Oops! New Peer Reviewed Published Study Shows That mRNA Injections Modifies Human DNA As Fast As Six Hours! We Were Told It Never Gets Into DNA!
A new peer reviewed study by Swedish researchers from Lund University published in the journal: Molecular Biology, shows that mRNA injections for COVID-19 by Pfizer reverse transcribes into human DNA in as little as six hours post-exposure! https://www.mdpi.com/1467-3045/44/3/73
We were told by these pharma giants and also fact checkers in the past that these COVID-19 injections will never get into our DNA, let alone modify it.
Do note however that Reuters CEO also sits on the board on Pfizer! https://www.pfizer.com/people/leadership/board-of-directors/james_smith
The Pfizer’s injections for COVID-19 has been one of the two most commonly used experimental pharma compound around the world in the current COVID-19 pandemic!
Lead author, Dr Markus Alden a professor at the department of clinical sciences at Lund University told Thailand Medical News,
“The safety profile of BNT162b2 is currently only available from short-term clinical studies. Less common adverse effects of BNT162b2 have been reported, including pericarditis, arrhythmia, deep-vein thrombosis, pulmonary embolism, myocardial infarction, intracranial hemorrhage, and thrombocytopenia.”
He added, “To better understand mechanisms underlying injection-related adverse effects, clinical investigations as well as cellular and molecular analyses are needed.”
The study team noted that a May of 2021 study by U.S. researchers had shown that SARS-CoV-2, the virus that causes COVID-19, could reverse transcribe into human DNA. https://www.thailandmedical.news/news/breaking-news-new-research-by-mit-and-nci-provides-further-evidence-of-controversial-claims-that-sars-cov-2-genes-can-integrate-with-human-dna
The study team questioned whether the same could happen with Pfizer’s COVID-19 injections, which uses messenger RNA instructions encapsulated in a manmade lipid nanoparticle to instruct human cells to manufacture the virus’s spike protein for the purpose of eliciting an immune response.
The study team said, “In this study, we aim to examine the effect of BNT162b2 on a human liver cell line in vitro and investigate if BNT162b2 can be reverse transcribed into DNA through endogenous mechanisms.”
The study team conducted in vitro
tests on a human liver cell line tagged Huh7 involving 0.5, 1, and 2 milligrams of BNT162b2 over a course of 6, 24, and 48 hours.
The study team explained their reasoning for the type of cell used and the dosages, “A previous study on mRNA injections against H10N8 and H7N9 influenza viruses using a similar LNP (lipid nanoparticle) delivery system showed that the mRNA injections can distribute rather nonspecifically to several organs such as liver, spleen, heart, kidney, lung, and brain, and the concentration in the liver is roughly 100 times lower than that of the intra-muscular injection site.”
The team added,“In the assessment report on BNT162b2 provided to EMA [European Medicines Agency] by Pfizer, the pharmacokinetic distribution studies in rats demonstrated that a relatively large proportion (up to 18%) of the total dose distributes to the liver.” https://www.ema.europa.eu/en/documents/assessment-report/comirnaty-epar-public-assessment-report_en.pdf
The study findings showed the detection of high levels of BNT162b2 in Huh7 cells and changes in gene expression of long interspersed nuclear element-1 (LINE-1), which is an endogenous reverse transcriptase.
It should be noted that a previous study has shown that entry of LINE-1 protein into the nucleus is associated with retrotransposition.” https://elifesciences.org/articles/30058
The study team further probed whether BNT162b2 is reversely transcribed into DNA when LINE-1 is elevated.
In order to do this, the study team purified the DNA in the Huh7 cell line that was exposed to the 0.5 mg dosage of BNT162b2 across all time frames, confirming Pfizer’s injection is reverse transcribed into human DNA as early as the 6-hour interval.
The study team warned, “Our study shows that BNT162b2 can be reverse transcribed to DNA in liver cell line Huh7, and this may give rise to the concern if BNT162b2-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects.”
The study team added, “At this stage, we do not know if DNA reverse transcribed from BNT162b2 is integrated into the cell genome. Further studies are needed to demonstrate the effect of BNT162b2 on genomic integrity, including whole genome sequencing of cells exposed to BNT162b2, as well as tissues from human subjects who received BNT162b2 injections.”
A very important previous study finding to note, produced by two Chinese scientists working at Sweden’s Umea University in October of 2021 found that both SARS-CoV-2 and the spike protein produced by injections was abundant in cellular nuclei and “inhibits DNA damage repair by hindering DNA repair protein recruitment.”
The study team concluded, “In the BNT162b2 toxicity report, no genotoxicity nor carcinogenicity studies have been provided. Our study shows that BNT162b2 can be reverse transcribed to DNA in liver cell line Huh7, and this may give rise to the concern if BNT162b2-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects. At this stage, we do not know if DNA reverse transcribed from BNT162b2 is integrated into the cell genome. Further urgent studies are needed to demonstrate the effect of BNT162b2 on genomic integrity, including whole genome sequencing of cells exposed to BNT162b2, as well as tissues from human subjects who received BNT162b2 injections.”
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