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Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells

During chronic antigen exposure, a subset of exhausted CD8(+) T cells differentiate into stem cell-like or progenitor-like T cells expressing both transcription factor Tcf-1 (T cell factor-1) and co-inhibitory receptor PD-1. These Tcf-1(+) stem-like or progenitor exhausted T cells represent the key...

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Autores principales: Ma, Chaoyu, Zhang, Nu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9767944/
https://www.ncbi.nlm.nih.gov/pubmed/36569850
http://dx.doi.org/10.3389/fimmu.2022.1074698
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author Ma, Chaoyu
Zhang, Nu
author_facet Ma, Chaoyu
Zhang, Nu
author_sort Ma, Chaoyu
collection PubMed
description During chronic antigen exposure, a subset of exhausted CD8(+) T cells differentiate into stem cell-like or progenitor-like T cells expressing both transcription factor Tcf-1 (T cell factor-1) and co-inhibitory receptor PD-1. These Tcf-1(+) stem-like or progenitor exhausted T cells represent the key target for immunotherapies. Deeper understanding of the biology of Tcf-1(+)PD-1(+) CD8(+) T cells will lead to rational design of future immunotherapies. Here, we summarize recent findings about the migratory and resident behavior of Tcf-1(+) T cells. Specifically, we will focus on TGF-β-dependent lymphoid tissue residency program of Tcf-1(+) T cells, which may represent a key to understanding the differentiation and maintenance of Tcf-1(+) stem-like CD8(+) T cells during persistent antigen stimulation.
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spelling pubmed-97679442022-12-22 Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells Ma, Chaoyu Zhang, Nu Front Immunol Immunology During chronic antigen exposure, a subset of exhausted CD8(+) T cells differentiate into stem cell-like or progenitor-like T cells expressing both transcription factor Tcf-1 (T cell factor-1) and co-inhibitory receptor PD-1. These Tcf-1(+) stem-like or progenitor exhausted T cells represent the key target for immunotherapies. Deeper understanding of the biology of Tcf-1(+)PD-1(+) CD8(+) T cells will lead to rational design of future immunotherapies. Here, we summarize recent findings about the migratory and resident behavior of Tcf-1(+) T cells. Specifically, we will focus on TGF-β-dependent lymphoid tissue residency program of Tcf-1(+) T cells, which may represent a key to understanding the differentiation and maintenance of Tcf-1(+) stem-like CD8(+) T cells during persistent antigen stimulation. Frontiers Media S.A. 2022-12-07 /pmc/articles/PMC9767944/ /pubmed/36569850 http://dx.doi.org/10.3389/fimmu.2022.1074698 Text en Copyright © 2022 Ma and Zhang https://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
Ma, Chaoyu
Zhang, Nu
Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells
title Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells
title_full Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells
title_fullStr Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells
title_full_unstemmed Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells
title_short Lymphoid tissue residency: A key to understand Tcf-1(+)PD-1(+) T cells
title_sort lymphoid tissue residency: a key to understand tcf-1(+)pd-1(+) t cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9767944/
https://www.ncbi.nlm.nih.gov/pubmed/36569850
http://dx.doi.org/10.3389/fimmu.2022.1074698
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