The effect of anti-angiogenic drugs on regulatory T cells in the tumor microenvironment

被引:21
|
作者
Hu, Chenxi [1 ]
Jiang, Xiaodong [1 ]
机构
[1] Xuzhou Med Univ, Dept Oncol, Tumor Lab, Affiliated Lianyungang Hosp, 182 Tongguan Rd, Lianyungang 222002, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Anti-angiogenics; Tumor microenvironment; Regulatory T cells; DENDRITIC CELLS; ANTIANGIOGENIC THERAPY; DIFFERENTIAL ROLES; VEGF THERAPY; CANCER; GROWTH; SUPPRESSION; RECRUITMENT; SURVIVAL; INFILTRATION;
D O I
10.1016/j.biopha.2017.01.051
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A benefit of anti-angiogenic drugs is improved tumor immune tolerance. Regulatory T cells (Tregs) in the tumor microenvironment mediate tumor immune tolerance and anti-angiogenic drugs not only indirectly affect Tregs via dendritic cells (DCs) and myeloid-derived suppressor cells (MDSCs) but they can also act directly on Tregs causing immunosuppression. Specifically, these drugs may induce differentiation and chemotaxis and reduce the number and function of Tregs by targeting vascular endothelial growth factor receptor 2 (VEGFR-2) and neuropilin-1 (NRP-1) on the cell surface. Recently, anti-angiogenic drugs have been documented to promote a new way of thinking about tumor immunotherapy: clinical application of Tregs and related immunosuppressive molecules may be promising targets for synergistic tumor immunotherapy. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:134 / 137
页数:4
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