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Reverse Transcription—Permanent Installation of mRNA Genetic Code
Unintended Consequence of Novel COVID-19 Vaccines
When we heard about Operation Warp Speed there was sense of shock and awe. American greatness was poised to strike the “China Virus” and it was going to be defeated in a matter of weeks. The Defense Advanced Research Projects Agency (DARPA) created a project many years ago called ADEPT Pandemic Prevention Platform (P3) whose stated goal was to “end pandemics in 60 days with mRNA technology.”[i] Our government has had a love affair with mRNA for over a decade for precisely a time such as the SARS-CoV-2 outbreak. Hardly a virus from China, we have learned that Dr. Ralph Baric at the University of North Carolina in Chapel Hill has been publishing on coronaviruses since the 1990’s. Baric and his consortium including Harvard and two Swiss labs conceived the projects, wrote the federal grants, and once awarded, did their development work in the Wuhan Institute of Virology biosecurity annex level 4. The laboratory built by Stephane Bancel formerly at BioMérieux and now CEO of Moderna, the NIH partner in the mRNA patent.[ii] I wonder in all the DARPA and NIH meetings that occurred in the last ten years on mRNA, did they ever consider reverse transcription? If the mRNA stays long enough in the cytosol and is not dissolved by enzymes, the human cell could find base pairs of nucleic acids and create a mirror image of the genetic code which could be brought into the nucleus of the cell for insertion into the human genome. This is such a giant consideration because genetic code for a damaging and lethal protein installed into our own cells permanently would be passed down to somatic daughter cells and from spermatocytes and oocytes to an embryo. Forever changing the human genome for future generations must have been a large part of the safety discussion in those DARPA and NIH transcripts—only investigation and release of documents will tell the story. In the meantime, Alden et al have demonstrated integration of the center 444 base pair amplicon or reporter region from the Pfizer vaccine into the human nucleus in a hepatoma cell line.[iii] This paper has not been challenged by any credible authority nor disproven by any other experiments.
Kyriakopoulos et al (including Dr. McCullough) have illustrated what the ramifications would be for those cells that have been permanently installed with Pfizer or Moderna genetic code.[iv] In addition to the nine well recognized effects of the Spike protein in the human body, one of the potential consequences is oncogenesis. By suppression of the natural tumor surveillance system(s) in even one cell, it is conceivable that reverse transcription could lead to cancer with a single ill-advised injection of mRNA if it was delivered to a cancer-prone cell line in a susceptible person.
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At this time, it is fair to say reverse transcription of mRNA into the human genome is still theoretical. But it should be clear that more studies by independent laboratories should be funded immediately. The implications given the massive numbers of recipients are simply too large to ignore this long-term safety concern. So the next time you see your doctor, ask him or her if they took an mRNA vaccine. When they say yes, ask them if the considered reverse transcription when the needle plunged into the arm. Did they ever think they would be changed permanently? When brushed aside with “the CDC says mRNA does not change the human genome” then forward this issue of Courageous Discourse and suggest a life-altering a five-minute read.
[i] Dr. Amy Jenkins, Pandemic Prevention Platform (P3), DARPA, P3 focuses on rapid discovery, characterization, production, testing, and delivery of efficacious DNA- and RNA-encoded medical countermeasures, a foundational technology pioneered by DARPA under the Autonomous Diagnostics to Enable Prevention and Therapeutics (ADEPT) program that provides the body with instructions on how to immediately begin producing protective antibodies against a given threat.
[iii] Aldén, M.; Olofsson Falla, F.; Yang, D.; Barghouth, M.; Luan, C.; Rasmussen, M.; De Marinis, Y. Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line. Curr. Issues Mol. Biol. 2022, 44, 1115-1126. https://doi.org/10.3390/cimb44030073
[iv] Anthony M. Kyriakopoulos, Peter A. McCullough, Greg Nigh and Stephanie Seneff* Potential Mechanisms for Human Genome Integration of Genetic Code from SARS-CoV-2 mRNA Vaccination: Implications for Disease. Neurological Disorders ISSN: 2329-6895