The spike protein of the virus, that is also being utilized in the vaccines, is damaging to our cells through 3 mechanisms. The first is that when the spike protein binds to the ACE2 receptor it causes the ACE2 to send signals to the mitochondria within the cell which destroys the mitochondria, eventually killing the cell. The second is that when the spike protein binds to our ACE2 receptors it causes the ACE2 to send signals to other cells which increases the amount of pro-inflammatory agents in the blood. This inflammation damages the tissues.
The third way is that when the spike protein binds to the ACE2 of the platelets in our blood, it causes them to clot. Now, the vaccine manufacturers did take steps to make the spike protein more safe. The spike protein has two parts an S1 subunit and an S2 subunit. The S1 is the part that connects to the ACE2, and the S2 is the part that opens up like a knife stabbing the membrane and facilitates fusion between the membrane of the cell and the envelope of the virus.
With the vaccines, they modified the S2 subnit so that it could not open up and jab into the cell membranes if it connects with any ACE2 receptors. They thought this would make the spike protein safe, but this assumption is false and if they had taken the time to do more research before rushing to production they would have found that out. It may seem like the jabby bit is what damages the cells, but actually the major damage is caused by the S1 connecting to the ACE2 receptor. Just the S1, by itself without the S2, causes the ACE2 receptor to start the cell signaling processes that cause the mitochondrial damage, the pro-inflammatory response, and the blood clots.
“The COVID-19 vaccines did not save lives and appear to be lethal toxic agents – the vaccines did not reduce serious illness (as claimed by manufacturers) enough to reduce any risk of death. In the 17 countries of the present study, there is no evidence”
September 2023 COVID-19 vaccine-associated mortality in the Southern Hemisphere Denis G. Rancourt,1, * PhD ; Marine Baudin,2 PhD ; Joseph Hickey,1 PhD ; Jérémie Mercier,2 PhD 1 Correlation Research in the Public Interest (correlation-canada.org) 2 Santé Liberté OÜ (jeremie-mercier.com)
Studies on the spike protein:
- How the virus uses the spike protein to enter human cells: https://www.nature.com/articles/d41586-021-02039-y
- Article on how the Covid19 spike protein crosses the blood-brain barrier: https://www.sciencedirect.com/science/article/pii/S096999612030406X?via%3Dihub
- Japanese article on how the Pfizer vax is associated with brain hemorrhaging (lending credence to the hypothesis that the spike proteins are crossing the blood brain barrier in some people): https://joppp.biomedcentral.com/articles/10.1186/s40545-021-00326-7
- Article on how AstraZeneca is associated with blood clots in the brain (lending more credence to the hypothesis that the spike proteins are crossing the blood brain barrier in some people): https://www.nejm.org/doi/full/10.1056/NEJMoa2104840
- Article on how the Covid19 spike protein binds to the ACE2 receptor of our platelets to cause bloodclots: https://jhoonline.biomedcentral.com/articles/10.1186/s13045-020-00954-7
- Article explaining that blood clots from the spike protein interacting with our platelets are associated with both COVID-19 infection and vaccination: https://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.1003648
- Article explains that just the S1 subunit of the spike protein can cause platelets to clot: https://www.medrxiv.org/content/10.1101/2021.03.05.21252960v1
- Article with evidence that spike proteins do end up circulating in the blood, when they’re not supposed to, they’re supposed to be anchored on the cell membranes: https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciab465/6279075
- More evidence that spike proteins do not stay on the cell membranes but end up circulating in the blood. This study aims to explain the blood clots caused by the J&J and AstraZeneca adenovector vaccines, they claim that the DNA isn’t properly spliced and the spike proteins end up in the blood causing thrombosis when the spikes attach to the ACE2 receptors of the endothelial cells: https://www.researchsquare.com/article/rs-558954/v1
- Article on how the spike protein can cause neurodegeneration: https://www.sciencedirect.com/science/article/pii/S0006291X2100499X?via%3Dihub Journal article with evidence that the spike protein by itself can
- damage cells by binding to ACE2, causing the cells mitochondria to lose their shape and break apart: https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.121.318902
- Article on how the spike protein in vaccines can cause cell damage via cell signaling: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827936/
- Article that when the spike protein binds to the ACE2 receptor it causes the release of soluble IL-6R which acts as a extracellular signal which causes inflammation (see the first paper for evidence that the spike causes the release of IL-6R and see the second paper for an explanation of how soluble IL-6R causes pro-inflamatory extracellular signaling: https://pubmed.ncbi.nlm.nih.gov/33284859/
- And https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491447/
- Another article that Spike protein from covid or the vaccine causes inflammation through cell signaling, this time there is evidence that the spike protein causes senescence (premature aging) signals in the cell which attracts leukocytes that cause inflammation of the cell: https://journals.asm.org/doi/10.1128/JVI.00794-21
- Spike protein by itself causes cell damage by eliciting a pro-inflammatory response: https://www.nature.com/articles/s41375-021-01332-z