Chat message
Slack / Private Message Drop, p.361 [SLACK_000575] · slack_pm:msg:03764
Page text: p.361 · original PDF
- Date
- 2021-01-05 16:13
- Type
- chat message · slack
- mentioned
- Kristian G. Andersen
- recipient
- Kristian G. Andersen, Edward C. Holmes, Andrew Rambaut
- speaker
- Robert F. Garry
- Topics
- Vaccines
Recipients on this medium are inferred from channel membership, not per-message addressing.
I know it's obvious but the problem comes when you start stacking up the mutations. 1.This is a pathogen that puts>20 glycans per monomer. There aren't going to be that many protective epitopes. So knock out 1, 2 or 3 and yeah the efficacy of any vaccine is going to take a hit. Knock efficacy below 50% and herd immunity is a long slowcrawl. 2. I also agree with @Kristian Andersen that looking at the Christmas card several of the mutations maybe are just kicking up fitness. The fact that the same site in a ZA variant was targeted for an insertion _in vitro_ [e.g. noimmune selection] D215G is bothersome. The FCS is already there.