Dissolution of Spike Protein by Nattokinase (Peter McCullough)

Far and away the most common question I get from those who took one of the COVID-19 vaccines is: “how do I get this out of my body.” The mRNA and adenoviral DNA products were rolled out with no idea on how or when the body would ever breakdown the genetic code. The synthetic mRNA carried on lipid nanoparticles appears to be resistant to breakdown by human ribonucleases by design so the product would be long-lasting and produce the protein product of interest for a considerable time period. This would be an advantage for a normal human protein being replaced in a rare genetic deficiency state (e.g. alpha galactosidase in Fabry’s disease). However, it is a big problem when the protein is the pathogenic SARS-CoV-2 Spike. The adenoviral DNA (Janssen) should broken down by deoxyribonuclease, however this has not be exhaustively studied.

This leaves dissolution of Spike protein as a therapeutic goal for the vaccine injured. With the respiratory infection, Spike is processed and activated by cellular proteases including transmembrane serine protein 2 (TMPRSS2), cathepsin, and furin. With vaccination, these systems may be avoided by systemic administration and production of Spike protein within cells. As a result, the pathogenesis of vaccine injury syndromes is believed to be driven by accumulation of Spike protein in cells, tissues, and organs.

Nattokinase is an enzyme is produced by fermenting soybeans with bacteria Bacillus subtilis var. natto and has been available as an oral supplement. It degrades fibrinogen, factor VII, cytokines, and factor VIII and has been studied for its cardiovascular benefits. Out of all the available therapies I have used in my practice and among all the proposed detoxification agents, I believe nattokinase and related peptides hold the greatest promise for patients at this time.

I never took any Covid shots. I got a nasty case of Covid every early on, then much later got Omicron. So where does that leave me? How many trillions of spike proteins do you think I have in my body?

Those viruses suckers were all in my tissues with their mRNA instructing my cells to replicate them and their very scary spike proteins.

I'm not an expert in the field by any means, but from what I've read from those who are, and from what I understand of the whole deal, there is a huge difference between immunity based on viral infection and any immunity one might acquire through the mRNA "vaccines" which force your cells to make merely the spike proteins.

As I understand it, when the human immune system begins to produce anti-bodies to a virus, it is keying in, not just on one characteristic of the virus, such as the spike protein signature, but on a number of viral signatures, whereas with the "vaccine" the immune system produces anti-bodies ONLY to the spike protein and nothing else. So, upon any re-infection, the natural immunity has a wider variety of anti-bodies to attack the virus.

If you couple that with the fact that the "vaccine" has inherent risks (all vaccines do, but the evidence suggests strongly that the mRNA vaccines have a much higher injury rate than traditional vaccines, which is to be expected since traditional vaccines are usually run through 7-10 years of trials, while the mRNA "vaccines" had mere months before rolling out) and anyone might arrive at the conclusion that natural immunity is the far better option.

THIS ...

Autopsies Confirm COVID Jab Hazards in Youth

STORY AT-A-GLANCE

When the COVID shots were first introduced, the U.S. Centers for Disease Control and Prevention made several claims about them that have since been proven completely false, including the claim that the mRNA would remain in the injection site, and that both the mRNA and resulting spike protein would rapidly be eliminated from your body
The mRNA goes everywhere and can remain intact for a month of more. Ditto for the spike protein your cells produce

Spike protein has been found in the brains of people with encephalitis (brain inflammation) and in jab-induced shingles lesions. Both mRNA and spike protein have been found in lymph nodes more than 60 days post-jab. Full-length mRNA has also been shown to circulate in people's blood for up to 28 days post-injection, and it's been detected in breastmilk

Research shows the primary difference between those who developed symptoms of myocarditis and those who didn't was that symptomatic patients had markedly elevated levels of full-length spike protein unbound by antibodies in their plasma. Those who remained asymptomatic had no free spike protein in their blood. This would suggest that free-floating spike protein is a problem

Autopsies of two teenage boys found dead in their beds three and four days after their second dose of Pfizer concluded jab-induced heart damage was to blame. The myocarditis described in these instances did not have the typical histopathology of myocarditis. Instead, both cases resemble catecholamine-induced injury, similar to the cytokine storm experienced in severe SARS-CoV-2 infection

https://articles.mercola.com/sites/articles/archive/2023/02/23/autopsies-confirm-covid-jab-hazards-in-youth.aspx

~~~~~

$hot $hills, who are STILL $hilling for these horrid $hots, be darned.

****Note: I pinged JimNoble as perhaps he can answer the question as to whether our immune response is keyed almost exclusively or just mainly to the Spike protein when it comes to enveloped viruses and whether antibodies targeting the Membrane or even possibly Envelope proteins would make a significant difference in immune response. I honestly don’t know, but find it a very, very interesting question and would love to know the answer.****

Thank you for your thoughtful and well-reasoned comment — which made me do some more thinking, too. I am not an expert, either. What you wrote here makes a lot of sense:

>>>”As I understand it, when the human immune system begins to produce anti-bodies to a virus, it is keying in, not just on one characteristic of the virus, such as the spike protein signature, but on a number of viral signatures, whereas with the “vaccine” the immune system produces anti-bodies ONLY to the spike protein and nothing else. So, upon any re-infection, the natural immunity has a wider variety of anti-bodies to attack the virus.”<<<

My understanding, however, is that, when it comes to enveloped viruses, our immune system mainly (almost exclusively?) zeroes in on the spike protein. Is that correct? Well, not being sure whether I remembered correctly, I went and checked (link given later in this post — it’s a very long article I found fascinating, but others may not)):

>>>”Despite a spectrum of differences in their biology and pathogenesis, all enveloped viruses share two commonalities: a lipid bilayer envelope co-opted from host cells upon viral egress and the presence of surface-exposed viral glycoproteins for host cell recognition and entry. These viral glycoproteins or ‘spike’ proteins are exposed to the adaptive immune response and are the main targets of host antibodies, often being the only exposed antigen.” (from page 2 — see also fig. 1 and its accompanying text)<<<

Also:

>>>”The overwhelming majority of antibodies that provide sterilizing protection from infection target the viral spike. Therefore, the structure of the glycoprotein greatly influences how antibodies are selected, matured and specifically interfere with the mechanics of viral entry.”<<<

It appears that one area of vulnerability our antibodies seek to exploit and attack is the area near the base of the “stalk” where the “spike” attaches to the membrane of the virus. So I suppose it might be possible that enveloped viruses’ membrane proteins theoretically *could* have a role — but I really don’t know. When you look at the mechanics of how our antibodies attack and disable the viruses’ machinery, it does not seem likely to be significant to me, but again, I am not a doctor or microbiologist.

Link to article:

Antibody responses to viral infections: a structural perspective across three different enveloped viruses

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6818971/#!po=5.22388

Classic view link (easier to search):

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6818971/?report=classic

I can see why they chose the spike protein, given the above. Of course no one wanted to mess with a vaccine using the whole virus considering the disastrous results of the SARS1 vaccine animal tests:

https://pubmed.ncbi.nlm.nih.gov/22536382/

Link to list of proteins expressed by the Covid virus:

>>>>”In addition to these genes, SARS-CoV-2 contains genes that encode four structural proteins which are involved in infectious virus assembly: (S)pike, (E)nvelope), (M)embrane, and (N)ucleocapsid) proteins. The N protein holds the RNA genome, and the S, E, and M proteins together create the viral envelope. The spike protein is responsible for allowing the virus to attach to and fuse with the membrane of a host cell. Interspersed between these genes in the coronavirus genome are several other genes called “group-specific or accessory genes” and their gene products are called “accessory proteins” that are dispensable for virus growth in vitro, but may play an important role in modulating the host response to virus infection and thereby, contribute to pathogenesis.”<<<<

https://www.ncbi.nlm.nih.gov/Structure/SARS-CoV-2.html

Um, no, that is not how the Covid vaccines work. They certainly *do not* protect you from all Coronaviruses. They weren’t even very effective against Covid variants, especially the Omicron variants.

The reason we can catch “the common cold” caused by Corona viruses over and over again is the little devils love to mutate and therefore our natural immunity to an earlier iteration is not very effective against a newer variant.

There were no Spike proteins in the vaccines. There were snippets of mRNA encased in a lipid envelope (to keep the fragile mRNA from degrading before it could do its thing) that encoded “instructions” for our cells to produce the Covid virus’ Spike protein minus its harmful bit.

The condition called ADE occurred after animals vaccinated with experimental vaccines for SARS1 (Covid’s older, much nastier cousin) were challenged with the live virus after vaccination. Those vaccines either contained whole virus or whole Spike protein. See link in my post #78:

https://freerepublic.com/focus/chat/4133137/posts?page=78#78

Disclaimer: Opinions posted on Free Republic are those of the individual posters and do not necessarily represent the opinion of Free Republic or its management. All materials posted herein are protected by copyright law and the exemption for fair use of copyrighted works.