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There are plenty of shortcuts in medicine. Think how you would stop this strain from being spread by individuals once it was identified. This strain will spread no matter what the FDA says.

Personally I think the regulatory authorities would rapid approve it based on the epidemiology data collected in the process of finding the strain. The FDA has already shown that it can move faster than its usual glacial pace given sufficient motivation.

The much more important question is when are we going to start seriously looking for such a strain?




I don’t see that any regulatory authority would approve something that is capable of spreading, regardless of the possible benefits: it would violate medical ethics. Reread the Belmont Report.

There are many teams all over the world that are looking for less deadly (and more deadly!) strains to guide development of therapies. They’re too busy right now to post on message boards or speak to reporters. It’s however extremely unlikely that a less deadly strain will become the therapy, although it could be the basis of a therapy (but I think this too is unlikely).


All the attenuated live viral vaccines spread. This is one of the reasons they are so effective since they keep herd immunity up. For example, every kid that gets the live polio vaccine spreads it around to their peers and parents.


> All the attenuated live viral vaccines spread.

Can you point me to sources supporting that claim? I searched myself, and what I found says that our knowledge is limited to the polio vaccine:

"Little attention has been given to vaccine transmission, possibly because transmission is rarely measured and largely unknown in humans except for the oral polio vaccine. Whether transmission is indeed rare for other live vaccines, or has merely gone unnoticed, is not clear – polio vaccine transmission is accompanied by evolution to high virulence, creating problems that draw attention to transmission."

From "Transmissible Viral Vaccines", James J. Bull et al., Trends in Microbiology, January 2018. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777272/


This is a difficult topic to research these days due to the anti-vax/anti-anti-vax noise. :(

It doesn’t appear that horizontal transfer is absurd, and while I’m not immediately seeing a large body of evidence that it happens all the time, it does seem to be generally accepted that it occurs.

Here’s what I believe to be an informative article on the topic: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667938/


That’s a bug, not a feature: the OPV went to bivalent a few years ago to reduce the odds of vaccine-related cases.


Well your bug is a feature.

The polio vaccine actually went to the inactive form to reduce the risk of polio from one of the vaccine strains reverting to wild type and infecting others. It is still less effective at achieving herd immunity than the live version because of the lack of viral spread.


[flagged]



I am sure all the kids that got polio from someone else vaccine are glad to know this.


It hurts your case if you respond defensively or sarcastically.


Yes :(


Don't be hard on yourself; it happens. It's hard to withstand hours of engagement with internet commenters. The worst comments make a much deeper impression than everything else, just as getting stung by a bee is more memorable than seeing a butterfly.


Serious question: are we not? People are sequencing these things like crazy (c.f. the nextstrain.org data). Epidemiologists are working like mad to come up with data on severity in regions all over the globe. Virologists everywhere are dropping what they're doing otherwise to work on covid.

It sorta strains reason to argue that none of these people thought of looking for an attenuated strain.

Isn't the simpler truth just that finding one takes a lot of ground work that's already being done, but hasn't born fruit yet?


The sequencing is not the important thing here, but the search for strains with gene deletions and contact tracing everyone in the area to find more cases to prove the strain is attenuated. As far as I know nobody is doing this.


You’re fairly hard to get in contact with directly. Would you mind sending me an email? I don’t think I’ll be a your “middle hop”, but I’ll try. My email is lyndsy@<my_HN_username>.com

My username here is my real name, and I should be easy to find. It’s also my username on Twitter, Keybase, and most other popular platforms.


From the update section of the original post:

> If you think you might be that first hop person then please get in contact with me at daniel.tillett@gmail.com


Thank you. I don’t know if that just wasn’t there when I posted, or if I just missed it, but I appreciate it.


It was there, but I put it right at the bottom so at least only people who read the entire post would find it. I am at least a lot easier to get in contact with than anyone with the political clout to make this happen.


they re probably not sequencing asymptomatic people's virus, it would require some specific expedition. it doesn't even sound hard or expensive

reply to @ajross:

how would they know someone is asymptomatic? afaik they are mostly testing people who have symptoms , and their contacts (who will have contracted the same , symptomatic strain)

I think in germany they did antibody testing, or PCR of swabs of people who mostly no longer had a live virus infection to sequence. also, it seems the idea has merit; and i havent read about any team looking for this specific method (identify gene deletions and tracing). It certainly doesn't hurt (and doesnt cost much) to try

btw sweden is doing a survey of live infections in stockholm, however i don't think that they sequence the viruses

to @danieltillet:

maybe post about it in reddit on r/covid19, some epidemiologists hang out there for the latest news


It is not hard to do the sequencing to find candidate attenuated strains (you are just looking for strains with deletions in key genes). The more difficult part is all the contact tracing in the area around where the strain is first found to check if the strain really is attenuated.

The ideal outcome is you find a strain with a deletion and you then test everyone in the area and you find 10,000 more people infected with the strain that have only a mild case and none of these people are in the hospitals. This strain would be very valuable to have.


Are they not? That seems like a pretty obvious experiment to do.

For reference: I have a family member in virology. He reports that everyone he knows is now working on covid, mostly because if they don't they can't come to work on anything. The biggest problem is finding subjects that will produce a paper of any kind. I really don't think research bandwidth is the issue here.

I guess I have to repeat the question as its converse: is there any evidence that this is not happening? If it isn't, let's figure out the right people to pressure and not just discuss it on HN. And if it is, maybe we should let the experts do their work without pretending to have had their ideas for them?


If you know anyone working on my idea please let me know as I will update my blog post. Nothing would please me more than to learn that someone is already doing this on a serious level.


> how would they know someone is asymptomatic? afaik they are mostly testing people who have symptoms

There was literally a paper published yesterday (or the day before) on a blanket screen done on a population in germany to get some data on the undercount of asymptomatic cases. It was front page news on all the mainstream news sites...

I gotta be honest. This whole discussion has an "amateur hour" vibe. I have a hard time believing that professional academics in a long-established and very competetive field really failed to remember how the measles vaccine worked.

It's not that I think this is a bad idea, just that (1) it's almost certainly someone else's idea already, (2) is therefore probably harder to do than presented and (3) is thus not the magic bullet people are looking for.

To wit: stay the fuck home. Maybe someone will save us. They probably won't. We beat this with isolation or we wait for a vaccine.


I think what you are missing here is what is the novel part of my idea and what is the conventional. It is not novel to think of an attenuated vaccine, what is novel is to look for an attenuated strain in a pandemic using genome sequencing. I hope someone else has thought of this, but so far I haven’t seen any evidence of this.

Waiting for vaccine is not a good option. This is a situation with only hard choices.


Why else are hundreds of different labs around the world genome sequencing?


To assess the diversity and spread of the virus it appears. To the best of my knowledge nobody is systematically looking for a natural attenuated strain by genome sequencing. If you are then please get in contact with me.


"Waiting for a vaccine" is mostly a strawman. We're being asked to wait 2-3 months for the outbreaks to reach a size where they can be contained by testing, tracing and quarantine. But that only works if people take this seriously and honor the lockdowns.


Even if this would work in rich countries, this is not a realistic option for people in poor countries. They do not have the money to wait in isolation for the next 3 months.


We’re also likely to see convalescent sera available shortly, and neutralizing antibodies available in several months. Those, along with more widely available testing, will help us tread water until we develop a good drug or vaccine.




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