The Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, Nanjing, China.
Front Immunol. 2018 May 3;9:978. doi: 10.3389/fimmu.2018.00978. eCollection 2018.
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.
除了在促进肿瘤血管生长中发挥关键作用外,血管内皮生长因子(VEGF)也是一种免疫抑制因子。VEGF 可以抑制 T 细胞的功能,增加调节性 T 细胞(Tregs)和髓系来源的抑制细胞(MDSCs)的募集,并阻碍树突状细胞(DCs)的分化和激活。最近的研究调查了抗血管生成药物在抗肿瘤免疫中的作用,特别是在最近 3 年。因此,有必要更新针对 VEGF/VEGFR 在抗肿瘤免疫中的作用。在这篇综述中,我们重点介绍了针对 VEGF/VEGFR 的抗血管生成药物在免疫细胞(包括效应 T 细胞、Tregs、MDSCs、DCs、肿瘤相关巨噬细胞和肥大细胞)中调节作用的最新临床和临床前发现。我们的综述可能有助于开发血管生成抑制剂与免疫调节剂的联合疗法。