Cited by 21SARS-CoV-2 and COVID-19 ResearchImmune responses and vaccinationsVaccine Coverage and Hesitancy

Dynamics of antibody titers and cellular immunity among Japanese healthcare workers during the 6 months after receiving two doses of BNT162b2 mRNA vaccine

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Uwamino, Yoshifumi, Kurafuji, Toshinobu, Takato, Kumiko, Sakai, Akiko, Tanabe, Akiko, Noguchi, Masayo, Yatabe, Yoko, Arai, Tomoko +10 more·2022·Vaccine

Published version of a preprint

Abstract

Background The antibody titer is known to wane within months after receiving two doses of the Pfizer-BioNTech BNT162b2 mRNA SARS-CoV-2 vaccine. However, knowledge of the cellular immune response dynamics following vaccination is limited. This study to aimed to determine antibody and cellular immune responses following vaccination, and the incidence and determinants of breakthrough infection. Methods This prospective cohort study a 6-month follow-up period was conducted among Japanese healthcare workers. All participants received two doses of BNT162b2 vaccine. Anti-SARS-CoV-2 antibody titers and T-cell immune responses were measured in serum samples collected at several timepoints before and after vaccination. Results A total of 608 participants were included in the analysis. Antibody titers were elevated 3 weeks after vaccination and waned over the remainder of the study period. T-cell immune responses showed similar dynamics. Six participants without predisposing medical conditions seroconverted from negative to positive on the IgG assay for nucleocapsid proteins, indicating breakthrough SARS-CoV-2 infection. Five of the six breakthrough infections were asymptomatic. Conclusions Both humoral and cellular immunity waned within 6 months after BNT162b2 vaccination. The incidence of asymptomatic breakthrough infection within 6 months after vaccination was approximately one percent. Umin clinical trials registry id UMIN000043340.

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  1. [8]Uwamino Y, Wakui M, Yatabe Y, Nakagawa T, Sakai A, Kurafuji T, et al. Anti-SARS-CoV-2 cellular immunity in 571 vaccinees assessed using an interferon-γ release assay. medRxiv [Preprint]. https://doi.org/10.1101/2021.12.14.21267039. · DOI
  2. [20]Cele S. Jackson L. Khoury D.S. Khan K. Moyo-Gwete T. Tegally H. Omicron extensively but incompletely escapes Pfizer BNT162b2 neutralization Nature 602 7898 2022 654 656 10.1038/s41586-021-04387-1 35016196 PMC8866126 · DOI · Paper page

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Authors
Uwamino, Y., Kurafuji, T., Takato, K., Sakai, A., Tanabe, A., Noguchi, M., Yatabe, Y., Arai, T., Ohno, A., Tomita, Y., Shibata, A., Yokota, H., Yamasawa, W., Namkoong, H., Sato, Y., Hasegawa, N., Wakui, M., & Murata, M.
Affiliations
  • Keio University (JP)
  • Keio University Hospital (JP)
Corresponding author
Uwamino, Yoshifumi
Venue
Vaccine
Publisher
Elsevier BV
Published
2022-07
Volume
40
Issue
32
Pages
4538-4543
ISSN
0264-410X (ISSN-L)
OpenAlex
W4283072115
Cited by
21
References
18
Citations by year
2025: 5 · 2024: 4 · 2023: 9 · 2022: 3
FWCI
2.55
Type
journal article
Language
en
Open access
Locations
  • Vaccine (acceptedVersion)
  • medRxiv (acceptedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Japan Agency for Medical Research and Development (JP21fk0108469)
  • Public Foundation of Vaccination Research Center
  • School of Medicine, Keio University
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
  • Social Sciences › Health › Vaccine Coverage and Hesitancy
Keywords
BNT162b2 mRNA vaccine, SARS-CoV-2, antibody waning, T cell response, cell-mediated immunity, breakthrough infection, asymptomatic infection, healthcare workers, humoral immunity, Japanese population
MeSH terms
COVID-19, SARS-CoV-2, COVID-19 Vaccines, mRNA Vaccines, BNT162 Vaccine, Antibodies, Viral, Health Personnel, Humans, Immunity, Cellular, Japan, Prospective Studies, Vaccines, Synthetic

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