The Invasion of the Human Genetic Essence By Chris Knight (Florida)

Leading cardiologist and Covid vax critic  Peter A. McCullough has given a summary of recent scientific research that the mRNA spike protein from SARS-CoV-2 and not mRNA or adenoviral DNA entered the human cell nucleus. So, this is not exactly proof that the Covid vaxxes do the same, but makes it highly probable, given that the same spike protein is at work. We were told at the beginning of the Covid plandemic that the mRNA spike protein did not move from the deltoid injection site, but this was soon shown to be false. It was also said that Covid-19 did not integrate itself into the human nuclei, but that too seems to be false.  If it follows, and there needs to be more research done on this, that the mRNA spike protein from the Covid vaxxes, which produce more spikes than even the vax, do integrate into human cell nucleus, then there is a major problem for the human future, given that this is one of the most pathogenic and lethal proteins ever discovered, or engineered. It is perhaps no wonder then, that there are the adverse effects being seen in the vaxxed such as a rapid rise in cancers.

https://www.trialsitenews.com/a/sars-cov-2-spike-protein-found-in-the-human-nucleus-75dba3dd  

“In a recent paper by Sattar et al in collaboration with scientists from the National Institutes of Health (NIH), the authors report that both mRNA and Spike protein colocalized within the nucleus of human cells.[i] 

The authors note this is unusual and appears to not rely upon the furin cleavage site which is necessary for Spike protein entry into the cell. It is important to note the context and the methods of this paper utilized SARS-CoV-2 and not mRNA or adenoviral DNA vaccines. However, the ramifications of this finding cannot be understated. Having both one of the most pathogenic and lethal proteins ever discovered found within the nucleus of human cells with its genetic code is a hair-raising discovery. The paper was uploaded to the preprint server bioRxiv and still needs to be subjected to the peer review process.

A prior paper by Singh and Singh demonstrated Spike protein models anticipate an interaction with tumor suppressor genes P53 and BRCA1.[ii]  Sattar now says this could indeed happen!  Thus, Spike protein is at the scene of a potential crime—oncogenesis or the failure of immune surveillance against nascent cancer cells. Seneff et al have predicted that the Spike protein may be related to cell senescence and autophagy.[iii] 

This means more rapid aging of cells and then programmed cell death. I have had many patients ask me why they lose muscle mass and have hair loss after COVID-19 illness, these observations provide perhaps some explanatory basis for discussion at the cellular level.

Finally and most disturbing, Nunez-Castilla et al of demonstrated homology of the Spike protein with about three dozen other human proteins.[iv]   This explains why in the first place would the human nucleus allow entry of mRNA and Spike into the control center of the cell.  Could the genetic code of SARS-CoV-2 have been intentionally “humanized” as by design?

While Senator Rand Paul is doing a wonderful job staying focused on the possibility of U.S. government involvement in engineering of SARS-CoV-2 via the funding of gain-of-function research at the Wuhan Institute of Virology for example; more in-depth lines of inquiry are needed with preclinical-scientists and officials from Biomedical Advanced Research and Development Authority and the NIH to reveal how much they knew about mRNA, the Spike protein, and any risks to human cells during SARS-CoV-2 infection and over the longer term.

[i] Sattar S, Kabat J, Jerome K, Feldmann F, Bailey K, Mehedi M. Nuclear translocation of spike mRNA and protein is a novel pathogenic feature of SARS-CoV-2. bioRxiv [Preprint]. 2022 Sep 27:2022.09.27.509633. doi: 10.1101/2022.09.27.509633. PMID: 36203551; PMCID: PMC9536038.

[ii] Singh N, Bharara Singh A. S2 subunit of SARS-nCoV-2 interacts with tumor suppressor protein p53 and BRCA: an in silico study. Transl Oncol. 2020 Oct;13(10):100814. doi: 10.1016/j.tranon.2020.100814. Epub 2020 Jun 30. PMID: 32619819; PMCID: PMC7324311.

[iii] Seneff S, Nigh G, Kyriakopoulos AM, McCullough PA. Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs. Food Chem Toxicol. 2022 Jun;164:113008. doi: 10.1016/j.fct.2022.113008. Epub 2022 Apr 15. PMID: 35436552; PMCID: PMC9012513.

[iv] Nunez-Castilla J, Stebliankin V, Baral P, et al. Potential Autoimmunity Resulting from Molecular Mimicry between SARS-CoV-2 Spike and Human Proteins. Viruses. 2022;14(7):1415. Published 2022 Jun 28. doi:10.3390/v14071415”