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The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells
The literature surrounding KLRG1 has primarily focused on NK and CD8(+) T cells. However, there is evidence that the most suppressive Tregs express KLRG1. Until now, the role of KLRG1 on Tregs has been mostly overlooked and remains to be elucidated. Here we review the current literature on KLRG1 wit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098823/ https://www.ncbi.nlm.nih.gov/pubmed/35572605 http://dx.doi.org/10.3389/fimmu.2022.894508 |
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author | Borys, Samantha M. Bag, Arup K. Brossay, Laurent Adeegbe, Dennis O. |
author_facet | Borys, Samantha M. Bag, Arup K. Brossay, Laurent Adeegbe, Dennis O. |
author_sort | Borys, Samantha M. |
collection | PubMed |
description | The literature surrounding KLRG1 has primarily focused on NK and CD8(+) T cells. However, there is evidence that the most suppressive Tregs express KLRG1. Until now, the role of KLRG1 on Tregs has been mostly overlooked and remains to be elucidated. Here we review the current literature on KLRG1 with an emphasis on the KLRG1(+) Treg subset role during cancer development and autoimmunity. KLRG1 has been recently proposed as a new checkpoint inhibitor target, but these studies focused on the effects of KLRG1 blockade on effector cells. We propose that when designing anti-tumor therapies targeting KLRG1, the effects on both effector cells and Tregs will have to be considered. |
format | Online Article Text |
id | pubmed-9098823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90988232022-05-14 The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells Borys, Samantha M. Bag, Arup K. Brossay, Laurent Adeegbe, Dennis O. Front Immunol Immunology The literature surrounding KLRG1 has primarily focused on NK and CD8(+) T cells. However, there is evidence that the most suppressive Tregs express KLRG1. Until now, the role of KLRG1 on Tregs has been mostly overlooked and remains to be elucidated. Here we review the current literature on KLRG1 with an emphasis on the KLRG1(+) Treg subset role during cancer development and autoimmunity. KLRG1 has been recently proposed as a new checkpoint inhibitor target, but these studies focused on the effects of KLRG1 blockade on effector cells. We propose that when designing anti-tumor therapies targeting KLRG1, the effects on both effector cells and Tregs will have to be considered. Frontiers Media S.A. 2022-04-29 /pmc/articles/PMC9098823/ /pubmed/35572605 http://dx.doi.org/10.3389/fimmu.2022.894508 Text en Copyright © 2022 Borys, Bag, Brossay and Adeegbe 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 Borys, Samantha M. Bag, Arup K. Brossay, Laurent Adeegbe, Dennis O. The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells |
title | The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells |
title_full | The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells |
title_fullStr | The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells |
title_full_unstemmed | The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells |
title_short | The Yin and Yang of Targeting KLRG1(+) Tregs and Effector Cells |
title_sort | yin and yang of targeting klrg1(+) tregs and effector cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098823/ https://www.ncbi.nlm.nih.gov/pubmed/35572605 http://dx.doi.org/10.3389/fimmu.2022.894508 |
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