The COVID 💉 is comprised of mRNA encased in a lipid nanoparticle.
The mRNA is codon optimized with n1-methy-pseudoU and codes for a more durable spike protein.
It also contains dsDNA bacterial contaminants and an SV40 promoter.
See research of Kevin McKernan. >
PEG supports prolonged circulation of the LNPs, and their payload, the spike protein mRNA.
Spike protein is then expressed on the surface of cells in the endothelium all over the body.
This causes amyloid fibrin micro clots to form in response. See #TeamClots research >
The immune system reacts to the expression of the foreign spike protein, and in the process, damages the endothelial wall, releasing collagen.
The collagen and the PEG from the LNPs act like a Hemopatch™️ to strengthen the amyloid fibrin clots. This creates a durable matrix.
Dr Burkhardt's team published more autopsy data on COVID 💉 patients confirming lymphocytes in every organ; which means it's a good time to revisit this little gem of a paper, with many highly predictive statements about the LNPs in the #WarpedSpeed 💉>
Before we start it's interesting to note the paper is from a team at Thomas Jefferson University.
The same 🏫 which forced their president to publicly apologize for liking @AlexBerenson's tweets questioning the safety and efficiency of the 💉s.
The research looked at data showing the highly inflammatory nature of the lipid nanoparticles when tested in 🐁, injected into the muscle, and intranasally. > ncbi.nlm.nih.gov/pmc/articles/P…
They are dead because of the disastrous pandemic response directed by Fauci, who gave conflicting advice, censored life-saving early 💊s, and mandated lethal 🏥 protocols, in order to create fearful compliance and sell 💉💉💉. #FuckFauciFriday