You know what cracks me up? That there’s a rather high likelihood that I know more about mRNA that you do. Ignorance is bliss I suppose.
If you are aware of a specific mechanism that this kind of treatment can go poorly
Alright, so here’s one a concern.
As you’re certainly aware, there are studies that have found that viral RNA can carry into the host’s nucleus and be reverse-transcribed into the infected cell’s genome (for your convenience, here’s one such finding for SARS-CoV-2 https://doi.org/10.1073/pnas.2105968118), and that it produces chimeric transcripts that fuse the viral and host sequences.
Can you address how an mRNA vaccine would be able to ensure that such reverse transcription would not occur?
Here’s another concern.
The Pfizer BNT162b2 COVID vaccine is, of course, a lipid nanoparticle (LNP) mRNA vaccine, which is basically the approach discussed in the OP article. This article (Curr. Issues Mol. Biol. 2022, 44(3), 1115-1126) found that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure. Not only that, it has also found increased nuclear expression and distribution of LINE-1, an endogenous reverse transcriptase.
Since we previously covered the integration of foreign RNA into the host’s DNA, can you please explain how do you propose to identify and control for possible epigenetic effects of mRNA vaccines?
Seems like people found my zombie apocalypse parallel a bit too farfetched, but cancerous growth and tumors are in essence breakdowns of the genetic machinary in our cells, which mRNA vaccines are just too happy to mess with. All I’m advocating is more research, better understanding, and safety.
You know what cracks me up? That there’s a rather high likelihood that I know more about mRNA that you do. Ignorance is bliss I suppose.
Alright, so here’s one a concern.
As you’re certainly aware, there are studies that have found that viral RNA can carry into the host’s nucleus and be reverse-transcribed into the infected cell’s genome (for your convenience, here’s one such finding for SARS-CoV-2 https://doi.org/10.1073/pnas.2105968118), and that it produces chimeric transcripts that fuse the viral and host sequences.
Can you address how an mRNA vaccine would be able to ensure that such reverse transcription would not occur?
Here’s another concern.
The Pfizer BNT162b2 COVID vaccine is, of course, a lipid nanoparticle (LNP) mRNA vaccine, which is basically the approach discussed in the OP article. This article (Curr. Issues Mol. Biol. 2022, 44(3), 1115-1126) found that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure. Not only that, it has also found increased nuclear expression and distribution of LINE-1, an endogenous reverse transcriptase.
Since we previously covered the integration of foreign RNA into the host’s DNA, can you please explain how do you propose to identify and control for possible epigenetic effects of mRNA vaccines?
Seems like people found my zombie apocalypse parallel a bit too farfetched, but cancerous growth and tumors are in essence breakdowns of the genetic machinary in our cells, which mRNA vaccines are just too happy to mess with. All I’m advocating is more research, better understanding, and safety.