Introduction: The coronavirus disease 2019 (COVID-19) pandemic led to the rapid development of vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), such as the Pfizer/BioNTech manufactured vaccine BNT162b2. In Japan, the preferential vaccination of healthcare workers began in January 2021 due to the high risk of exposure to SARS-CoV-2 in hospital settings, including at the Toho University Omori Medical Center. However, because BNT162b2 is based on a novel messenger ribonucleic acid (mRNA) vaccine platform, its ability to induce antigen-specific humoral and cellular immune responses has not yet been fully elucidated.
Methods: We examined the levels of antibodies and numbers of T cells in the blood, which were specific to the SARS-CoV-2 spike (S) protein, after BNT162b2 vaccination. The immune responses were evaluated among healthcare workers who had received two doses of BNT162b2.
Results: S protein-specific antibodies were induced in all participants following administration of two doses of BNT162b2. S protein-specific T cell expansion was also observed following vaccination. However, no correlation was observed between antibody titers and the magnitude of T cell responses among the participants.
Conclusions: Vaccine efficacy is often assessed using antigen-specific antibody titers, although T cells play an important role in adaptive immunity. Our findings indicate that the evaluation of antigen-specific T cell responses is necessary for accurately assessing the immunological effects of vaccination. Furthermore, these findings caution against reliance on antibody titers alone as a surrogate of vaccine-induced immunity.
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