Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects

Abstract Regulatory T cells (Tregs) characterized by the expression of the master transcription factor forkhead box protein p3 (Foxp3) suppress anticancer immunity, thereby hindering protective immunosurveillance of tumours and hampering effective antitumour immune responses in tumour-bearing hosts,...

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Main Authors: Chunxiao Li, Ping Jiang, Shuhua Wei, Xiaofei Xu, Junjie Wang
Format: Article
Language:English
Published: BMC 2020-07-01
Series:Molecular Cancer
Online Access:http://link.springer.com/article/10.1186/s12943-020-01234-1
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spelling doaj-93b8e341f8904da7b7eb90d11e94279c2020-11-25T03:20:52ZengBMCMolecular Cancer1476-45982020-07-0119112310.1186/s12943-020-01234-1Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospectsChunxiao Li0Ping Jiang1Shuhua Wei2Xiaofei Xu3Junjie Wang4Department of Radiation Oncology, Peking University Third HospitalDepartment of Radiation Oncology, Peking University Third HospitalDepartment of Radiation Oncology, Peking University Third HospitalCenter for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third HospitalDepartment of Radiation Oncology, Peking University Third HospitalAbstract Regulatory T cells (Tregs) characterized by the expression of the master transcription factor forkhead box protein p3 (Foxp3) suppress anticancer immunity, thereby hindering protective immunosurveillance of tumours and hampering effective antitumour immune responses in tumour-bearing hosts, constitute a current research hotspot in the field. However, Tregs are also essential for the maintenance of the immune tolerance of the body and share many molecular signalling pathways with conventional T cells, including cytotoxic T cells, the primary mediators of tumour immunity. Hence, the inability to specifically target and neutralize Tregs in the tumour microenvironment without globally compromising self-tolerance poses a significant challenge. Here, we review recent advances in characterizing tumour-infiltrating Tregs with a focus on the functional roles of costimulatory and inhibitory receptors in Tregs, evaluate their potential as clinical targets, and systematically summarize their roles in potential treatment strategies. Also, we propose modalities to integrate our increasing knowledge on Tregs phenotype and function for the rational design of checkpoint inhibitor-based combination therapies. Finally, we propose possible treatment strategies that can be used to develop Treg-targeted therapies.http://link.springer.com/article/10.1186/s12943-020-01234-1
collection DOAJ
language English
format Article
sources DOAJ
author Chunxiao Li
Ping Jiang
Shuhua Wei
Xiaofei Xu
Junjie Wang
spellingShingle Chunxiao Li
Ping Jiang
Shuhua Wei
Xiaofei Xu
Junjie Wang
Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
Molecular Cancer
author_facet Chunxiao Li
Ping Jiang
Shuhua Wei
Xiaofei Xu
Junjie Wang
author_sort Chunxiao Li
title Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
title_short Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
title_full Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
title_fullStr Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
title_full_unstemmed Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
title_sort regulatory t cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
publisher BMC
series Molecular Cancer
issn 1476-4598
publishDate 2020-07-01
description Abstract Regulatory T cells (Tregs) characterized by the expression of the master transcription factor forkhead box protein p3 (Foxp3) suppress anticancer immunity, thereby hindering protective immunosurveillance of tumours and hampering effective antitumour immune responses in tumour-bearing hosts, constitute a current research hotspot in the field. However, Tregs are also essential for the maintenance of the immune tolerance of the body and share many molecular signalling pathways with conventional T cells, including cytotoxic T cells, the primary mediators of tumour immunity. Hence, the inability to specifically target and neutralize Tregs in the tumour microenvironment without globally compromising self-tolerance poses a significant challenge. Here, we review recent advances in characterizing tumour-infiltrating Tregs with a focus on the functional roles of costimulatory and inhibitory receptors in Tregs, evaluate their potential as clinical targets, and systematically summarize their roles in potential treatment strategies. Also, we propose modalities to integrate our increasing knowledge on Tregs phenotype and function for the rational design of checkpoint inhibitor-based combination therapies. Finally, we propose possible treatment strategies that can be used to develop Treg-targeted therapies.
url http://link.springer.com/article/10.1186/s12943-020-01234-1
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