Abstract
The responsiveness/cross-binding of vaccine-induced memory B cells/MBCs to previous and emerging divergent SARS-CoV-2 variants (e.g., Omicron) is understudied. In this longitudinal study subjects receiving two or three doses of monovalent ancestral strain-containing COVID-19 mRNA vaccine were evaluated. In contrast to others, we observed significantly lower frequencies of MBCs reactive to the receptor-binding domain/RBD, the N-terminal domain/NTD, and the S1 of Omicron/BA.1, compared to Wuhan and Delta, even after a 3rd vaccine dose/booster. Our study is a proof of concept that MBC cross-reactivity to variants with greater sequence divergence from the vaccine strain may be overestimated and suggests that these variants may exhibit immune escape with reduced recognition by circulating pre-existing MBCs upon infection.
Original language | English (US) |
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Pages (from-to) | 912-917 |
Number of pages | 6 |
Journal | Vaccine |
Volume | 42 |
Issue number | 4 |
DOIs | |
State | Published - Feb 6 2024 |
Keywords
- Antibodies, neutralizing
- B cells
- COVID-19
- Humoral immune responses
- Immunological memory
- SARS-CoV-2
- Vaccine
- Variants of concern
ASJC Scopus subject areas
- Molecular Medicine
- General Immunology and Microbiology
- General Veterinary
- Public Health, Environmental and Occupational Health
- Infectious Diseases