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Tregs: Where We Are and What Comes Next?
Regulatory T cells are usually recognized as a specialized subset of CD4(+) T cells functioning in establishment and maintenance of immune tolerance. Meanwhile, there is emerging evidence that regulatory T cells (Tregs) are also present in various non-lymphoid tissues, and that they have unique phen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705554/ https://www.ncbi.nlm.nih.gov/pubmed/29225597 http://dx.doi.org/10.3389/fimmu.2017.01578 |
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author | Zhao, Hai Liao, Xuelian Kang, Yan |
author_facet | Zhao, Hai Liao, Xuelian Kang, Yan |
author_sort | Zhao, Hai |
collection | PubMed |
description | Regulatory T cells are usually recognized as a specialized subset of CD4(+) T cells functioning in establishment and maintenance of immune tolerance. Meanwhile, there is emerging evidence that regulatory T cells (Tregs) are also present in various non-lymphoid tissues, and that they have unique phenotypes credited with activities distinct from regulatory function. Their development and function have been described in plenty of manuscripts in the past two decades. However, with the deepening of research in recent years, emerging evidence revealed some novel mechanisms about how Tregs exert their activities. First, we discuss the expanding family of regulatory lymphocytes briefly and then, try to interpret how fork-head box P3 (Foxp3), a master regulator of the regulatory pathway in the development and function of regulatory T cells, functions. Subsequently, another part of our focus is varieties of tissue Tregs. Next, we primarily discuss recent research on how Tregs work and their faceted functions in terms of soluble mediators, functional proteins, and inhibitory receptors. In particular, unless otherwise noted, the term “Treg” is used here to refer specially to the “CD4(+)CD25(+)Foxp3(+”) regulatory cells. |
format | Online Article Text |
id | pubmed-5705554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57055542017-12-08 Tregs: Where We Are and What Comes Next? Zhao, Hai Liao, Xuelian Kang, Yan Front Immunol Immunology Regulatory T cells are usually recognized as a specialized subset of CD4(+) T cells functioning in establishment and maintenance of immune tolerance. Meanwhile, there is emerging evidence that regulatory T cells (Tregs) are also present in various non-lymphoid tissues, and that they have unique phenotypes credited with activities distinct from regulatory function. Their development and function have been described in plenty of manuscripts in the past two decades. However, with the deepening of research in recent years, emerging evidence revealed some novel mechanisms about how Tregs exert their activities. First, we discuss the expanding family of regulatory lymphocytes briefly and then, try to interpret how fork-head box P3 (Foxp3), a master regulator of the regulatory pathway in the development and function of regulatory T cells, functions. Subsequently, another part of our focus is varieties of tissue Tregs. Next, we primarily discuss recent research on how Tregs work and their faceted functions in terms of soluble mediators, functional proteins, and inhibitory receptors. In particular, unless otherwise noted, the term “Treg” is used here to refer specially to the “CD4(+)CD25(+)Foxp3(+”) regulatory cells. Frontiers Media S.A. 2017-11-24 /pmc/articles/PMC5705554/ /pubmed/29225597 http://dx.doi.org/10.3389/fimmu.2017.01578 Text en Copyright © 2017 Zhao, Liao and Kang. 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) or licensor 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 Zhao, Hai Liao, Xuelian Kang, Yan Tregs: Where We Are and What Comes Next? |
title | Tregs: Where We Are and What Comes Next? |
title_full | Tregs: Where We Are and What Comes Next? |
title_fullStr | Tregs: Where We Are and What Comes Next? |
title_full_unstemmed | Tregs: Where We Are and What Comes Next? |
title_short | Tregs: Where We Are and What Comes Next? |
title_sort | tregs: where we are and what comes next? |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705554/ https://www.ncbi.nlm.nih.gov/pubmed/29225597 http://dx.doi.org/10.3389/fimmu.2017.01578 |
work_keys_str_mv | AT zhaohai tregswhereweareandwhatcomesnext AT liaoxuelian tregswhereweareandwhatcomesnext AT kangyan tregswhereweareandwhatcomesnext |