Cited by 338T-cell and B-cell ImmunologyPsoriasis: Treatment and PathogenesisImmunotherapy and Immune Responses

CD4+ T cell memory

Open access
Künzli, Marco, Masopust, David·2023·Nature Immunology

Abstract

Specialized subpopulations of CD4+ T cells survey major histocompatibility complex class II-peptide complexes to control phagosomal infections, help B cells, regulate tissue homeostasis and repair or perform immune regulation. Memory CD4+ T cells are positioned throughout the body and not only protect the tissues from reinfection and cancer, but also participate in allergy, autoimmunity, graft rejection and chronic inflammation. Here we provide updates on our understanding of the longevity, functional heterogeneity, differentiation, plasticity, migration and human immunodeficiency virus reservoirs as well as key technological advances that are facilitating the characterization of memory CD4+ T cell biology.

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References 180 · Cited by 338

Authors
Künzli, M., & Masopust, D.
Affiliations
University of Minnesota (US)
Corresponding author
Masopust, David
Venue
Nature Immunology
Published
2023-05-08
Volume
24
Issue
6
Pages
903-914
ISSN
  • 1529-2908 (ISSN-L)
  • 1529-2916
OpenAlex
W4375859102
Cited by
338
References
180
Citations by year
2026: 91 · 2025: 131 · 2024: 100 · 2023: 16
FWCI
9.45
Type
journal article
Language
en
Open access
Locations
  • Nature Immunology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Foundation for the National Institutes of Health (R01CA238439, R01AI146032, R01AI084913, R01AI150600)
  • Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (P2B-SP3-200187)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
Keywords
memory CD4+ T cells, T cell differentiation, T cell plasticity, T cell migration, HIV reservoir, T cell longevity, functional heterogeneity, peptide-MHC class II complexes, B cell help, tissue homeostasis, immune regulation, allergy, autoimmunity, graft rejection, chronic inflammation
MeSH terms
Memory T Cells, Humans, Immunologic Memory, CD4-Positive T-Lymphocytes

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