Throughout much of history, claiming to be able to predict the future, particularly a future filled with death and disaster has been an effective way of becoming well known. Its perhaps worth considering some of the issues around Covid 19 to give this claim some context.
Among the 5 main variants there are a large number of sub variants and currently in the currently dominant Omicrom variant, more than 300 subvariants have been identified. Many of these have genetic changes that could alter the criteria that label them as “of concern”. The majority of these changes lead to alterations in the spike protein of the virus, particularly in the receptor binding domain. It seems that the number of changes in the spike protein correlates with the degree of antibody evasion seen in the virus. However, vaccination and prior infections do mean that all of the variants have to overcome the same antibody defences, this has lead to convergent evolution in which different strains share similar mutations in order to overcome these defences. It has been suggested that the greater the number of these changes, the faster the virus seems to take over from the previous dominant strains.
Really, predicting how the virus and the disease it causes will evolve, is really a triumph of hope over experience, we simply have to little information about the selective forces at work and what evidence we do have is inconsistent and confusing.
The initial indicators were that cases involving the variants BQ1 and BQ11 were increasingly being identified and they appeared to be set to become the dominant strains, however, the rates of these increases was highly variable depending on where the sampling was carried out. In some areas in which a rapid rise was detected, it suddenly seemed to stop, in the UK for example which appeared to be heading rapidly into a new wave of infections, the rate of increase has stalled with some suggestion that the numbers are actually dropping again. There are also, several other variants that appear to have greater immune evasion abilities and that have cause rapid increases then simply fizzled out. It is thought that the most immune evasive variant is in fact BA4.6, currently the second-most-prevalent strain in the U.S. And for many of the previous weeks, while its share of cases has increased over that time, (@ 11%), its growth nationally has been rather slow. Another new variant BF7 is also circulating in the US and is increasing, currently causing around 7% of cases. Its interesting that despite the evidence of antibody resistance, none of these variants stand out as particularly more dangerous, which is rather curious. So despite calls to increase surveillance, the reduced risks, seems to have reduced its importance, and the level of surveillance has actually fallen as concern shifts to other respiratory diseases and new information about older diseases. This means the data we have has become increasingly less reliable. We also need to consider that most of the variants identified for increased surveillance in the past and found in significant numbers of people, have simply disappeared from sight.Of course if a variant can resist the effects of circulating antibodies its hardly surprising that humoral antibodies will become increasingly less less effective in preventing initial infection and symptomatic disease. This will depend on the number of antibodies that are effected and their relative importance in resistance. Unfortunately most of the information we have only looks at overall antibody levels and we simply don't know the levels of antibodies needed to have a significant effect. Its certainly true that there are a significant number of cases arising in the vaccinated population and even in people during the periods they should have the highest levels. Measures of antibodies without some baseline level of known effectiveness really tells us nothing, a vaccine might be very good at creating an antibody response but that doesn't really tell us it effects on infection.Many virologists have suggested we should not consider a vaccine as offering significant protection from symptomatic infection, its function is in protecting people from serious disease and death, something which it appears to do quite well.Unfortunately for most viral diseases antibody levels provided a reliable measure of resistance, this actually meant that other parts of the immune system attracted far less attention and have been relatively poorly understood. Covid appears to have changed that, it seems that cell based immunity and tissue resident T cells play a very significant role in immunity and have their own persistent memory systems. Luckily all of the vaccines also stimulate significant T cell and tissue immunity, even though that was never really considered in their design. Currently there is no evidence that the effects of these systems can be effectively avoided by any of the variants
As most of these variants reduce the effectiveness of particular antibodies, it isn't surprising that they can impact on the effectiveness of antibody treatments used in prophylaxis for vulnerable people. This has caused significant concern.