Bivalent mRNA booster vaccination recalls cellular and antibody immunity against antigenically divergent SARS-CoV-2 spike antigens

The ongoing rollout of SARS-CoV-2 vaccines lags behind rapid viral evolution. Updated vaccine immunogens elicit neutralising antibodies against the component strain. However, protection against future SARS-CoV-2 variants is unclear. Here, we sought to understand factors underpinning serological breadth following bivalent BA.1 vaccination. Booster vaccination of 33 individuals elicited robust and durable antibody responses against component vaccine antigens and elevated frequencies of spike-specific CD4 and CD8 T cells. Immunisation predominantly drove recall of cross-reactive memory B cells which also recognised XBB.1.5 spike, with significantly enhanced neutralisation titres against XBB virus seen within 91% of participants. Multivariate regression indicated that both baseline neutralising titres and spike-specific CD4 T cell frequencies were strong predictors of ancestral, BA.1 and XBB neutralisation post-immunisation. These data highlight that updated SARS-CoV-2 vaccines recall cross-reactive memory that maintains recognition of antigenically evolved viral variants and suggests T cell help and prior antibody titres underpin robust vaccine-induced neutralising activity.

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Publication Details

Journal
npj Vaccines
Published
2025-04-18
DOI
https://doi.org/10.1038/s41541-025-01129-6
Citations
5
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
6.98

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article

Bivalent mRNA booster vaccination recalls cellular and antibody immunity against antigenically divergent SARS-CoV-2 spike antigens

Mai-Chi Trieu, Adam K. Wheatley, Robyn Esterbauer, Miles P. Davenport et al.
5 citations
npj Vaccines
SARS-CoV-2 and COVID-19 Research
6.98
article

Bivalent mRNA booster vaccination recalls cellular and antibody immunity against antigenically divergent SARS-CoV-2 spike antigens

Mai-Chi Trieu, Adam K. Wheatley, Robyn Esterbauer, Miles P. Davenport, Arnold Reynaldi, David S. Khoury, Joseph Sasadeusz, Jennifer A. Juno, Stephen John Kent, Jennifer Audsley, Hyon‐Xhi Tan, Wen Shi Lee, Rebecca Jane Cox, Deborah Cromer, Andrew P. Kelly
article en
5 citations

Abstract

The ongoing rollout of SARS-CoV-2 vaccines lags behind rapid viral evolution. Updated vaccine immunogens elicit neutralising antibodies against the component strain. However, protection against future SARS-CoV-2 variants is unclear. Here, we sought to understand factors underpinning serological breadth following bivalent BA.1 vaccination. Booster vaccination of 33 individuals elicited robust and durable antibody responses against component vaccine antigens and elevated frequencies of spike-specific CD4 and CD8 T cells. Immunisation predominantly drove recall of cross-reactive memory B cells which also recognised XBB.1.5 spike, with significantly enhanced neutralisation titres against XBB virus seen within 91% of participants. Multivariate regression indicated that both baseline neutralising titres and spike-specific CD4 T cell frequencies were strong predictors of ancestral, BA.1 and XBB neutralisation post-immunisation. These data highlight that updated SARS-CoV-2 vaccines recall cross-reactive memory that maintains recognition of antigenically evolved viral variants and suggests T cell help and prior antibody titres underpin robust vaccine-induced neutralising activity.

npj VaccinesVol. 10(1)
The Royal Melbourne Hospital (AU), The University of Melbourne (AU), Haukeland University Hospital (NO), UNSW Sydney (AU), Peter Doherty Institute (AU), University of Bergen (NO)
Sylvia and Charles Viertel Charitable Foundation, Universitetet i Bergen, Haukeland Universitetssjukehus, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 3%
SARS-CoV-2 and COVID-19 Research
6.98
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