You may recall on August 6 the SA trial announced 71% effectiveness against Delta hospitalization, but didn't say anything about effectiveness against disease, which is the default metric and the one used if you are gonig to report only one number.
Some surmised that effectiveness against Delta disease must be very unimpressive, or else it would have been reported alongside the hospitalization numbers on 8/6 (which were already unimpressive).
This has been proven correct.
That the SA trial is only willing to issue positive statements is understandable because they received the J&J vaccine free to provide to their HCWs. Not good to bite the hand that feeds, and better to avoid complaints re the choice of vaccine.
All understandable, but we (and the press) just need to factor this into the interpretation of their statements.
Instead the press has been dutifully repeating the one-sided statements from the SA trial, e.g. below
Indeed anything less than 90% is being considered unacceptable to RNA recipients. Indeed FDA head Janet Woodcock recently stated the goal of boosters for Pfizer and Moderna vaccinees is to prevent any drop in effectiveness against hospitalization. webmd.com/coronavirus-in…
Yet J&J produces only 71% protection against hospitalization (vs >90% for RNA vaccines) and ~50% protection against disease (vs ~80% for RNA vaccines at this point in time in the US). Quite clearly it is J&J vaccinees who need the boost first, not RNA vaccinees.
@PaulSaxMD and I supported J&J recipients getting boosters at the same schedule as RNA vaccines. We pointed out J&J efficacy vs Delta was unknown at the time of writing, but the South Africa hospitalizations and breakthrough indicators suggested it's worse nytimes.com/2021/08/29/opi…
Based on DC numbers, I had estimated J&J effectiveness of 50%.
So today's unofficial announcement from South Africa matches real-world data from the US as well.
It is now clear that J&J has worse efficacy on Delta vs 2 doses of RNA vaccines, at the same time post vaccine, for both infection (50 vs >80%) and hospitalizations (71 vs >90%).
I hope the issue can get officially acknowledged soon.
Colorado figures match DC and South Africa.
Relative protection against disease roughly 80/70/50% Moderna/Pfizer/J&J
"“I think we should have some humility in that nobody really knows” if a combination approach helps, she said."
We know from Stephensen and Barouch study, and the 90,000 people who did a RNA boost after J&J can be studied. More info at our op-ed at nytimes.com/2021/08/29/opi…
"“If one had shown more risk than the other, they would have said so,” she said."
One has – see above. And they haven't said so.
Even without the evidence above, we've learned that that CDC prefers not to say some things. So not sure anyone should find CDC silence reassuring.
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2) The editorial takes the form of a metaanalysis of vaccine efficacy, but it's the worst statistical malpractice I've ever seen. Fortunately it's short (one figure of 4 panels), so hopefully we can get through it quickly and point out the major issues.
Panel A: What is this??? Studies are grouped by efficacy ranges of 50-80, 80-90, and 90-100 for disease, then their average efficacy for all disease and severe disease are plotted. Why??? I'll try to be polite but I'm upset by this. It's an insult to human intelligence.
And before anyone complains the CIs are overlapping, that's a sophomoric complaint. Remember that's the 95% CI, and 95% is an arbitrary bar. Also there are other data that show J&J's lower effectiveness on hospitalization, such as below (pre-Delta)
🧵We discussed how mucosal antibodies function to block SARSCoV2 infection. A study on this just posted from my Stanford colleague Michal Tal and UToronto collaborator Jennifer Gommerman.
Interesting: RNA and J&J make Abs in saliva, but neutralizing levels only detected with RNA
2) First, as a reminder, the role of mucosal antibodies (thought mostly to be IgA, but we'll revisit that in a moment) is to block viruses, once they land on your mucous membranes, from entering your cells.
1) There was an ACIP meeting today, but nothing newsworthy happened. CDC briefing materials (as posted at cdc.gov/vaccines/acip/…) are limiting the ability of ACIP to independently and intelligently assess data.
2) Most concerning, CDC continues to withhold J&J data by omitting it entirely or lumping it together with the 10x larger Pfizer+Moderna data so it becomes a rounding error. No wonder ACIP is not able to make any recommendations specifically for J&J cdc.gov/vaccines/acip/…
3) But the data exist, and is becoming increasingly in plain sight, showing higher case and hospitalization rates for J&J than for Pfizer and Moderna in the real world against Delta
In a recent thread I posited that mechanisms of antibody production, viral resistance, and somatic hypermutation can explain why pre-Delta vaccines block most Delta infections but not peak virus levels once infected, yet still limit late disease.
Most neutralization of SARSCoV2 infection is performed by antibodies against the spike (S) protein, and the vaccines used in the US include only S and no other parts of SARSCoV2, so we'll concentrate on S as the antigen, i.e. the protein targeted by antibodies or T cell receptors
Your body has millions to billions of resting/naive B cells, each with an unique surface-bound antibody or immunoglobulin (Ig), just waiting to find their match to foreign particles. You also have T cells with unique T cell receptors (TCRs) ncbi.nlm.nih.gov/pmc/articles/P…
In our @nytimes opinion piece, Dr. Paul Sax (Brigham and Women's Hospital) and I present why the data support RNA boosters for immunocompromised J&J patients, now possible off-label.
And when boosters kick in for everyone, we hope #JnJers are given good options at the same time.
And that's why we think the data we have sitting in databases on J&J VE need to be openly discussed, and why boosters for #JnJers are needed at least at the same time as boosters for everyone else.