Transcriptional and Metabolic Control of Memory B Cells and Plasma Cells.


Journal

Annual review of immunology
ISSN: 1545-3278
Titre abrégé: Annu Rev Immunol
Pays: United States
ID NLM: 8309206

Informations de publication

Date de publication:
26 04 2021
Historique:
pubmed: 9 2 2021
medline: 18 5 2021
entrez: 8 2 2021
Statut: ppublish

Résumé

For many infections and almost all vaccines, neutralizing-antibody-mediated immunity is the primary basis and best functional correlate of immunological protection. Durable long-term humoral immunity is mediated by antibodies secreted by plasma cells that preexist subsequent exposures and by memory B cells that rapidly respond to infections once they have occurred. In the midst of the current pandemic of coronavirus disease 2019, it is important to define our current understanding of the unique roles of memory B cells and plasma cells in immunity and the factors that control the formation and persistence of these cell types. This fundamental knowledge is the basis to interpret findings from natural infections and vaccines. Here, we review transcriptional and metabolic programs that promote and support B cell fates and functions, suggesting points at which these pathways do and do not intersect.

Identifiants

pubmed: 33556247
doi: 10.1146/annurev-immunol-093019-125603
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

345-368

Auteurs

Tyler J Ripperger (TJ)

Department of Immunobiology, University of Arizona College of Medicine-Tucson, Tucson, Arizona 85724, USA; email: ripperger@arizona.edu, deeptab@arizona.edu.

Deepta Bhattacharya (D)

Department of Immunobiology, University of Arizona College of Medicine-Tucson, Tucson, Arizona 85724, USA; email: ripperger@arizona.edu, deeptab@arizona.edu.

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Classifications MeSH