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Kelly Reardon's avatar

Part 2

AFTER the mighty CD8+ Cytotoxic T Lymphocyte cells (AKA Killer T-cells) attack response to modified mRNA transfected cells of tissues & organs inside your body:

After the primary immune system attack response by the cytotoxic T lymphocytes (CTLs), resulting in varying degrees of tissue damage & pathology in different people, a lot happens...

The CTLs will not be able to kill every cell making non-self (spike) protein, so some amount of foreign (spike) protein will get made & released from your cells. That amount will also vary from person to person.

Specialized cells called antigen-presenting cells, especially dendritic cells and macrophages, spring into action. Long story short…you will get serum antibodies made against those foreign proteins which is the stated goal of any shot called a vaccine.

But that can take up to 2 weeks, and during that time, the foreign non-self (spike) proteins are biologically active and will attach to various cellular receptors, resulting in a whole new level of possible tissue destruction.

Now your immune system will activate macrophages & neutrophils that will kill THOSE cells through inflammatory pathways, regardless of whether or not the non-self proteins are toxic themselves.

And if the non-self proteins ARE toxic, like the pathogenic spike proteins, they can cause problems like tissue damage all by themselves without your immune system even being involved at that point.

But your adaptive immune system has done its job & you've made your serum antibodies by now! Yippee!

Too bad those (non-neutralizing, leaky) serum antibodies can only REACT to a (SARS-CoV-2) infection...it is biologically impossible for serum antibodies (in the blood) to PREVENT respiratory infections that enter the body through the mucosa of the mouth/throat, nose, & eyes.

To PREVENT respiratory infections requires a strong innate immune system with mucosal immunity and secretory IgA to stop the respiratory infection at the mucosal and epithelial barriers (stopping the infection OUTSIDE your body and PREVENTING the infection from getting INSIDE your body).

And this is also where the CTLs are supposed to do their cell-destroying activities. When epithelial cells in the mouth/throat, nose, & eyes are infected (like can happen with respiratory diseases) the Killer T-cells will kill those infected cells.

Epithelial cells at the epithelial barrier can be quickly replaced, usually in just a few days in most people. But injections bypass your body's natural protections and send their payload into your body, where that payload can enter your lymph system and bloodstream.

And in the case of the modified mRNA-LNP gene "therapy" injections, this can be disastrous, starting with the immune system attack response against transfected cells of tissues & organs (INSIDE your body) that are now making foreign non-self proteins.

Replacing cells from now damaged tissues and organs inside your body is a complex process that can take weeks or longer, with some areas unable to be repaired at all.

The modification of natural mRNA with synthetic n1-methyl pseudouridine made the modified mRNA longer lasting and resistant to the body’s natural breakdown processes. A Nobel Prize was awarded specifically for this use of longer lasting pseudouridine in the COVID modified mRNA injections.

The synthetic pseudouridine modified mRNA is causing a +1 ribosomal frameshift, as well as a reverse reading, so some people may make spike proteins AND mystery (or junk) non-self proteins.

Studies have found that an antibody subclass switch to IgG4 can occur between mRNA shot #2 & #3, which is sending a stand-down signal to the immune system, essentially telling the immune system to tolerate and ignore the (toxic pathogenic) spike proteins instead of actively fighting to clear the spike from the body.

And people who are getting "booster" after "booster" are repeatedly triggering these immune system activities and causing persistent systemic inflammation, which can cause hyper-immune and autoimmune responses...and then possible immune system exhaustion as your immune system becomes overwhelmed.

Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.

And then there's the plasmid DNA contamination (with the oncogenic SV-40 promotor sequence) that's been discovered. There are a number of ways in which integration into the human genome is possible...

And more...

I am not a doctor…so PLEASE let me know of any corrections that need to be made if I have misstated something…

But tragically, I think the injuries, disabilities, and deaths from these modified mRNA-LNP gene “therapy” injections prove that the COVID shots have been an IMMUNOLOGICAL CATASTROPHE.

Footnote:

Credit to Dr. Sucharit Bhakdi, Dr. Mike Yeadon, & Dr. Kevin Stillwagon for their videos & articles from which I furthered my understanding of human immunology and the essential component of Self vs. Non-self.

Portions of my 2 comments relied on my notes from their work, as well as other doctors' and scientists' work from my over 10,000 hours researching all things "COVID" and the modified mRNA-LNP gene "therapy" injections since 2020. But as I am not a professional researcher, either, I am sorry to say that I neglected to keep proper citations.

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Dr Ah Kahn Syed's avatar

Seems accurate. I would warn against following Mike Yeadon as he rarely publishes referenced material and makes claims that fail verification checks. There is nothing wrong with listening and then going to see if you can verify the claims.

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Markker's avatar

Clearly explained, thanks.

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Kelly Reardon's avatar

You're welcome!

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