CV19. spike can become integrated in your DNA; spike is in mRNA vaccine
Here’s a very important scientific article about how the spike protein, the thing used in the mRNA vaccines, can imbed itself in the DNA via reverse transcriptase of CV patients. The patients who recovered will still test positive and are thought to shed virus due to this.
The official story is that normal mRNA naturally degrades post transcription in cytoplasm, so “of course the vaccine will too.” Not so fast…they stabilized the mRNA in the vaccine. So when does vaccine mRNA degrade? We don’t know. Remember the 2012 gain of function study done at UNC Chapel Hill was specifically about inserting this spike into SARS. It made it capable of penetrating both animal and human cells easily, and did not respond to any conventional treatment.
The spike is the causative agent of the lung fibrosis since it embeds and is replicated endlessly.
This study completed in Dec. 2020, has been in literary purgatory awaiting peer review before publication. This is the pre-version available electronically. My bet is that it will never be reviewed.
SARS-CoV-2 RNA reverse-transcribed and integrated into the human genome
Prolonged SARS-CoV-2 RNA shedding and recurrence of PCR-positive tests have been widely reported in patients after recovery, yet these patients most commonly are non-infectious. Here we investigated the possibility that SARS-CoV-2 RNAs can be reverse-transcribed and integrated into the human genome and that transcription of the integrated sequences might account for PCR-positive tests. In support of this hypothesis, we found chimeric transcripts consisting of viral fused to cellular sequences in published data sets of SARS-CoV-2 infected cultured cells and primary cells of patients, consistent with the transcription of viral sequences integrated into the genome. To experimentally corroborate the possibility of viral retro-integration, we describe evidence that SARS-CoV-2 RNAs can be reverse transcribed in human cells by reverse transcriptase (RT) from LINE-1 elements or by HIV-1 RT, and that these DNA sequences can be integrated into the cell genome and subsequently be transcribed. Human endogenous LINE-1 expression was induced upon SARS-CoV-2 infection or by cytokine exposure in cultured cells, suggesting a molecular mechanism for SARS-CoV-2 retro-integration in patients. This novel feature of SARS-CoV-2 infection may explain why patients can continue to produce viral RNA after recovery and suggests a new aspect of RNA virus replication.
Yes, looking forward to Chris’ next Covid19 webcast.
If it can insert into the human genome, we need to understand if that is only somatic cells or also germ cells.
What does that imply? Are we talking about long term illness/health issues being triggered by that spike?
Looks like three main points:
1) integrating foreign RNA into the “LINE-1” section of DNA could be a form of long-lived immune system stimulant. “Lookie here: this is what you wanna kill.”
2) It might – alternatively – cause the cytokine storm.
[i.e. the authors really don’t know which is true]
3) PCR tests structured to look for this RNA section could be set off by the bits that got integrated into these LINE-1 sections of our DNA. So we can “test positive” for a long, long time even with no live virus inside.
We are definitely seeing #3 for sure.
From an evolutionary perspective, retro-integration of viral RNA by LINE-1 could be an adaptive response by the host to provide sustaining antigen expression possibly enhancing protective immunity. Conversely, retro-integration of viral RNAs could be detrimental and cause a more severe immune response in patients such as a “cytokine storm” or auto-immune reactions.
The reliance of PCR tests to assess the effect of treatments on viral replication and viral load may not reflect the efficacy of the treatment to suppress viral replication as the PCR assay may detect viral transcripts from viral sequences stably integrated into the genome rather than infectious virus.
Well Damn Hohhot. What a find.
I was thinking that all of the “gene therapy” talk was hyperbole. But maybe not!
to my knowledge, we don’t actually know with certainty what is in the lipid nano-particles coated in PEG.
it is proprietary information.
and THIS vaccine may not be the actual goal. Perhaps it paves the way (see these vaccines are safe) for a he next series of vaccines which deliver the intended modifications.
we just don’t know.
time to re watch I Am Legend.
For the last 10 days, or so, I am seeing that in my rural county of approx. 7000, jabs have not increased. No change from 2,126. I am waiting for early to mid May to see if this picks up, indicating people getting the second jab. We originally had just Pfizer and J&J. I don’t know if J&J is still paused in my state.
If you want to know why they stopped the Johnson and Johnson vaccines here is your answer.
The media tells you of “blood clots” but that doesn’t really convey what is happening.
>>> The media tells you of “blood clots” but that doesn’t really convey what is happening.
I think my sister in law’s father can help with that.
He got a blood clot in the vein that drains his left eye, about 20 years ago.
Nobody realized it was a clot. That part took about 9 months.
His eye swelled up about the size of a golf ball, and then I didn’t see him for a while.
From what I hear, it got bigger. He had to wear a stainless “bra” for his eye to keep it from falling out or dangling around his face.
Eventually they did a surgical “roto rooter” operation by sending a tool in through his thigh, up the circulatory system to his forehead.
His eye was almost instantly back to normal.
Watching him go through that, was enough to make me REALLY fear blood clots.
Not just an issue with J&J-
Thailand is using Chinese Sinovac. 7 people partially paralyzed.