https://www.zerohedge.com/covid-19/california-counties-see-covid-cases-rising-most-heavily-vaccinated-counties?commentId=807116db-55ee-4ab0-ac2d-204d576e59a3
Collection of links posted on ZH at the comment link above.
spike protein shedding machines!
Spike protein is a bioweapon…
Spike protein in the vaccine is cytotoxic
The Cytotoxic Effects of Spike Proteins and Hydroxychloroquine
And in case you wanted to “fact check”
https://www.reuters.com/article/factcheck-vaccine-cytotoxic-idUSL2N2O01XP
…but if you “fact check” the fact checkers…you end up here –
…and if you review those data sources…you’ll see a number of conflicts of interest (like entities that own some of the patents)…but among those sources…
https://blogs.sciencemag.org/pipeline/archives/2021/05/04/spike-protein-behavior
…and if you follow the source for that…
SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2
” In the current study, we show that S protein alone can damage vascular endothelial cells (ECs) by downregulating ACE2 and consequently inhibiting mitochondrial function.”
https://www.ahajournals.org/doi/full/10.1161/CIRCRESAHA.121.318902
…and of course minimized by the author who ironically..
“Lowe was the one of the first people to blog from inside the pharmaceutical industry, with the approval of his supervisor and the company legal department”
https://en.wikipedia.org/wiki/Derek_Lowe_(chemist)
Cytotoxicity is cell death.
Pfizer distribution study
Dr. Byram Bridle, an Associate Professor on Viral Immunology at the University of Guelph suggests there may be terrifying reasons side effects such as heart inflammation, VITT, and other serious issues may occur in those who have been vaccinated.
https://omny.fm/shows/on-point-with-alex-pierson/new-peer-reviewed-study-on-covid-19-vaccines-sugge
I am a pediatric specialist caring for children with the multisystem inflammatory syndrome (MIS-C). I am concerned about the possibility that the new vaccines aimed at creating immunity against the SARS-CoV-2 spike protein (including the mRNA vaccines of Moderna and Pfizer) have the potential to cause microvascular injury to the brain, heart, liver, and kidneys in a way that does not currently appear to be assessed in safety trials of these potential drugs.
Is it possible the spike protein itself causes the tissue damage associated with Covid-19? Nuovo et al (in press) have shown that in 13/13 brains from patients with fatal COVID-19, pseudovirions (spike, envelope, and membrane proteins) without viral RNA are present in the endothelia of cerebral microvessels. Furthermore, tail vein injection of the full length S1 spike subunit in mice led to neurologic signs (increased thirst, stressed behavior) not evident in those injected with the S2 subunit. The S1 subunit localizes to the endothelia of microvessels in the mouse brain, and is a potent neurotoxin. So the spike S1 subunit of SARS-CoV-2 alone is capable of being endocytosed by ACE2 positive endothelia in both human and mouse brain, with a concomitant pauci-cellular microencephalitis that may be the basis for the neurologic complications of COVID-19. The Pfizer/BioNTech vaccine (BNT162b2) is composed of an mRNA that produces a membrane-anchored full-length spike protein. The mouse studies suggest that an untruncated form of the S1 protein like this may cause a microvasculopathy in tissues that express much ACE2 receptor.
While there are pieces to this puzzle that have yet to be worked out, it appears that the viral spike protein that is the target of the major SARS-CoV-2 vaccines is also one of the key agents causing the damage to distant organs that may include the brain, heart, lung, and kidney. Before any of these vaccines are approved for widespread use in humans, it is important to assess in vaccinated subjects the effects of vaccination on the heart (perhaps using cardiac MRI, as Puntmann et al. did). Vaccinated patients could also be tested for distant tissue damage in deltoid area skin biopsies, as employed by Magro et al. As important as it is to quickly arrest the spread of the virus by immunizing the population, it would be vastly worse if hundreds of millions of people were to suffer long-lasting or even permanent damage to their brain or heart microvasculature as a result of failing to appreciate in the short-term an unintended effect of full-length spike protein-based vaccines on these other organs.
https://www.regulations.gov/document/FDA-2020-N-1898-0246
Almost half the people hospitalized because of covid-19 have blood or protein in their urine, indicating early damage to their kidneys, said Alan Kliger, a nephrologist at the Yale School of Medicine who co-chairs a task force assisting dialysis patients who have covid-19.
….my neighbor died on the 18th of kidney failure about 3 months after getting the 2nd shot…never got sick with Covid…but he did get the vaccine.
Here we provide evidence that circulating SARS-CoV-2 proteins are present in the plasma of participants vaccinated with the mRNA-1273 vaccine. We report antigen and serological data of the mRNA-1273 vaccine in 13 healthcare workers at the Brigham and Women’s Hospital.
https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciab465/6279075
The S1 protein of SARS-CoV-2 crosses the blood–brain barrier in mice
https://www.nature.com/articles/s41593-020-00771-8
The SARS-CoV-2 spike protein alters barrier function in 2D static and 3D microfluidic in-vitro models of the human blood–brain barrier
https://www.sciencedirect.com/science/article/pii/S096999612030406X
The S1 subunit causes degeneration of endothelial cells and motor neurons in cell culture. The S1 subunit alone when injected into mice causes a systemic endothelialopathy. Damage to ACE2+ endothelial cells is the key feature of human COVID-19 and the mouse model of the disease.
https://www.sciencedirect.com/science/article/abs/pii/S1092913420302288?via%3Dihub
Blood-brain barrier function is negatively affected by SARS-CoV-2 spike protein subunits.
https://www.sciencedirect.com/science/article/pii/S096999612030406X#bb0250