Long-lasting antibody B-cell responses to SARS-CoV-2 three years after the onset of the pandemic

Immune memory is essential for the effectiveness of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination. In the current context of the pandemic, with a diminished vaccine efficacy against emerging variants, it remains crucial to perform long-term studies to evaluate the durability and quality of immune responses. Here, we examined the antibody and memory B-cell responses in a cohort of 113 healthcare workers with distinct exposure histories over a 3-year period. Previously infected and naive participants developed comparable humoral responses by 17 months after receiving a full three-dose mRNA vaccination. In addition, both maintained a substantial SARS-CoV-2-reactive memory B-cell pool, associated with a lower incidence of breakthrough infections in naive participants. Of note, previously infected participants developed an expanded SARS-CoV-2-reactive CD27<sup>-</sup>CD21<sup>-</sup> atypical B-cell population that remained stable throughout the follow-up period. Thus, previous SARS-CoV-2 infection differentially imprints the memory B-cell compartment without compromising the development of long-lasting humoral responses.

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Publication Details

Journal
Cell Reports
Published
2025-04-01
DOI
https://doi.org/10.1016/j.celrep.2025.115498
Citations
4
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
5.58
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article

Long-lasting antibody B-cell responses to SARS-CoV-2 three years after the onset of the pandemic

Marta Vidal, Ester Aparicio, Benjamin Trinité, Anna Ramírez‐Morros et al.
4 citations
Cell Reports
SARS-CoV-2 and COVID-19 Research
5.58
article

Long-lasting antibody B-cell responses to SARS-CoV-2 three years after the onset of the pandemic

Marta Vidal, Ester Aparicio, Benjamin Trinité, Anna Ramírez‐Morros, Josep Vidal‐Alaball, Pere Santamaría, Alfons Jiménez, Sílvia Marfil, Gemma Moncunill, Luís Izquierdo, Ruth Aguilar, Diana Barrios, Edwards Pradenas, Luis M. Molinos‐Albert, Pau Serra, Rocío Rubio, Anna Ruiz‐Comellas, Julià Blanco, Carlota Dobaño, Mar Canyelles, Cèlia Torres, Carla Martín-Pérez
article en
4 citations

Abstract

Immune memory is essential for the effectiveness of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination. In the current context of the pandemic, with a diminished vaccine efficacy against emerging variants, it remains crucial to perform long-term studies to evaluate the durability and quality of immune responses. Here, we examined the antibody and memory B-cell responses in a cohort of 113 healthcare workers with distinct exposure histories over a 3-year period. Previously infected and naive participants developed comparable humoral responses by 17 months after receiving a full three-dose mRNA vaccination. In addition, both maintained a substantial SARS-CoV-2-reactive memory B-cell pool, associated with a lower incidence of breakthrough infections in naive participants. Of note, previously infected participants developed an expanded SARS-CoV-2-reactive CD27<sup>-</sup>CD21<sup>-</sup> atypical B-cell population that remained stable throughout the follow-up period. Thus, previous SARS-CoV-2 infection differentially imprints the memory B-cell compartment without compromising the development of long-lasting humoral responses.

Cell ReportsVol. 44(4)
Barcelona Institute for Global Health (ES), Consorci Institut D'Investigacions Biomediques August Pi I Sunyer (ES)
Good health and well-being
Openalex Percentile: Top 4%
SARS-CoV-2 and COVID-19 Research
5.58
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