Abstract
Waning antibody levels against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and the emergence of variants of concern (VOC) highlight the need for booster vaccinations. This is particularly important for the elderly population, who are at a higher risk of developing severe Coronavirus disease 2019 (COVID-19) disease. Whilst studies have shown increased antibody responses following booster vaccination, understanding the changes in T and B cell compartments induced by a third vaccine dose remains limited.
We analysed the humoral and cellular responses in subjects who received either a homologous mRNA booster vaccine (BNT162b2+BNT162b2+BNT162b2; 'BBB') or a heterologous mRNA booster vaccine (BNT162b2+BNT162b2+mRNA-1273; 'BBM') at day 0 (pre-booster), day 7 and day 28 (post-booster).
Compared to BBB, elderly individuals (≥60 years old) who received the BBM vaccination regimen display higher levels of neutralising antibodies a gainst the Wuhan and Delta strains along with a higher boost in IgG memory B cells, particularly against the Omicron variant. Circulating Th1, Th2, Th17 and Tfh responses were also increased in elderly individuals given the BBM regimen. While mRNA vaccines increase antibody, T cell and B cell responses against SARS-CoV-2 one month after receiving the third dose booster, the efficacy of the booster vaccine strategies may vary depending on age group and regimen combination.
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