Toward a general model of CD4+ T cell subset specification and memory cell formation
- PMID: 36921574
- PMCID: PMC10084496
- DOI: 10.1016/j.immuni.2023.02.010
Toward a general model of CD4+ T cell subset specification and memory cell formation
Abstract
In the past few decades, a number of transformative discoveries have been made regarding memory CD8+ T cell biology; meanwhile, the CD4+ T cell field has lagged behind this progress. This perspective focuses on CD4+ helper T (Th) cell subset specification and memory cell formation. Here, we argue that the sheer number of Th effector and memory cell subsets and a focus on their differences have been a barrier to a general model of CD4+ memory T cell formation that applies to all immune responses. We highlight a bifurcation model that relies on an IL-2 signal-dependent switch as an explanation for the balanced production of diverse Th memory cells that participate in cell-mediated or humoral immunity in most contexts.
Copyright © 2023 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests The authors declare no competing interests.
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References
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- Rudolph MG, Stanfield RL, and Wilson IA (2006). How TCRs bind MHCs, peptides, and coreceptors. Annu. Rev. Immunol 24, 419–466. - PubMed
-
- Jenkins MK, Khoruts A, Ingulli E, Mueller DL, McSorley SJ, Reinhardt RL, Itano A, and Pape KA (2001). In vivo activation of antigen-specific CD4 T cells. Annu. Rev. Immunol 19, 23–45. - PubMed
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