2/ That includes USA, Latin Amer, and South Africa study sites. It will be important to see more data, because the initial press release was definitely thin on data. But, initial report 72% efficacy against "moderate to severe" disease. That is good for a single dose immunization
3/ The J&J COVID-19 vaccine generated good immune responses in people after one immunization, but there was a substantial boost to the antibody response after a 2nd immunization. A 4x gain. (T cell responses after the 2nd dose were not reported) nejm.org/doi/10.1056/NE…
4/ So, it is reasonable to expect that a two dose regimen of the J&J COVID vaccine would have significantly higher protection than the one dose. Again, good news.
5/ Probably most notably, they reported "72% in the United States and 57% in South Africa [SA]." In SA, almost all cases now are the "SA variant" (aka 501Y.V2), which has significant evidence of partial immune escape.
6/ (Other people have covered this variant topic extensively, and I will try to make some comments and re-tweet others later today.) One key concern has been whether vaccines would still protect against this SA variant.
7/ A 15% drop in efficacy between "regular" SARS2 and the SA variant (i.e., US clinical trial and SA trial), is actually good news. That is a rather moderate change in efficacy. And, again, this was a single dose of J&J.
8/ That vaccine efficacy of J&J 1-dose against "regular" vs. SA variant is consistent with either:
(i) A decrease in potency of antibodies against the SA variant is modest for J&J vaccine.
(ii) The T cell responses by the J&J vaccine play a big role in protection.
or
9/
(iii) the 'cross protection' against the SA variant is restricted to protection against more serious COVID.
There is no specific data for each of those 3 options. It will be important to get more information on each.
10/ Option 1 would be consistent with recent pre-prints on neutralizing antibody titers in Moderna or Pfizer vaccinees being moderately lower against the SA variant or similar mutants.
11/ Option 2 would be consistent with a range of correlative data indicating CD4 and CD8 T cells have protective roles in COVID-19 (summarized in the review below). doi.org/10.1016/j.cell…
12/ Also note that the J&J vaccine clinical trials were done during periods of extremely high SARS2 transmission in American and South Africa, with lots of virus around. So (as noted for the Novavax UK result), that is a tough environment for vaccine efficacy.
13/ (i.e., most likely a higher bar for protection than summer transmission in the USA, or anywhere with low level SARS2 transmission).
14/ I am also in full agreement with @EricTopol and others that it will be important to see more of the data to make further conclusions about this vaccine.
1/ Novavax UK first:
~90% protection again any symptomatic COVID-19. And that high level of protection was accomplished under conditions of very intense community transmission in the UK, which is a high bar. 1/n bit.ly/3oEpann
2/ (i.e., most likely a higher bar for protection than USA summer transmission, or anywhere with low level SARS2 transmission). And that was under conditions of high prevalence of the "UK variant" (B117), which is significantly more transmissible than the parental SARS2 strain.
3/ The Novavax vaccine was quite protective against both the parental strain and the UK variant, which is welcome news.
1/ Here's my review on adaptive immunity to COVID-19 and SARS-CoV-2. I hope you find it useful. It was a lot of work. Thanks to Prof Alex Sette @SetteLab and others for direct contributions and broader input over the year! cell.com/cell/fulltext/…@CellCellPress
2/ And thanks to all of the amazing scientists and labs around the world that have done so much work making incredible progress on these challenging COVID-19 immunology topics in the past year!
3/ FYI, here's the right version of Figure 1. It should be updated in the next version posted online.
2/ Definitely good news to see these data on the Pfizer vaccine working against the 501 variant. If anything, the vaccine works better against this variant. biorxiv.org/content/10.110…
3/ It isn't the end of the story, because the UK / SA variants have mutations in addition to 501, but these vaccine data are an important piece of the puzzle. As noted in the article, more is expected from labs in the coming weeks, but these results are expected & encouraging.
1/ One pre-print on B117 viral loads (i.e., B.1.1.7 SARS-CoV-2 ) found substantially higher viral loads (median 10-100 times). Another UK study found 3 times higher viral loads in people with B117 (Bonsall/Golubchik study). medrxiv.org/content/10.110…
2. The immune system can remember viruses. And there are multiple different parts of the immune system that can remember a virus in different ways, so the immune system can fight the virus in multiple ways.
3. Our data shows that the body’s immune system remembers novel coronavirus for at least 8 months after COVID-19, and multiple different branches of the immune system remember the virus.