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I'm sure it's not the concern of "most scientists", which is why I said virologists.
most virologists then
SARS-CoV-2 has so far only explored a fraction of its mutagenic space, and that, in the wild, in a relatively short time. Besides RBD mutations, the spike has an unusually high degree of conformational plasticity and that even contributes to antibody evasion through concealment of key epitopes in the NTD, where the virus has been playing with a lot of deletions. Now we are seeing co-infections, sooner or later we are probably also going to start seeing recombination events as well.
There's plenty about the spike protein that is highly conserved across species, and it's plasticity is as expected given it's mechanism as a fusion protein. The idea that it's going to suddenly start evading the current vaccines such that these vaccines cease to be effective at preventing serious disease and death is a big stretch.
Absolutely, but that unfortunately cuts both ways (eg vaccine sera variant efficacy studies).
Here it still applies, as vaccine sera studies don't tell us about the T-cell response which is likely to be polyclonal to a variety of spike protein epitopes outside the RBD and thus not comprised by the mutations under discussion.
I think the fact that both the media and many virologists unused to the public understanding of science have in their public pronouncements focused on standard vaccine effectiveness as measured in phase III trials using "disease", rather than "severe disease and death" has lead to fear and vaccine hesitancy in some quarters which could prove highly damaging.
There's no indication whatsoever that current vaccines will not have a considerably beneficial affect against the so-called South Africa strain.
Sure we need to update vaccines as time goes on, but the idea we should withhold current vaccines for lack of efficacy against current variants, or that we shouldn't extend the gap between doses due to concern about mutations are mistakes that are 100% likely to result in many deaths.