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Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)-Specific Memory B Cells From Individuals With Diverse Disease Severities Recognize SARS-CoV-2 Variants of Concern.
Lyski, Zoe L; Brunton, Amanda E; Strnad, Matt I; Sullivan, Peter E; Siegel, Sarah A R; Tafesse, Fikadu G; Slifka, Mark K; Messer, William B.
  • Lyski ZL; Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, Oregon, USA.
  • Brunton AE; Oregon Health and Science University-Portland State University School of Public Health, Portland, Oregon, USA.
  • Strnad MI; Oregon Health and Science University-Portland State University School of Public Health, Portland, Oregon, USA.
  • Sullivan PE; Oregon Health and Science University-Portland State University School of Public Health, Portland, Oregon, USA.
  • Siegel SAR; Oregon Health and Science University-Portland State University School of Public Health, Portland, Oregon, USA.
  • Tafesse FG; Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, Oregon, USA.
  • Slifka MK; Division of Neuroscience, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, Oregon, USA.
  • Messer WB; Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, Oregon, USA.
J Infect Dis ; 225(6): 947-956, 2022 03 15.
Article in English | MEDLINE | ID: covidwho-1704045
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 / Memory B Cells Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: J Infect Dis Year: 2022 Document Type: Article Affiliation country: Infdis

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 / Memory B Cells Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: J Infect Dis Year: 2022 Document Type: Article Affiliation country: Infdis