Another Study Finds mRNA Vaccines Impair the Immune System

Study in Clinical And Experimental Medicine Journal

Four years after the biggest human experiment began, scientists are confirming what they already knew. mRNA vaccines have never been approved before because they always fail on this key point that scientists are re-confirming over and over again.

This latest study was published in Clinical and Experimental Medicine and was called mRNA vaccine boosters and impaired immune system response in immune compromised individuals: a narrative review.

Scientists reviewed multiple studies assessing if frequently repeated COVID-19 mRNA booster shots could impair immune systems, especially in people with compromised immunity. The very people that need protection.

They begin by saying:

Over the last 18 months, there has been growing evidence of a correlation between the increased prevalence of COVID-19 infection and other pathologies, and the repetition of mRNA COVID-19 vaccine boosters. Recent works are now evidencing causation to add to correlation, as multiple doses of the mRNA COVID-19 vaccines may result in much higher levels of IgG 4 antibodies, or also impaired activation of CD4 + and CD8 + T cells.

They note that “undesirable outcomes observed after vaccination may be associated with the proinflammatory properties of the lipid nanoparticles or the delivered mRNA in the vaccine formulation”.

According to one of the papers reviewed, already in 2021, “the immune function was better among unvaccinated individuals than vaccinated individuals 8 months after the administration of the two doses of the mRNA COVID-19 vaccine”. Even the EU Medicine Agency warned about the impact of repeated boosters on the immune system.

“Reduced cellular immunity may be the unexpected consequence of having replaced uracil in the genetic code with N1-methyl pseudo uridine”. This means that changes to the genetic code may have ended up activating a specific type of immune cell in the body called regulatory T cells. These T cells in turn suppress broader immune defences, potentially reducing immune protection against the virus.

The report highlights what we all know, that the vaccine was never supposed to stay in the arm but was actually targeted towards lymph nodes and the spleen. “This is central to explaining the many side effect which include the unintended consequences on the immune system. The lipid nanoparticles encapsulating the mRNA of the COVID-19 vaccines build up in the liver, spleen, adrenal glands and ovaries. The lipid nanoparticle component is highly inflammatory.”

Cells that are primed to produce the spike protein are damaged. Spike proteins in the bloodstream damage endothelial cells. SARS-CoV-2 spike protein antibodies may have unintended consequences on other spike proteins. The residual immune memory of the original SARS-CoV-2 virus may prevent efficacy against variants. Signs of reduced immune system response have been many.

It also discussed a paper that provides evidence suggesting that the vaccine can significantly disrupt type I interferon signalling, leading to various adverse effects on human health. For example, they can tamper with control systems balancing protein production and monitoring for cancerous cells.

Such disruptions from widely-travelling exosomes may help explain various side effects reported after COVID vaccination. These span from neurodegenerative brain conditions to heart inflammation, blood clotting disorders, facial paralysis, liver disease, DNA instability, impaired viral immunity, and cancer progression.

In other words, an unintended effect of the mRNA vaccines appears to be production of spike protein-containing exosomes interfering with cell regulation body-wide. They say that this hypothesis is supported by evidence from the VAERS database.

The researchers also explain something I have written a lot about - that getting multiple mRNA COVID-19 vaccine booster shots can lead to high levels of a specific antibody called IgG4 building up in the body. IgG4 antibodies also have an unusual "swap" ability allowing them to exchange binding regions with other IgG4s. This swap makes them less effective at reliably binding target virus particles to block infection.

While some IgG4 is normal, too much IgG4 puts people at higher risk from COVID-19 complications. Very high IgG4 levels were linked before to more severe infection outcomes. The authors conclude repeated mRNA vaccination boosters may overtrigger IgG4 antibody production. This can essentially "distract" and misdirect the immune response instead of strengthening it. In some people already prone to inflammation, autoimmunity, or cancer, excess IgG4 from repeat boosters could promote development of those disease conditions.

Finally, the paper looked at T cells. Repeated COVID mRNA vaccine boosters can impair critical immune cells called CD4+ T cells and CD8+ T cells. An animal study found giving excessive extra booster doses decreased antibodies against variants. It also exhausted T cell activation that normally fights infection.

Impaired CD4 + T cell activation, as seen in conditions like HIV/AIDS, can result in a higher risk of opportunistic infections. For example, mycosis fungoides, which is a type of cutaneous T-cell non-Hodgkin's lymphoma, is characterized by the abnormal accumulation of CD4 + T cells in the skin.

CD4+ cells orchestrate immune responses while CD8+ cells directly eliminate infected cells. With impaired CD4+ and CD8+ cell action, the body becomes vulnerable to viruses, uncontrolled inflammation, and cancer growth. This study confirmed recurrent boosters override previous vaccine immunity to actually promote tolerance. So excessive boosters may backfire, enabling illnesses instead of preventing them.

One of the final sentences in the paper is something you would have been banned for saying in 2021 - “Natural immunity is far superior to that achieved by vaccination, as well-known since 2021”.