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Culture War Roundup for the week of January 2, 2023

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From wikipedia- "SARS‑CoV‑2 is a positive-sense single-stranded RNA virus[14] that is contagious in humans.[15]". Specifically, it enters your cell, expresses a RNA dependent RNA polymerase to copy its RNA, and then the RNA is translated into proteins that, with the genome, form new RNA viruses that go on to infect more cells. This means that, like the vaccines, covid itself puts RNA into your cells to replicate itself. So that doesn't make the vaccine any worse than covid. Or any one of the hundreds of respiratory viruses that float around, hundreds of which you've been infected with. And the RNA itself from the vaccine is just a (slightly modified) spike protein RNA from the original coronavirus.

By this standard, plenty of previous vaccines are gene therapy - weakened live virus, adenovirus vector, etc.

We know the certain viruses like HIV are able to insert their genomes of RNA into the human genome but only after they have converted it into DNA. This is accomplished via a virus enzyme called reverse transcriptase – an enzyme humans don't have. So the upshot is we don't have a way for mRNA vaccines to be inserted into our genomes. SO current vaccines are safe.

Yeah, lots of viruses do this. Covid is much less likely to, because it doesn't have DNA as part of its lifecycle, and doesn't encode a reverse transcriptase to make more viral DNA.

this is just a case of 'not understanding what you are talking about'.

Not that I claim to fully understand what I'm talking about (IANAB), but IIRC the difference is that a COVID infection specifically targets a subset of cell-types in your respiratory system -- the vaccine is in your blood and spreads all over the place, entering many types of cells and causing them to produce spike protein.

This seems like quite a different mechanism -- doesn't mean it's not safe, but it introduces a number of unknowns.

The virus is also going to be in your blood and spreading everywhere.

Sure, but AIUI it can only replicate in cells with ACE-2 receptors -- which is different from the mRNA vaccines, right?

ACE2 receptors are very widespread, though.

Are they as widespread as cells which can be hijacked by the mRNA vaccines, though? (Or infected by adenoviruses, for that matter)

I don't know, but I'm pretty sure they are different.

Which introduces unknowns.

Which is all that I'm saying.

At a glance I couldn't find anything in particular for the COVID vaccines, but the delivery system used for the mRNA vaccines are lipid nanoparticles, which have been in use for a short while, and can be targeted towards certain cells. (Some newfangled cancer vaccines, for example, use targeted lipid nanoparticles.)

So I'm not sure about whether they would be as widespread as COVID-susceptible cells, but based on the mechanism of uptake - which has nothing to do with the mRNA - it seems to be a technology that can be used for targeted cell uptake of drug/vaccine/etc.

They would probably be different cells, though, yes, though because the vaccines wouldn't replicate like viruses do, I would expect the distribution of uptake to be more local than with a COVID infection.

Not sure what you're getting at with adenoviruses, but it would probably depend on which? Most human adenoviruses would attach to CAR, which I'm pretty sure is widespread but not exactly everywhere, or CD46, which actually is everywhere.

At a glance I couldn't find anything in particular for the COVID vaccines, but the delivery system used for the mRNA vaccines are lipid nanoparticles, which have been in use for a short while, and can be targeted towards certain cells. (Some newfangled cancer vaccines, for example, use targeted lipid nanoparticles.)

So I'm not sure about whether they would be as widespread as COVID-susceptible cells, but based on the mechanism of uptake - which has nothing to do with the mRNA - it seems to be a technology that can be used for targeted cell uptake of drug/vaccine/etc.

In other words, you don't know either.

Not sure what you're getting at with adenoviruses

The other major spike protein delivery vector used in (Western) vaccines was a chimpanzee adenovirus. That was Astrazenica and Johnson & Johnson I believe.

In other words, you don't know either.

Indeed, but based on how it has been used before we can make an educated guess that it was probably not all cells, and probably more likely than not a subset of cells more restrictive than “cells with ACE2 receptor”. Are we really practicing radical skepticism here?

In any case, it‘s likely to get to fewer cells and stay more local than a virus would, given that it doesn’t replicate.

And it rather should dampen your worry (at least re:vaccine vs virus) here:

Not that I claim to fully understand what I'm talking about (IANAB), but IIRC the difference is that a COVID infection specifically targets a subset of cell-types in your respiratory system -- the vaccine is in your blood and spreads all over the place, entering many types of cells and causing them to produce spike protein.

Since COVID is in your blood and spreads all over the place too.

The other major spike protein delivery vector used in (Western) vaccines was a chimpanzee adenovirus. That was Astrazenica and Johnson & Johnson I believe.

Ah, the vector-based vaccines. I didn‘t read up much on them unfortunately.

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