Detective work ensued.
Some scientists have said that the spike was chosen because it is the protein that binds to host cells, and thus it is the only part of the virus that can elicit "neutralising antibodies" that help prevent infection.
If you didn’t know, neutralising antibodies not only bind to a virus, they bind in a manner that blocks infection. Only a small subset of the many antibodies that bind a virus are capable of neutralisation.
And yes, the spike protein is capable of eliciting neutralising antibodies, and though I have researched this thoroughly, I could not find evidence of other parts of the virus having the ability to do the same thing. Remember that this doesn’t rule out the possibility that they can’t however. It just hasn’t been tested.
So spike was chosen to elicit neutralisation, okay, or as one paper puts it, “S glycoprotein is responsible for the entry of the virus into host cells, where it begins to spread, but it can also be recognized by the immune system triggering a protective response, the main objective of vaccines. Several types of new vaccines currently in use are selected based on their ability to generate neutralizing antibodies upon immunization.”.
This would be all well and good but as we know now, mRNA-vaccine-induced neutralising antibodies are highly variable among individuals. In other words… useless. This should have been tested thoroughly before mass introduction don’t you think?
Spike is also rapidly mutating and evades vaccine-induced antibodies with high efficiency. So again, useless.
And what makes this all so potentially sinister is that the spike protein is extremely toxic, regardless of what certain ‘fact checkers’ have said in the past.
The spike protein is definitely toxic. We know it can cross the blood-brain barrier in mice and cause nerve damage. We know it can cause cardiac damage. We know it can cause lung inflammation. We know it can cause endothelial cell damage. We know it can significantly inhibit DNA damage repair.
You get the point. (Click on those hyperlinks if you don’t believe me)
Also remember that the COVID lab-leak hypothesis, the hypothesis regarding whether or not SARS-CoV-2 coronavirus emerged from a laboratory and was subsequently leaked, has not been disproven as of yet.
I bring this up because it has been found that the SARS-CoV-2 spike protein (both the natural and mRNA kind) has GP120 (Panglolin HIV) and Staphylococcus Enterotoxin B (SEB) gene inserts.
That’s the human immunodeficiency virus HIV. One study, now withdrawn, noting the GP120 inserts states, “Taken together, our findings suggest unconventional evolution of 2019-nCoV that warrants further investigation.”. I ditto that.
And the symptoms of SEB intoxication is noted in one review titled ‘Staphylococcal Enterotoxin B as a Biological Weapon: Recognition, Management, and Surveillance of Staphylococcal Enterotoxin’, like the following,
“sudden onset of fever (40-41C), chills, headache, myalgia, non-productive cough. Some patients may develop shortness of breath and chest pain. Fever may last for 2-5 days and cough may continue for up to one month. Patients also present with nausea, vomiting, and diarrhea when the toxin is swallowed.”.
Now, what does that sound like?
So I ask again, why spike protein?
Why not use other proteins, a weaker spike, or a...
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2 comments:
An excellent post. Thank you for this resorce.
Why? Assuming that is a viable choice? What about reducing the carbon footprint you are wearing do you not understand?
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