1/ This research proves that the mRNA vaccines induce circulating Spike protein (not localized to injection site) for up to 4 months. Spike is released from cells via the induction of exosomes, which are extracellular ~100nm sized vesicles used in cell-to-cell communication.
2/ “Results demonstrated induction of circulating exosomes expressing spike protein on day 14 after vaccination followed by Abs 14 d after the second dose.”
3/ “Exosomes with spike protein, Abs to SARS-CoV-2 spike, and T cells secreting IFN-γ and TNF-α increased following the booster dose.”
4/ “Transmission electron microscopy of exosomes also demonstrated spike protein Ags on their surface.”
5/ “Exosomes with spike protein and Abs decreased in parallel after four months.” (I would like to know the mechanism of how Spike protein is still present after 4 months).
6/ “These results demonstrate an important role of circulating exosomes with spike protein for effective immunization following mRNA-based vaccination.”
7/ Exosomes can also carry genetic information, such as RNA. Exosomes are known to be taken up by distant cells. Therefore, it’s possible that the mRNA from the vaccine could be shuttled to other tissues via the exosome transport pathway.
9/ a good primer on exosomes —> science.org/doi/10.1126/sc…

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More from @ScienceWDrDoug

21 Oct
1/ Does a large part of society really not understand why it’s a really bad idea to use mRNA or viral vector DNA to “vaccinate” someone who has natural immunity to COVID? Do people really not know what the immune system does to cells that express antigens on their surface?
2/ The immune system takes antigen-expressing cells out of commission via Cytotoxic T Cells (CD8+), Antibody-Dependent Cell-Mediated Cytotoxicity, and the Classical Pathway of the Complement System via Complement Dependent Lysis (CDL).
3/ Since mRNA lipid nanoparticles have access to many cell types via circulation, we have to assume that a great diversity of cells in different tissues become Spike-protein expressing factories. The spike protein on the surface of these cells targets them for immune attack.
Read 7 tweets
8 Oct
1/ Any fellow molecular biologists want to attempt answering this question: What is the probability that the tropism of the virus shifts due to vaccine-accelerated Spike evolution leading to binding of novel receptors other than ACE2?
2/ Since vaccine roll out, the Spike ORF has exhibited high mutation rates and entropy.
3/ If the structure of Spike shifts far enough away where it gains the ability to dock to another transmembrane protein (while maintaining proteolytic conversion via TMPRSS2 or other like protease), the virus could preferentially gain access to other cell/tissue types.
Read 6 tweets
7 Oct
1/ Vaccination Math = Let’s assuredly kill K% of people now and medically harm H% of people now because X% and Y% may (or may not) die and be harmed later.

To assess risk/reward, you need to know K, H, X, and Y. You also need a factor to account for the future “may or may not.”
2/ The factors that play into “may or may not” include modeling the herd immunity threshold (natural), viral evolution/attenuation rate, AND the adoption of current and new treatments, among other factors. We’ll call this factor “M”.
3/ Honest question: Do you think the powers that be did this type of math before pulling the trigger on the unprecedented campaign to vaccinate every person on the planet?
Read 6 tweets
6 Oct
1/ Myocarditis rates reported in VAERS were significantly higher in youths between the ages of 13 to 23 (p<0.0001) with ∼80% occurring in males. They found 19 times the expected number of myocarditis cases in the vaccination volunteers over background.
2/ In addition, a 5-fold increase in myocarditis rate was observed subsequent to dose 2 as opposed to dose 1 in 15-year-old males.
3/ Of the total myocarditis reports, 6 individuals died (1.1%) and of these, 2 were under 20 years of age - 1 was 13.
Read 6 tweets
5 Oct
1/ Them: Get vaccinated. It will stop infections and deaths.

Us: It doesn’t seem to be stopping infections all that much.

Them: Yeah, it’s called a breakthrough, and it’s rare.

Us: It doesn’t seem to be that rare.

Them: We never said it would stop infections, just deaths.
2/ Us: Well, the effectiveness of the vaccine to prevent death seems to be waning over time.

Them: Well we never said it would provide long-lasting protection. You need a booster.

Us: How often?

Them: We don’t know yet. Our science experts can’t seem to agree.
3/ Us: Ok, well let us know when you get all that worked out.

Them: No, you need to get vaccinated now or else.

Us: Well, what are the long term side effects?

Them: We don’t know. You can’t take VAERS data seriously. We have to wait until they analyze every report.
Read 4 tweets
4 Oct
1/ “Fully vaccinated were more likely than unvaccinated persons to be infected by variants carrying mutations associated with decreased antibody neutralization.”, and “In unvaccinated cases, most viruses consisted of non-resistant variants”
2/ In addition, the increase in the frequency of more antibody-resistant strains in the population correlates with the increase in the frequency of vaccination in the population
3/ “and the percentage of sequenced cases that were vaccine breakthroughs increased from 0% to 31.8% from February to June”
Read 8 tweets

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