All of CharlieMarr@protonmail.com's Comments + Replies

Thank you so much for your great answers.

I have one follow-up question for you.

I really liked/enjoyed your logic on why you decided to make your own vaccine.  You seem like a highly rational guy, and because of that, I find myself curious about your logic on the preceding decision--the decision that you would take a brand-new Covid-19 vaccine, and soon, from, say, Pfizer.  

Most people are eager to get that vaccine, but most people are not rationalists.  I'm curious about the logic an intelligent and skeptical rationalist used to decide he'd ... (read more)

2johnswentworth
I've been putting off answering this, because a proper answer would require diving into a lot of disparate evidence for some background models. But developments over the past few weeks have provided more direct data on the key assumption, so I can now point directly to that evidence rather than going through all the different pieces of weaker prior information. The key assumption underlying my belief (and, presumably, most other peoples' belief) in the efficacy of the commercial vaccines is that the data from the clinical trials is basically true and representative. If we believe the data, then the health risks are trivial (compared to COVID), and the effectiveness is decent, and our certainty about these two facts is very high. The vaccines are not "lightly tested" in any epistemically-relevant sense, only relative to the frankly-unnecessary extreme over-testing typically used. (Zvi's posts frequently provide helpful snapshots of the relevant data/analysis.) The question which you seem to be interested in is whether the data is trustworthy. The key model here is that, if there were anything even remotely suspicious in there, then regulators and the media would absolutely freak out over it. That's exactly what we've seen over the past few weeks - first with the AZ clotting thing, then with AZ calling their vaccine "79% effective" when the regulators thought it only merited "69 to 74% effective". The clotting thing in particular is a clear case where there was absolutely no real, important problem, and regulators/media freaked out over it anyway, because they are super-over-sensitive to even the tiniest hint of a problem. That follows directly from their incentives: regulators do not get punished for delaying good vaccines, but if a bad vaccine gets regulatory approval, then there's a scandal and an Official Investigation and "heads will roll".

How does the "vaccine design just isn't that hard" align with these points?

a) Average time to develop a vaccine for a new virus is many years

b) There is still no HIV vaccine after 35 years of well-funded research

c) Until a few months ago, there were no approved coronavirus vaccines for humans

I'm prepared to accept that "bureaucracy" is the main cause for the delays in standard big company vaccine development and approval.  

But if it's easy to develop vaccines, why has there been no coronavirus vaccine previously?  Why is there still no vaccine fo... (read more)

4johnswentworth
Good questions. First, I expect a disproportionate number of vaccine trials are for "unusually difficult" viruses, like HIV. After all, if it's an "easy" virus to make a vaccine for, then the first or second trial should work. It's only the "hard" viruses which require a large number of trials. I expect this is still mainly a result of regulatory hurdles. Clinical trials are slow and expensive, so there has to be a pretty big pot of gold at the end of the rainbow to make it happen. Also, companies tend to do what they already know how to do, so newer methods like mRNA or peptide vaccines usually require a big shock (like COVID) in order to see rapid adoption.

This seems like a cool and interesting experiment, and it seems rational from a "zoomed-in" perspective.  i.e. "if I'm going to get vaccinated, I might as well do it myself, nasally, with fewer ingredients....the potential benefits are greater than the costs.  Especially when considering adjacent benefits like learning, being a trailblazer, potentially advancing knowledge, etc."  

But if you "zoom out" and take a broader view of the whole Covid phenomenon, it seems like you may be (irrationally?) accepting a number of big assumptions before b... (read more)

2johnswentworth
At this point in the game, things like "advancing knowledge" and "I really want to know if it was actually this easy all along" are at least as big a factor as the object-level benefits. If this were last July, or if I lived in Europe, then it might be a different story, but at this point I'm likely to get vaccinated within a few months anyway. On your specific points: a) COVID still sucks, I don't want my food to taste like nothing for six months, etc, but I'm definitely not at any significant risk of death from COVID. b) I definitely do not expect that sleep/exercise/vitamin D/etc would achieve anywhere near the degree of risk reduction that a vaccine provides, and I do expect preventative to be way better than treatment here. c) I certainly would not consider "vaccine experts" reliable, as a category. I do think that I am extremely unusually good at distinguishing real experts from fake. Indeed, there's an argument to be made that this is the major thing which we should expect rationalists to be unusually good at. In the case of RadVac specifically, I think it is considerably more likely to work than a typical vaccine trial, and typical vaccine trials have ~40-50% success rates to start with (the highest success rate of any clinical trial category). d) Not sure what you mean by this one. Sounds like you're making a generalized efficient markets argument, but I'm not sure exactly what the argument is. e) Antibody test results would be the goal here. Though in practice, most governments seem so incompetent that they're not even actually looking at antibody test results or vaccination, so it's not a very large factor.