One of the troubling philosophical and medical ethics issues, beyond Covid vax injuries, is the integration of the mRNA vaccine into human DNA. That prospect was denied in the early part of the vaccine rollout, but more recently scientific evidence has accumulated indicating that there is indeed an integration of the mRNA into human liver cells, at least shown in a test tube experiment. That is not a mere biological curiosity, since it is a landmark philosophical change, for the human genome is now essentially altered by the vax.

We have covered the idea of transhumanism, the philosophy of the World Economic Forum. Could it be that they saw the Covid plandemic as a way of making the first stage of the transformation of human nature? In my opinion, this is truly Satanic. The ramifications, from an ethical and theological position are profound, and in many respects, there is a parallel to the Mark of the Beast of Revelation 13: 16. It is far from certain where this will go.

https://www.trialsitenews.com/a/covid-19-mrna-vaccines-may-integrate-into-the-human-genome-8295eff9

“New research has illuminated the mechanisms of potential mRNA vaccine integration into genes. This research adds to the ongoing debate about whether mRNA vaccines can alter human DNA. In an effort to curb the uncontrollable spread of SARS-CoV-2, mRNA vaccines were broadly administered to the global population. Though mRNA technology enabled the quick development and deployment of the much-needed vaccines, its long-term safety is now at the forefront of concern. 

COVID-19 spread globally at an unprecedented rate. Governments and public health agencies were not adequately prepared to battle a highly contagious, infectious, and spreadable viral pathogen. While SARS-CoV-2 behaves similarly to known influenza viruses, existing vaccines were not equipped to induce immunity against it, since the viral structures and molecular interactions are so different. The development of a new vaccine became a top priority, necessitating a short timeline to save as many lives as possible.”

https://www.mdpi.com/1467-3045/44/3/73/htm

Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line

Curr. Issues Mol. Biol. 2022, 44(3), 1115-1126; https://doi.org/10.3390/cimb44030073

Preclinical studies of COVID-19 mRNA vaccine BNT162b2, developed by Pfizer and BioNTech, showed reversible hepatic effects in animals that received the BNT162b2 injection. Furthermore, a recent study showed that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of human cells. In this study, we investigated the effect of BNT162b2 on the human liver cell line Huh7 in vitro. Huh7 cells were exposed to BNT162b2, and quantitative PCR was performed on RNA extracted from the cells. We detected 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. Immunohistochemistry using antibody binding to LINE-1 open reading frame-1 RNA-binding protein (ORFp1) on Huh7 cells treated with BNT162b2 indicated increased nucleus distribution of LINE-1. PCR on genomic DNA of Huh7 cells exposed to BNT162b2 amplified the DNA sequence unique to BNT162b2. Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure.

https://www.trialsitenews.com/a/reverse-transcriptionpermanent-installation-of-mrna-genetic-code-d49ae601

“Should we be concerned about potential unintended consequences of novel, mRNA-based COVID-19 vaccines? When we heard about Operation Warp Speed, there was a 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. Likely not a virus from China, at least not originally, 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 was 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.”