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there is a firestorm of protest against the highly controversial and in my view erroneous decision, to delay second vaccine shots for high risk groups for 16 weeks. this applies to those over 80, and immune compromised individuals who have been denied a second coronavirus vaccine shot within the timeline suggested by the vaccine manufacturer. such timelines between shots was based on trial data for mrna vaccines submitted for regulatory approval. this is the type of novel vaccine that almost all such high risk people were given, since these vaccines were shown to have the highest efficacy in preventing infection.
the delay to 16 weeks for the second shot was the result of a lack of vaccine availability. it was based on the unproven hope that such delay could safely allow for early vaccination of more people with a protective, albeit diminished effectiveness of a single dose.
the national advisory committee on immunization (naci) suggested that such deferral of a second dose was likely safe, based on no real data. it was an extrapolation from data not from mrna vaccines, but from viral vector vaccines, which were less effective in preventing infection, but highly effective in preventing death.
while this position could be understood, if not agreed with, when there was no data, it is untenable now that there is a growing body of data against it.
trial data of the new vaccines did not adequately represent these ultra high risk groups for vaccine efficacy. real world data showed a great reduction in nursing home and other deaths with vaccination and to some degree after the first dose. much of this data came before the more contagious and dangerous b 1.1.7 strain, first detected in the united kingdom, greatly dominated infections in many countries.
studies from germany and england, and now b.c. have shown highly concerning lack of antibody production after a first dose in many elderly, immune compromised and cancer patients which can be greatly boosted by a timely second dose. in the uk study of cancer patients, 95 per cent developed adequate antibody response with two appropriately timed pfizer doses but only 43 per cent if the second dose was delayed.