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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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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