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Comment by ceejayoz | Hacker News Reader

A reminder that anyone can be a "Forbes contributor" (https://www.niemanlab.org/2022/02/an-incomplete-history-of-f...), and "reportedly" is thrown in there with zero evidence.

It's highly unlikely the booster trials were on eight mice.

edit: Found the source of the eight mouse thing; it's a misreading of https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-..., page 21. It's not the safety trial, it's the immunogenicity comparison on a small population of older mice previously given the primary vaccine. (The previous slide, #20, has a heading of "Pre-Clinical Studies"; #21 is describing the early studies before the human trials.)

Page six debunks the idea it's only been tested on mice entirely; it cites a trial of 512 human adults for the Moderna BA.4/BA.5 Omicron booster.

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Page six labels the 512 BA.4/BA.5 test as "Part H"

> Part H enrolled Aug 10-23, 2022

These people entered the study less than a month ago?

https://www.npr.org/sections/health-shots/2022/08/18/1117778...

A month is more than enough to demonstrate safety; vaccine reactions to the original shot (and in general) were all rapid.

As that article notes, flu shots have a similar regulatory regime:

> And some scientists say health officials know enough about how vaccines work to start handling the COVID-19 vaccines like the flu vaccines, which are changed every year to try to match whatever strains are likely to be circulating but aren't routinely tested again every year.

and that the new vaccine still expresses the original proteins the already-approved vaccinations were expressing; in the worst-case scenario that mice and humans react similarly to Alpha/Delta but wildly differently to Omicron/BA.4/BA.5, we're still likely generating the at least the original immune response:

> The new booster will be identical to the original vaccines except it will contain genetic coding for two versions of the protein the virus uses to infect cells — the protein from the original vaccine and proteins from the BA.4 and BA.5 omicron subvariants.

A rapid approval process is going to be important for boosters, for the same reasons it is in flu shots. It's very clear the claim that it was only tested on eight mice is false.

The FDA extended the EUA to include BA.4/BA.5 boosters on August 31, which was 1-2 weeks after those people entered the study.

This is because the ba.4/ba.5 vaccine is so incredibly close to the ba.1 bivalent vaccine, which did see more human trials and showed a similar safety profile as the original vaccine.

Kinda like how we get a new flu vaccine every year that doesn't go through a years long clinical study

(Edit to fix a typo)

Sounds like conjecture to me. But that’s fine, I understand the argument for printing new mRNA vaccines. But please don’t force me to take it to keep my job or travel internationally, and don’t call me an anti-vaxxer for refusing to inject myself with an experimental vaccine that’s been tested in eight mice and a small group of humans for two weeks.

I'm not saying you have to get it. I'd like everyone to get the vaccine, because it is showing greatly improved outcomes over pre vaccine COVID.

You are anti this vaccine, and your posture is largely fear based rather than scientifically consistent given your not-an-anti-vaxxer self probably gets every year

>A month is more than enough to demonstrate safety; vaccine reactions to the original shot (and in general) were all rapid.

You see the tautology here, right?

No; vaccines continue to be monitored. We still keep track of safety events on vaccines that have been around for decades.

Many years of experience with vaccination gives us useful info on how bodies react to them, which allows us to approve vaccines based on logical criteria.

You're (intentionally?) missing the point, which is that long-term effects could not have been sufficiently monitored at the time they were thrust upon the general population.

It is possible to believe the vaccines are safe, and to support their use, while still conceding this point.

> which is that long-term effects could not have been sufficiently monitored at the time they were thrust upon the general population

Sure, that'd require a time machine. Thus, we're left going "hey, what happened with every other vaccination we've ever done?" and making decisions based on that wealth of information.

People attempting to make this point like to pretend the same isn't true for not getting the vaccine. What's the long-term effect of unvaccinated people getting COVID? Do we have a 20 year safety study on going unvaccinated in this pandemic?

>Thus, we're left going "hey, what happened with every other vaccination we've ever done?" and making decisions based on that wealth of information.

Now you're being disingenuous. There is another approach, and it is the one traditionally endorsed by the medical profession: prudence.

Put plainly: the deontologically correct way of proceeding would have been to say "we don't know enough to assert the vaccines are safe", and not thrust them onto an unwilling public.

>Do we have a 20 year safety study on going unvaccinated in this pandemic?

No. This is why I am not arguing against vaccines. I am arguing against mandates.

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