Evolution of long-term vaccine-induced and hybrid immunity in healthcare workers after different COVID-19 vaccine regimens.

Abstract

Both infection and vaccination, alone or in combination, generate antibody and Tcell responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, the maintenance of such responses-and hence protection from disease-requires careful characterization. In a large prospective study of UK healthcare workers (HCWs) (Protective Immunity from T Cells in Healthcare Workers [PITCH], within the larger SARS-CoV-2 Immunity and Reinfection Evaluation [SIREN] study), we previously observed that prior infection strongly affected subsequent cellular and humoral immunity induced after long and short dosing intervals of BNT162b2 (Pfizer/BioNTech) vaccination. Here, we report longer follow-up of 684 HCWs in this cohort over 6-9months following two doses of BNT162b2 or AZD1222 (Oxford/AstraZeneca) vaccination and up to 6months following a subsequent mRNA booster vaccination. We make three observations: first, the dynamics of humoral and cellular responses differ; binding and neutralizing antibodies declined, whereas T and memory B cell responses were maintained after the second vaccine dose. Second, vaccine boosting restored immunoglobulin (Ig) G levels; broadened neutralizing activity against variants of concern, including Omicron BA.1, BA.2, and BA.5; and boosted Tcell responses above the 6-month level after dose 2. Third, prior infection maintained its impact driving larger and broader Tcell responses compared with never-infected people, a feature maintained until 6months after the third dose. Broadly cross-reactive Tcell responses are well maintained over time-especially in those with combined vaccine and infection-induced immunity ("hybrid" immunity)-and may contribute to continued protection against severe disease. Department for Health and Social Care, Medical Research Council.