| Literature DB >> 34865053 |
Zoe L Lyski1, Amanda E Brunton2, Matt I Strnad2, Peter E Sullivan2, Sarah A R Siegel2, Fikadu G Tafesse1, Mark K Slifka3, William B Messer1,2,4.
Abstract
The unprecedented severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has called for substantial investigations into the capacity of the human immune system to protect against reinfection and keep pace with the evolution of SARS-CoV-2. We evaluated the magnitude and durability of the SARS-CoV-2-specific antibody responses against parental WA-1 SARS-CoV-2 receptor-binding domain (RBD) and a representative variant of concern (VoC) RBD using antibodies from 2 antibody compartments: long-lived plasma cell-derived plasma antibodies and antibodies encoded by SARS-CoV-2-specific memory B cells (MBCs). Thirty-five participants naturally infected with SARS-CoV-2 were evaluated; although only 25 of 35 participants had VoC RBD-reactive plasma antibodies, 34 of 35 (97%) participants had VoC RBD-reactive MBC-derived antibodies. Our finding that 97% of previously infected individuals have MBCs specific for variant RBDs provides reason for optimism regarding the capacity of vaccination, prior infection, and/or both, to elicit immunity with the capacity to limit disease severity and transmission of VoCs as they arise and circulate.Entities:
Keywords: COVID-19; antibody; disease severity; limiting dilution assay; memory B-cell; variant of concern
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Year: 2022 PMID: 34865053 PMCID: PMC8922005 DOI: 10.1093/infdis/jiab585
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226