Impact of the bivalent COVID-19 booster on spike-specific t cell responses

The emergence of SARS-CoV-2 variants during the COVID-19 pandemic prompted updates to the original vaccines to improve immunogenicity against novel SARS-CoV-2 variants. Since 2022, vaccination guidelines introduced updated mRNA boosters, starting with a bivalent formulation that included the original and Omicron BA.4/BA.5 spike sequences, which emerged in late 2021. In this study, we characterized the spike-specific T cell response following the bivalent booster vaccination in humans. We performed an in-depth profiling of T cells, assessing activation markers, cytokine production and the impact of previous COVID-19 infection in the response to different spike variants. Overall, our results are consistent with the bivalent booster having a limited influence on spike-T cell responses, with similar magnitude and functionality observed toward the Omicron BA.4/BA.5 variant and the ancestral spike. Nonetheless, the booster proved to be beneficial for immunocompetent individuals with poor or declining T cell responses, increasing the frequency of specific T cells in blood.

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Publication Details

Journal
Vaccine
Published
2025-11-20
DOI
https://doi.org/10.1016/j.vaccine.2025.127995
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
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article

Impact of the bivalent COVID-19 booster on spike-specific t cell responses

Alessandro Sette, Rosa Isela Gálvez, Daniela Weiskopf, Amparo Martínez-Pérez et al.
Vaccine
SARS-CoV-2 and COVID-19 Research
article

Impact of the bivalent COVID-19 booster on spike-specific t cell responses

Alessandro Sette, Rosa Isela Gálvez, Daniela Weiskopf, Amparo Martínez-Pérez, Alba Grifoni, Peter K. Gregersen
article en

Abstract

The emergence of SARS-CoV-2 variants during the COVID-19 pandemic prompted updates to the original vaccines to improve immunogenicity against novel SARS-CoV-2 variants. Since 2022, vaccination guidelines introduced updated mRNA boosters, starting with a bivalent formulation that included the original and Omicron BA.4/BA.5 spike sequences, which emerged in late 2021. In this study, we characterized the spike-specific T cell response following the bivalent booster vaccination in humans. We performed an in-depth profiling of T cells, assessing activation markers, cytokine production and the impact of previous COVID-19 infection in the response to different spike variants. Overall, our results are consistent with the bivalent booster having a limited influence on spike-T cell responses, with similar magnitude and functionality observed toward the Omicron BA.4/BA.5 variant and the ancestral spike. Nonetheless, the booster proved to be beneficial for immunocompetent individuals with poor or declining T cell responses, increasing the frequency of specific T cells in blood.

VaccineVol. 69
Northwell Health (US), La Jolla Institute for Immunology (US), Feinstein Institute for Medical Research (US)
Openalex Percentile: Top 59%
SARS-CoV-2 and COVID-19 Research
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