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DOI 10.3389/fimmu.2024.1445653

Медицинская библиотека · Frontiers in immunology · 2024

Robust and persistent B-cell responses following SARS-CoV-2 vaccine determine protection from SARS-CoV-2 infection.

Byrne Joanne, Gu Lili, Garcia-Leon Alejandro, Gaillard Colette Marie, Saini Gurvin, Alalwan Dana, Tomás-Cortázar Julen, Kenny Grace, Donohue Sean, Reynolds Bearach, O'Gorman Tessa, Landay Alan, Doran Peter, Stemler Jannik, Koehler Philipp, Cox Rebecca Jane, Olesen Ole F, Lelievre Jean-Daniel, O'Broin Cathal, Savinelli Stefano, Feeney Eoin R, O'Halloran Jane A, Cotter Aoife, Horgan Mary, Kelly Christine, Sadlier Corrina, de Barra Eoghan, Cornely Oliver A, Gautier Virginie, Mallon Patrick Wg

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Аннотация

INTRODUCTION

A clear immune correlate of protection from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has not been defined. We explored antibody, B-cell, and T-cell responses to the third-dose vaccine and relationship to incident SARS-CoV-2 infection.

METHODS

Adults in a prospective cohort provided blood samples at day 0, day 14, and 10 months after the third-dose SARS-CoV-2 vaccine. Participants self-reported incident SARS-CoV-2 infection. Plasma anti-SARS-CoV-2 receptor-binding domain (RBD) and spike-subunit-1 and spike-subunit-2 antibodies were measured. A sub-study assessed SARS-CoV-2-specific plasma and memory B-cell and memory T-cell responses in peripheral blood mononuclear cells by enzyme-linked immunospot. Comparative analysis between participants who developed incident infection and uninfected participants utilised non-parametric t-tests, Kaplan-Meier survival analysis, and Cox proportional hazard ratios.

RESULTS

Of the 132 participants, 47 (36%) reported incident SARS-CoV-2 infection at a median 16.5 (16.25-21) weeks after the third-dose vaccination. RBD titres and B-cell responses, but not T-cell responses, increased after the third-dose vaccine. Whereas no significant difference in day 14 antibody titres or T-cell responses was observed between participants with and without incident SARS-CoV-2 infection, RBD memory B-cell frequencies were significantly higher in those who did not develop infection [10.0% (4.5%-16.0%) versus 4.9% (1.6%-9.3%), p = 0.01]. RBD titres and memory B-cell frequencies remained significantly higher at 10 months than day 0 levels (p < 0.01).

DISCUSSION: Robust antibody and B-cell responses persisted at 10 months following the third-dose vaccination. Higher memory B-cell frequencies, rather than antibody titres or T-cell responses, predicted protection from subsequent infection, identifying memory B cells as a correlate of protection.

Для цитирования: Byrne Joanne, Gu Lili, Garcia-Leon Alejandro, Gaillard Colette Marie, Saini Gurvin, Alalwan Dana, Tomás-Cortázar Julen, Kenny Grace, Donohue Sean, Reynolds Bearach, O'Gorman Tessa, Landay Alan, Doran Peter, Stemler Jannik, Koehler Philipp, Cox Rebecca Jane, Olesen Ole F, Lelievre Jean-Daniel, O'Broin Cathal, Savinelli Stefano, Feeney Eoin R, O'Halloran Jane A, Cotter Aoife, Horgan Mary, Kelly Christine, Sadlier Corrina, de Barra Eoghan, Cornely Oliver A, Gautier Virginie, Mallon Patrick Wg. Robust and persistent B-cell responses following SARS-CoV-2 vaccine determine protection from SARS-CoV-2 infection.. Frontiers in immunology. 2024. DOI: 10.3389/fimmu.2024.1445653.

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