Regulation of regulatory T cells in cancer

被引:54
作者
Stockis, Julie [1 ]
Roychoudhuri, Rahul [2 ]
Halim, Timotheus Y. F. [1 ]
机构
[1] Univ Cambridge, CRUK Cambridge Inst, Robinson Way, Cambridge CB2 0RE, England
[2] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
cancer; chemokine; chemokine receptors; cytokines; cytokine receptors; regulatory T cells; tumour immunology; TUMOR-INFILTRATING LYMPHOCYTES; CHEMOKINE RECEPTOR CCR4; DENDRITIC CELLS; IMMUNE PRIVILEGE; CUTTING EDGE; NEUROPILIN; FOXP3; LOCUS; ICOS-LIGAND; TGF-BETA; EXPRESSION;
D O I
10.1111/imm.13064
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The inflammatory response to transformed cells forms the cornerstone of natural or therapeutically induced protective immunity to cancer. Regulatory T (Treg) cells are known for their critical role in suppressing inflammation, and therefore can antagonize effective anti-cancer immune responses. As such, Treg cells can play detrimental roles in tumour progression and in the response to both conventional and immune-based cancer therapies. Recent advances in our understanding of Treg cells reveal complex niche-specific regulatory programmes and functions, which are likely to extrapolate to cancer. The regulation of Treg cells is reliant on upstream cues from haematopoietic and non-immune cells, which dictates their genetic, epigenetic and downstream functional programmes. In this review we will discuss how Treg cells are themselves regulated in normal and transformed tissues, and the implications of this cross talk on tumour growth.
引用
收藏
页码:219 / 231
页数:13
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