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Regulation of T Helper Cell Fate by TCR Signal Strength

T cells are critical in orchestrating protective immune responses to cancer and an array of pathogens. The interaction between a peptide MHC (pMHC) complex on antigen presenting cells (APCs) and T cell receptors (TCRs) on T cells initiates T cell activation, division, and clonal expansion in seconda...

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Detalles Bibliográficos
Autores principales: Bhattacharyya, Nayan D., Feng, Carl G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248325/
https://www.ncbi.nlm.nih.gov/pubmed/32508803
http://dx.doi.org/10.3389/fimmu.2020.00624
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author Bhattacharyya, Nayan D.
Feng, Carl G.
author_facet Bhattacharyya, Nayan D.
Feng, Carl G.
author_sort Bhattacharyya, Nayan D.
collection PubMed
description T cells are critical in orchestrating protective immune responses to cancer and an array of pathogens. The interaction between a peptide MHC (pMHC) complex on antigen presenting cells (APCs) and T cell receptors (TCRs) on T cells initiates T cell activation, division, and clonal expansion in secondary lymphoid organs. T cells must also integrate multiple T cell-intrinsic and extrinsic signals to acquire the effector functions essential for the defense against invading microbes. In the case of T helper cell differentiation, while innate cytokines have been demonstrated to shape effector CD4(+) T lymphocyte function, the contribution of TCR signaling strength to T helper cell differentiation is less understood. In this review, we summarize the signaling cascades regulated by the strength of TCR stimulation. Various mechanisms in which TCR signal strength controls T helper cell expansion and differentiation are also discussed.
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spelling pubmed-72483252020-06-05 Regulation of T Helper Cell Fate by TCR Signal Strength Bhattacharyya, Nayan D. Feng, Carl G. Front Immunol Immunology T cells are critical in orchestrating protective immune responses to cancer and an array of pathogens. The interaction between a peptide MHC (pMHC) complex on antigen presenting cells (APCs) and T cell receptors (TCRs) on T cells initiates T cell activation, division, and clonal expansion in secondary lymphoid organs. T cells must also integrate multiple T cell-intrinsic and extrinsic signals to acquire the effector functions essential for the defense against invading microbes. In the case of T helper cell differentiation, while innate cytokines have been demonstrated to shape effector CD4(+) T lymphocyte function, the contribution of TCR signaling strength to T helper cell differentiation is less understood. In this review, we summarize the signaling cascades regulated by the strength of TCR stimulation. Various mechanisms in which TCR signal strength controls T helper cell expansion and differentiation are also discussed. Frontiers Media S.A. 2020-05-19 /pmc/articles/PMC7248325/ /pubmed/32508803 http://dx.doi.org/10.3389/fimmu.2020.00624 Text en Copyright © 2020 Bhattacharyya and Feng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bhattacharyya, Nayan D.
Feng, Carl G.
Regulation of T Helper Cell Fate by TCR Signal Strength
title Regulation of T Helper Cell Fate by TCR Signal Strength
title_full Regulation of T Helper Cell Fate by TCR Signal Strength
title_fullStr Regulation of T Helper Cell Fate by TCR Signal Strength
title_full_unstemmed Regulation of T Helper Cell Fate by TCR Signal Strength
title_short Regulation of T Helper Cell Fate by TCR Signal Strength
title_sort regulation of t helper cell fate by tcr signal strength
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248325/
https://www.ncbi.nlm.nih.gov/pubmed/32508803
http://dx.doi.org/10.3389/fimmu.2020.00624
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