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KLRG1 restricts memory T cell antitumor immunity

Killer cell lectin-like receptor subfamily G member 1 (KLRG1) has been found on human memory T lymphocytes. However, the roles of KLRG1 on human T cells especially in tumor microenvironment have not been fully understood. Our results showed KLRG1 expression on T cells significantly increased in tumo...

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Detalles Bibliográficos
Autores principales: Li, Lei, Wan, Shanshan, Tao, Kaixiong, Wang, Guobin, Zhao, Ende
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308681/
https://www.ncbi.nlm.nih.gov/pubmed/27557510
http://dx.doi.org/10.18632/oncotarget.11430
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author Li, Lei
Wan, Shanshan
Tao, Kaixiong
Wang, Guobin
Zhao, Ende
author_facet Li, Lei
Wan, Shanshan
Tao, Kaixiong
Wang, Guobin
Zhao, Ende
author_sort Li, Lei
collection PubMed
description Killer cell lectin-like receptor subfamily G member 1 (KLRG1) has been found on human memory T lymphocytes. However, the roles of KLRG1 on human T cells especially in tumor microenvironment have not been fully understood. Our results showed KLRG1 expression on T cells significantly increased in tumor microenvironment. KLRG1(+) T cells exhibited poor proliferative capacity with decreased effector cytokine production. Meanwhile, KLRG1(+) T cells expressed abundant pro-inflammatory cytokines and demonstrated high level of Foxp3 expression. KLRG1(+) T cells showed decreased expression of miRNA-101 and higher expression of CtBP2. Our results indicated KLRG1 might contribute to the impaired antitumor immunity of memory T cells in tumor microenvironment. Thus, repressing KLRG1 on human memory T cells might be a novel therapeutics against cancer.
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spelling pubmed-53086812017-03-09 KLRG1 restricts memory T cell antitumor immunity Li, Lei Wan, Shanshan Tao, Kaixiong Wang, Guobin Zhao, Ende Oncotarget Research Paper Killer cell lectin-like receptor subfamily G member 1 (KLRG1) has been found on human memory T lymphocytes. However, the roles of KLRG1 on human T cells especially in tumor microenvironment have not been fully understood. Our results showed KLRG1 expression on T cells significantly increased in tumor microenvironment. KLRG1(+) T cells exhibited poor proliferative capacity with decreased effector cytokine production. Meanwhile, KLRG1(+) T cells expressed abundant pro-inflammatory cytokines and demonstrated high level of Foxp3 expression. KLRG1(+) T cells showed decreased expression of miRNA-101 and higher expression of CtBP2. Our results indicated KLRG1 might contribute to the impaired antitumor immunity of memory T cells in tumor microenvironment. Thus, repressing KLRG1 on human memory T cells might be a novel therapeutics against cancer. Impact Journals LLC 2016-08-20 /pmc/articles/PMC5308681/ /pubmed/27557510 http://dx.doi.org/10.18632/oncotarget.11430 Text en Copyright: © 2016 Li et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Li, Lei
Wan, Shanshan
Tao, Kaixiong
Wang, Guobin
Zhao, Ende
KLRG1 restricts memory T cell antitumor immunity
title KLRG1 restricts memory T cell antitumor immunity
title_full KLRG1 restricts memory T cell antitumor immunity
title_fullStr KLRG1 restricts memory T cell antitumor immunity
title_full_unstemmed KLRG1 restricts memory T cell antitumor immunity
title_short KLRG1 restricts memory T cell antitumor immunity
title_sort klrg1 restricts memory t cell antitumor immunity
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308681/
https://www.ncbi.nlm.nih.gov/pubmed/27557510
http://dx.doi.org/10.18632/oncotarget.11430
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