killer T cells protect us from cancer spread.

When mRNA vaccines were developed, it was not the intent of the developers that the injected nanoparticles would reach the bloodstream and circulate through the body. Typical protein vaccines are metabolized in the injected muscle and draining lymph nodes, and it was assumed that these mRNA vaccines would do the same. But preclinical Japanese research that became public about a year ago demonstrated that, shockingly, the injected nanoparticles were entering the bloodstream, and could deposit their mRNA in cells throughout the body.

When I first read this, my reaction was: WTF?!! Because this evidently implies that cells throughout the body would become targets for killer T lymphocyte attack. I mean, this strategy seems insane ON ITS FACE. But, since no one was raising the issue at the time, and these vaccines were alleged to be proven "safe and effective", I let myself think that, perhaps these vaccines do a poor job of evoking killer T lymphocytes, or something else is going on that makes these vaccines less dangerous than I suspected.

The recent demonstration by pathologist Dr. Arne Burkhardt, who did autopsies of people who had died soon after vaccination, and found that killer T lymphocytes were INDEED attacking vascular cells at the time of their deaths, made me realize that my initial reaction was right on target. And the fact that vascular endothelial cells are probably taking up most of the circulating vaccine nanoparticles, and then become susceptible to immune attack, can readily explain the high risk for thrombotic complications in people getting vaccinated with these agents.

The fact that some people have severe, something lethal reactions to these vaccines, whereas most others skate by without evident harm might be explained by variables such as: to what extent do the injected nanoparticles enter the circulation; where are they chiefly taken up; how long is the injected mRNA viable; to what extent does vaccination induce killer T cells that recognize spike protein peptide fragments; and the pre-existing health status of the individual - an autommune attack on the endothelium overlying soft arterial plaque could readily trigger a heart attack or stroke, but this mechanism wouldn't be relevant to healthy people who have no such plaques.

Let me make it clear that what I am talking about here is the most ELEMENTAL immunology. The fact that killer T cells function to attack and kill cells expressing foreign proteins is something you would learn in the FIRST WEEK of a basic immunology course. There is literally ZERO excuse that this issue hasn't been addressed by the "medical authorities" forcing these vaccines on us. What we are dealing with here is medical malpractice of the most cataclysmic magnitude.