This was a great summary posted on the raccoon (coon)\u00a0 server:<\/p>\n
Got a relay message of Darl to that : Half of the nsp\u2019s and orf\u2019s in sars covid-2 block interferon , so the virus can replicate quicker without the first line of defence. In the mRNA , they have modified nucleotides, vaccinia capping enzymes , optimised codons gp 120 and lnp \u2018s which also block interferon. mRNA cannot get into cells without degradation, without blocking interferon. mRNA is extremely fragile to degradation, hence decades of failures. Warren and karoka, found that by the use of b18r and pseudouridine, they could finally stabilise the mRNA into cells. - Due to blocking interferon in mRNA b cells do not have a turn off switch. Excessive b cells is the issue with autoimmunity with igg4 . Every system in the body is affected. With igg4 we see a case of fibrous tendrils in the vascular system , which are not breaking down, this can affect all organs. Interferon protects the bbb , without it the virus and mRNA gets into the cns also Cancer relies on an intact interferon to recognise cell multiplication. It notifies nk cells to kill multiplying cells. Next step macrophage\u2019s clean up the dead cells, buuuuut macrophages are encouraged by interferon also , so no cell death and no debris clean up . Interferon manages bacterial infections, without it bacterial infections blossomed , often as a secondary infection, so antibiotics weren\u2019t used in covid as everyone said they don\u2019t work on viruses, incorrect, bacterial secondary infection. In effect we are look at immunodeficiency syndrome, our innate and adaptive immune systems have been aborted<\/pre>\nSomeone had the idea to run a “fact check” on it by running it through A.I. and it turns out it is correct.<\/p>\n
Brief Summary of the Dangerous Mechanisms of Vax Spike Proteins<\/a><\/p><\/blockquote>\n