by Belle Carter, via DC Clothesline:
The mRNA used for Pfizer’s Wuhan coronavirus (COVID-19) vaccine disrupts cell repair mechanisms and allows SARS-CoV-2 spike proteins to alter a person’s DNA within six hours.
A February 2022 study done by researchers from Lund University in Sweden investigated the BNT162b2 vaccine’s effects on human cells, with a view to determining if its encoded spike protein RNA can be reverse-transcribed into human DNA. The aforementioned paper was published in Current Issues in Molecular Biology.
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The study findings revealed that the mRNA vaccine is able to enter the human liver cell line HuH7, with the shot’s mRNA transcribing into human DNA a mere six hours after exposure. Their in vitro study done on human liver cells was the first one of its kind. (Related: Study reveals Pfizer’s COVID-19 vaccine can potentially alter DNA in human liver cells.)
It echoed an October 2021 study published in Viruses, which found that spike protein infiltrates the cells’ nuclei and impairs the cell’s natural mechanism of repairing damaged DNA. The researchers from two universities in Sweden conducted their study in an artificial environment.
“Our findings provide evidence of the spike protein hijacking the DNA damage repair machinery and adaptive machinery in vitro. Although no evidence has been published that SARS-CoV-2 can infect thymocytes or bone marrow lymphoid cells, our in vitro V(D)J reporter assay shows that the spike protein intensely impeded V(D)J recombination,” the researchers wrote.
V(D)J recombination is the process by which T cells and B cells randomly assemble different gene segments – known as variable (V), diversity (D) and joining (J) genes – in order to generate unique receptors known as antigen receptors.
