Targeting veGF/veGFR to Modulate Antitumor immunity

被引:473
作者
Yang, Ju [1 ]
Yan, Jing [1 ]
Liu, Baorui [1 ]
机构
[1] Nanjing Univ, Clin Canc Inst, Med Sch, Drum Tower Hosp,Comprehens Canc Ctr, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
vascular endothelial growth factor; tumor; angiogenesis; immune; T cells; ENDOTHELIAL GROWTH-FACTOR; REGULATORY T-CELLS; ANTI-VEGF THERAPY; DIRECTLY SUPPRESSES ACTIVATION; DENDRITIC CELLS; ANTIANGIOGENIC THERAPY; NITRIC-OXIDE; VASCULAR NORMALIZATION; TUMOR MICROENVIRONMENT; ADHESION MOLECULE;
D O I
10.3389/fimmu.2018.00978
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In addition to the crucial role in promoting the growth of tumor vessels, vascular endothelial growth factor (VEGF) is also immunosuppressive. VEGF can inhibit the function of T cells, increase the recruitment of regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs), and hinder the differentiation and activation of dendritic cells (DCs). Recent studies have investigated the role of antiangiogenic agents in antitumor immunity, especially in recent 3 years. Therefore, it is necessary to update the role of targeting VEGF/VEGFR in antitumor immunity. In this review, we focus on the latest clinical and preclinical findings on the modulatory role of antiangiogenic agents targeting VEGF/VEGFR in immune cells, including effector T cells, Tregs, MDSCs, DCs, tumor-associated macrophages, and mast cells. Our review will be potentially helpful for the development of combinations of angiogenesis inhibitors with immunological modulators.
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页数:9
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