Sorry Pfizer, maybe we don't need to order billions of vaccines more but thank you for your service.
Edit: this comment exploded, I was being sarcastic because Pfizer Ceo said confidently that we will all need frequent boosters like a good salesman would. And it's true that maybe it's prudent to buy boosters just in case.
If you don't mind the higher lethality and long-term damage of getting hospitalized with COVID-19 and then given ivermectin to try and cure yourself, sure.
I'd just get the vaccine and not get sick in the first place.
I did not know that, honestly quite surprised!
One thing to keep in consideration is that there is a very big evolutionary pressure for covid to get a mutation that bypasses the vaccine antibodies and still infect others, given that there are so many active infections still out there.
I now have good hope though!
To be fair humans are almost identical to chimpanzees biologically in many ways.
As long as the spike proteins tertiary structure has not changed to much from SARS to COVID, op could be correct. Emphasis on could.
> Next, we showed that patients (n = 23) who recovered from SARS (the disease associated with SARS-CoV infection) possess long-lasting memory T cells that are reactive to the N protein of SARS-CoV 17 years after the outbreak of SARS in 2003; these T cells displayed robust cross-reactivity to the N protein of SARS-CoV-2.
Thank you, seems to support OP's statement. Given that COVID antibody tests also show cross-reactivity with SARS it seems likely to me he is in fact correct.
Seconding the request for a source. The papers I've found say that SARS-1 survivors have antibodies that react to SARS-CoV-2 but don't neutralize the virus, and thus may not provide immunity.
So far the mRNA vaccines have shown strong effectiveness against the variants, but the others like AZ and the Chinese/Russian vaccines much less so. It's also worth noting that natural immunity is a somewhat random process (more random than the antibodies produced with vaccines) and not everyone develops the same level of protection.
This should be relatively easy to verify, we have millions of people who have been infected early last year so we can see how many of them got reinfected recently with one of the more recent strains.
If the immune response of the virus is close enough to what a vaccine gives and the mutation rate remains relatively constant, the number of reinfections would probably be a good indication of how much would we need subsequent shots, at least for a yearly renewal cycle.
The mRNA based technology underlying both the Pfizer and Moderna vaccines are expected to power a whole slew of applications in the future. I think these companies are quite happy that they just got an expedited, large scale demonstration of the effectiveness and safety of their tech, which will lead to many billions in future revenue.
I think you misunderstood, the GP is commenting on the Pfizer CEO saying that boosters will be required in 6 months which this paper seems to indicate won't be necessary.
No. The variants are variants, not strains. It's based on gene deletes primarily. More Sneaky just means a bit less effective. Studies suggest about half as effective. So from 90% to 80% etc still highly effective.
Most people in 1st world countries (where $20 is not that much) would, but I like that it might not be needed. It's less hassle, and it also breaks all the assumptions were made by the anti vaccine misinformation.
Anti-vax, anti-mask crowd have been so wrong so many times over the last year. I doubt another huge L would change their minds. It's twilight zone level stuff.
Alright. I mean on an individual level, I and I'm sure a large majority of people would take a single booster for improved safety from the variants that took this evolutionary path. All for like $20 (cost of a shot).
In case that you also had no idea what these cells do: they seem to be responsible for ensuring a long term immune response to the SARS-Cov2 pathogen, so the finding that patients who went through a Covid infection developed them is a good thing.
I still haven't seen anything about any infection-caused natural immunity involving anything other than the spike protein chosen for the mRNA vaccines.
Surely some people's immune system must be making antibodies targeting other features of the virus?
I know that might not make a practical difference at this point in terms of immunity, but it seems relevant to studies like these in terms of long-term, breadth vs depth immunity strategies that the body implements.
I don't remember where I read it or why exactly they did it, but I read this is already used to be able to test whether your antibodies come from natural infection or vaccination.
Those (spike protein) are the tests that are readily available, although they do have others that target other relatively stable portions of the virus. In fact the way that the "English'-B.1.1.7 and "South African" B.1.351 were originally discovered (before sequencing) was that they didn't replicate one of the PCR primers, but they are still targeting the functional element, which is required for replication/infection.
There are lots of things your body might respond to and even effectively fight off a COVID infection, it's just that not all of them are particularly stable. If you go to Nextstrain you can actually see which protein the different mutations are in (S is for spike). They're all over the place, but many change so much that you could have multiple strains within a single infection. RNA viruses are not very stable. Only the required functionality of the spike provides a relatively stable attack point.
More evidence that natural immunity to covid is the best form of immunity.
The responsible way to roll out the vaccination program would have been to test for covid antibodies first. Those with existing antibodies have no business taking an experimental vaccine they don't need.
>As controls, we also intracellularly stained PBMC from healthy volunteers 1 week after SARS-CoV-2 or seasonal influenza virus vaccination (Fig. 3a, Extended Data Fig. 1a-c). Consistent with the ELISpot data, low frequencies of S-binding BMPCs were detected in ten of the twelve convalescent specimens analyzed, but not in any of the nine control specimens(Fig. 3b).
My guess is that it'd be difficult to figure out what's a tracking URL and what's just a normal parameter.
Or maybe because HN is supposed to be minimalist: you upload something and know that people will see what you uploaded, unmarred by HN's modifications. I'm looking at you, Twitter.
The long tail of the distribution combined with the media’s search for interesting stories ensures that unlikely events will be featured more prominently in your observations of the world than they would deserve according to their probability alone.
I'm not an immunologist or even a biologist, but: biological lifeforms are complex things that don't really work in absolutes, but in shades of gray. Having antibodies and so on is not an absolute protection from reinfection, but rather helps fight it. If there aren't enough of them, or in various other circumstances (suppressed immune system, different virus variant, etc), it seems only natural that it is possible to be infected again.
> But then how does this explain that some people got covid twice?
DNA is really diverse and it will never be the case that _everyone_ responds identically to external stimuli. This is the problem with the "one size fits all" approach to drug and biologics development.
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[ 3.6 ms ] story [ 110 ms ] threadEdit: this comment exploded, I was being sarcastic because Pfizer Ceo said confidently that we will all need frequent boosters like a good salesman would. And it's true that maybe it's prudent to buy boosters just in case.
I'd just get the vaccine and not get sick in the first place.
Maybe for the synthetic immunity (who knows).
But in any case, SARS-1 and covid are about 80% similar. The "variants" of different covids are about 99.7% similar. Draw your own conclusions.
BTW people and chimpanzees share 99% of their DNA. We're basically the same, aren't we. /s
80% is not close at all, and 99.7% still can render a vaccine ineffective, of course the specifics matter.
> Next, we showed that patients (n = 23) who recovered from SARS (the disease associated with SARS-CoV infection) possess long-lasting memory T cells that are reactive to the N protein of SARS-CoV 17 years after the outbreak of SARS in 2003; these T cells displayed robust cross-reactivity to the N protein of SARS-CoV-2.
[0] https://pubmed.ncbi.nlm.nih.gov/32668444/
So far the mRNA vaccines have shown strong effectiveness against the variants, but the others like AZ and the Chinese/Russian vaccines much less so. It's also worth noting that natural immunity is a somewhat random process (more random than the antibodies produced with vaccines) and not everyone develops the same level of protection.
If the immune response of the virus is close enough to what a vaccine gives and the mutation rate remains relatively constant, the number of reinfections would probably be a good indication of how much would we need subsequent shots, at least for a yearly renewal cycle.
I wonder, are there any such studies?
https://www.popsci.com/story/health/hiv-vaccine-mrna-moderna...
Surely some people's immune system must be making antibodies targeting other features of the virus?
I know that might not make a practical difference at this point in terms of immunity, but it seems relevant to studies like these in terms of long-term, breadth vs depth immunity strategies that the body implements.
I don't remember where I read it or why exactly they did it, but I read this is already used to be able to test whether your antibodies come from natural infection or vaccination.
There are lots of things your body might respond to and even effectively fight off a COVID infection, it's just that not all of them are particularly stable. If you go to Nextstrain you can actually see which protein the different mutations are in (S is for spike). They're all over the place, but many change so much that you could have multiple strains within a single infection. RNA viruses are not very stable. Only the required functionality of the spike provides a relatively stable attack point.
spike (S), envelope (E), membrane (M), nucleocapsid (N)
https://nextstrain.org/ncov/global
The responsible way to roll out the vaccination program would have been to test for covid antibodies first. Those with existing antibodies have no business taking an experimental vaccine they don't need.
Or maybe because HN is supposed to be minimalist: you upload something and know that people will see what you uploaded, unmarred by HN's modifications. I'm looking at you, Twitter.
Now it is just pure commie propaganda.
Fucking liberal shits.
DNA is really diverse and it will never be the case that _everyone_ responds identically to external stimuli. This is the problem with the "one size fits all" approach to drug and biologics development.