Memory B-Cell Development After Asymptomatic or Mild Symptomatic SARS-CoV-2 Infection.

COVID-19 immunity SARS-CoV-2 adaptive immune response asymptomatic infection memory B cells mild infection

Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
28 12 2022
Historique:
received: 17 04 2022
accepted: 25 07 2022
pubmed: 28 7 2022
medline: 31 12 2022
entrez: 27 7 2022
Statut: ppublish

Résumé

The development of memory B cells after asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is not well understood. We compared spike antibody titers, pseudovirus neutralizing antibody titers, and memory B-cell responses among SARS-CoV-2 PCR-positive Marine recruits who either reported asymptomatic or symptomatic infection. Thirty-six asymptomatic participants exhibited similar spike IgG titers, spike IgA titers, and pseudovirus neutralization titers compared to 30 symptomatic participants. Pseudovirus neutralization and spike IgG titers showed significant positive correlations with frequency of memory B cells. Among young adults, asymptomatic SARS-CoV-2 infection induced antibody and memory B-cell responses comparable to mild symptomatic infection.

Sections du résumé

BACKGROUND
The development of memory B cells after asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is not well understood.
METHODS
We compared spike antibody titers, pseudovirus neutralizing antibody titers, and memory B-cell responses among SARS-CoV-2 PCR-positive Marine recruits who either reported asymptomatic or symptomatic infection.
RESULTS
Thirty-six asymptomatic participants exhibited similar spike IgG titers, spike IgA titers, and pseudovirus neutralization titers compared to 30 symptomatic participants. Pseudovirus neutralization and spike IgG titers showed significant positive correlations with frequency of memory B cells.
CONCLUSIONS
Among young adults, asymptomatic SARS-CoV-2 infection induced antibody and memory B-cell responses comparable to mild symptomatic infection.

Identifiants

pubmed: 35892131
pii: 6650397
doi: 10.1093/infdis/jiac319
pmc: PMC9384564
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Immunoglobulin G 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

18-22

Informations de copyright

Published by Oxford University Press on behalf of Infectious Diseases Society of America 2022.

Déclaration de conflit d'intérêts

Potential conflicts of interest. S. C. has consulted for GSK, JP Morgan, Citi, Morgan Stanley, Avalia NZ, Nutcracker Therapeutics, University of California, California State Universities, United Airlines, Adagio, and Roche. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Yu Kato (Y)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.

Nathaniel I Bloom (NI)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.

Peifang Sun (P)

Naval Medical Research Center, Silver Spring, Maryland, USA.

Corey A Balinsky (CA)

Henry Jackson Foundation, Bethesda, Maryland, USA.

Qi Qiu (Q)

Henry Jackson Foundation, Bethesda, Maryland, USA.

Ying Cheng (Y)

Leidos, Reston, Virginia, USA.

Vihasi Jani (V)

Henry Jackson Foundation, Bethesda, Maryland, USA.

Megan A Schilling (MA)

Naval Medical Research Center, Silver Spring, Maryland, USA.

Carl W Goforth (CW)

Naval Medical Research Center, Silver Spring, Maryland, USA.

Dawn L Weir (DL)

Naval Medical Research Center, Silver Spring, Maryland, USA.

Irene Ramos (I)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Stuart C Sealfon (SC)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Andrew G Letizia (AG)

Naval Medical Research Center, Silver Spring, Maryland, USA.

Shane Crotty (S)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.
Department of Medicine, Division of Infectious Diseases and Global Public Health, University of California San Diego, La Jolla, California, USA.

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Classifications MeSH