Vascular Normalization as an Emerging Strategy to Enhance Cancer Immunotherapy

被引:525
作者
Huang, Yuhui
Goel, Shom
Duda, Dan G.
Fukumura, Dai
Jain, Rakesh K.
机构
[1] Massachusetts Gen Hosp, Dept Radiat Oncol, Edwin L Steele Lab Tumor Biol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
关键词
ENDOTHELIAL GROWTH-FACTOR; REGULATORY T-CELLS; TUMOR MICROENVIRONMENT; INHIBITOR; BLOCKADE; TOLERANCE; REVERSAL; SURVIVAL; EFFICACY; VACCINES;
D O I
10.1158/0008-5472.CAN-12-4354
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The recent approval of Provenge has brought new hope for anticancer vaccine therapies. However, the immunosuppressive tumor microenvironment seems to impair the efficacy of vaccine therapies. The abnormal tumor vasculature creates a hypoxic microenvironment that polarizes inflammatory cells toward immune suppression. Moreover, tumors systemically alter immune cells' proliferation, differentiation, and function via secretion of growth factors and cytokines. For example, VEGF, a major proangiogenic cytokine induced by hypoxia, plays a critical role in immunosuppression via these mechanisms. Hence, antiangiogenic treatment may be an effective modality to potentiate immunotherapy. Here, we discuss the local and systemic effects of VEGF on tumor immunity and propose a potentially translatable strategy to re-engineer the tumor-immune microenvironment and improve cancer immunotherapy by using lower "vascular normalizing" doses of antiangiogenic agents. Cancer Res; 73(10); 2943-8. (C) 2013 AACR.
引用
收藏
页码:2943 / 2948
页数:6
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