Shot-to-Death Immune systems By Brian Simpson

Here is what I could find about a paper written by scientists from the famous Wuhan Institute of Virology, where it all started, many propose, reporting that patients who experienced severe SARS-CoV-2 symptoms also had “lymphopenia.” Lymphopenia is the depletion of the major immune T lymphocyte cells, caused by apoptosis, or the cellular suicide, of T cells after infection. These observed immune suppressing results are consistent with observations by other Covid researchers and practicing doctors, such as Dr Zev Zelenko, who has said: “And so that’s why there’s a huge spike in cancers. A huge spike in autoimmune diseases, opportunistic infections. Not to mention blood clots, heart attacks, strokes, myocarditis, miscarriages, ovarian testicular dysfunction, most likely infertility and antibody-dependent enhancement.” Dr Zelenko is referring to the effects of the Covid vaccines, but it is academic, since the majority of Covid infections now are occurring in the multiple vaxxed.

The real Covid crisis is just unfolding.

https://www.naturalnews.com/2022-03-23-people-shot-immune-systems-to-death-vaccines.html

“A paper written by scientists from the Wuhan Institute of Virology claimed that many patients who experienced severe SARS-CoV-2 symptoms also had “lymphopenia,” which is the depletion of all the important immune T lymphocyte cells. This depletion was caused by apoptosis, or the cellular suicide, of T cells after infection.

The attraction to T cells and the ability to infect them were unrelated to the usual way that the COVID virus infects other cells, such as lung cells, because T cells do not have the needed receptors.

However, SARS-CoV-2 destroys the immune T cells similar to the way the human immunodeficiency virus does.

The lymphocytes are the cells responsible for killing infected or cancerous cells. They are a type of white blood cells that protect the body against cancerous cells and those that have become infected by pathogens, such as bacteria and viruses.

These T cell lymphocytes develop from the stem cells in the bone marrow, and they migrate to the thymus via blood. The thymus is part of the lymphatic system that functions mainly to promote the development of mature T cells, which are necessary for cell-mediated immunity. This is a type of response that involves the activation of the immune cells to fight infection. T cells function to actively destroy infected cells and signal others to participate in the immune response.

Research shows dramatic declines in T cells

The paper further showed that there are dramatic declines in T cells as well as CD4 and CD8 cells.

In explaining how they performed genetic tests to make sure that the T cells actually get infected, the researcher said they analyzed the presence of SARS-CoV-2 viral antigens in PBCs using flow cytometry. The results suggested that T lymphocytes were infected, and in a certain patient, T cells also showed high infection rates. The team also confirmed the presence of viral antigen in T lymphocytes from patient blood.

In preparing postmortem lung sections from patients with fatal injections, they were able to analyze T lymphocytes infiltration and virus infection and found that T lymphocytes infiltration in the lung section was also positive for SARS-CoV-2 NP staining, indicating that the virus has infected the lung.

Taken together, it showed the presence of SARS-CoV-2 viral antigen in T lymphocytes either in the blood or in the lungs section of COVID-19 patients.

According to the researchers, HIV also uses the same receptor as SARS-CoV-2 to enter lymphocytes and the same gp120 protein to facilitate its entry into the cells, making their effect on lymphocytes similar in many ways.

AIDS, cancer from vaccines

There had also been reports of the COVID vaccines causing cancer and vaccine-induced AIDS at an alarming rate. Three whistleblowers managed to acquire data from the Department of Justice about the COVID-19 vaccines and their adverse effects.

One of these whistleblowers is physician Ryan Cole, who also spoke at Wisconsin Senator Ron Johnson’s COVID panel earlier this year. Cole said he noticed certain viruses increasing, while only a limited number of T cells keep cancers in check. In the 40,000 biopsies that he did in the past year, Cole said he’s seen many types of cancers in vaccinated individuals.

Dr. Zev Zelenko, who speaks of the negative effects of the COVID vaccines, said that a jab could damage the tumor suppressor genes, and people are essentially killing their immune systems.

“And so that’s why there’s a huge spike in cancers. A huge spike in autoimmune diseases, opportunistic infections. Not to mention blood clots, heart attacks, strokes, myocarditis, miscarriages, ovarian testicular dysfunction, most likely infertility and antibody-dependent enhancement,” he said.”

https://www.naturalnews.com/2022-03-23-spike-protein-covid-vaccines-most-bioactive-damaging.html

https://igorchudov.substack.com/p/sars-cov-2-kills-t-cells-just-like?s=r

 

“Is Sars-Cov-2 airborne HIV? Two days ago, an interesting article came out:

This article was not written by a bunch of random scientists, but instead was written by people from the Wuhan Institute of Virology, including the infamous batwoman Shi Zheng-Li. Just keep this in mind. It was originally submitted in Sep 2021 and revised in January 2022, so it does not involve Omicron.

The article is saying the following:

  • Many patients who had severe Sars-Cov-2 had “lymphopenia”, that is, depletion of the all important immune T lymphocyte cells
  • This depletion was caused by cellular suicide (apoptosis) of T cells after infection
  • In experimental setups involving infecting laboratory cell lines of human T cells, Sars-Cov-2 virus was able to penetrate and infect T cells
  • This tropism (attraction to) T cells and ability to infect them was UNRELATED to the usual way Sars-Cov-2 infects other cells, such as lung cells, that express ACE2 and TMPRSS2 receptors, because T cells do not have those receptors.
  • Infection of T cells occurs via “LFA-1, the protein [that] exclusively expresses in multiple leukocytes”
  • It turns out that HIV’s gp120 protein is the one that “Activates LFA-1 on CD4 T-Lymphocytes and Increases Cell Susceptibility to LFA-1-Targeting Leukotoxin
  • I would like to remind you that HIV’s gp120 protein also was mysteriously transplanted into Sars-Cov-2
  • Additionally, gp120 protein is located in the spike protein of Sars-Cov-2, and spike protein is used in all “Covid vaccines”.

So, now we have a full new mystery: Sars-Cov-2 destroys immune T cells just like HIV does, Sars-Cov-2 has a transplanted gp120 HIV insert, and it is that specific gp120 insert that allows HIV to enter lymphocytes via the same LFA-1 receptor

Let’s look at this more closely:

Lymphopenia

T Lymphocytes are cells that are responsible for killing infected or cancerous cells.

T cells are a type of white blood cell known as a lymphocyte. Lymphocytes protect the body against cancerous cells and cells that have become infected by pathogens, such as bacteria and viruses. T cell lymphocytes develop from stem cells in bone marrow. These immature T cells migrate to the thymus via the blood. The thymus is a lymphatic system gland that functions mainly to promote the development of mature T cells. In fact, the "T " in T cell lymphocyte stands for thymus derived.

T cell lymphocytes are necessary for cell mediated immunity, which is an immune response that involves the activation of immune cells to fight infection. T cells function to actively destroy infected cells, as well as to signal other immune cells to participate in the immune response.

HIV and Sars-Cov-2 Use gp120 to Enter T cells

The primary mechanism of AIDS is depletion of CD4 cells. For Sars-Cov-2, we see depletion of CD4 and CD8 cells as well. Science has long answered how HIV infects T cells (1991):

The news here is that Sars-Cov-2 also infects T cells, and Sars-Cov-2 also has the gp120 insert:

LFA-1 Receptor

Remember that for the last two years we have heard how Sars-Cov-2 infects cells expressing ACE-2 receptor ad TMPRSS2 protein. Guess what, our T-cells have neither of those!

So, how do they get infected? The WIV article that I am discussing, conveniently, found the mechanism: it is a so called LFA-1 receptor.

Amazingly enough, if you still believe in coincidences, HIV also uses the same LFA-1 receptor to enter lymphocytes, and uses the same gp120 protein to facilitate the entry.

Summary

From the articles cited, we can see that

  • Covid-19 causes lymphocytopenia (depletion of lymphocytes) in real life patients
  • HIV causes depletion of lymphocytes also
  • Both Sars-Cov-2 and HIV use the same receptor LFA-1 to enter T cells
  • HIV uses gp120 protein to bind to LFA-1 receptor
  • Sars-Cov-2 also has gp120 insert as well, mysteriously

And, therefore, the effect of Sars-Cov-2 and HIV on lymphocytes is in many ways similar.

The bats, sitting in Chinese caves a thousand miles from WIV, were clearly very smart when they decided to add gp120 to their natural coronaviruses!”

 

https://www.naturalnews.com/2022-03-15-fauci-patent-gp120-covid-hiv-destroys-t-cells.html

 

 

 

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Sunday, 13 October 2024

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