Deciphering and Reversing Tumor Immune Suppression

被引:497
|
作者
Motz, Greg T. [1 ]
Coukos, George [1 ,2 ,3 ]
机构
[1] Univ Penn, Sch Med, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA
[2] Univ Lausanne, Ludwig Ctr Canc Res, CH-1066 Epalinges, Switzerland
[3] Univ Lausanne, Dept Oncol, CH-1015 Lausanne, Switzerland
基金
美国国家卫生研究院;
关键词
ENDOTHELIAL GROWTH-FACTOR; REGULATORY T-CELLS; PLASMACYTOID DENDRITIC CELLS; LONG-TERM SURVIVAL; ANTI-VEGF THERAPY; MHC CLASS-I; NITRIC-OXIDE; OVARIAN-CARCINOMA; INDOLEAMINE 2,3-DIOXYGENASE; CHEMOKINE EXPRESSION;
D O I
10.1016/j.immuni.2013.07.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Generating an anti-tumor immune response is a multi-step process that is executed by effector T cells that can recognize and kill tumor targets. However, tumors employ multiple strategies to attenuate the effectiveness of T-cell-mediated attack. They achieve this by interfering with nearly every step required for effective immunity, from deregulation of antigen-presenting cells to establishment of a physical barrier at the vasculature that prevents homing of effector tumor-rejecting cells and the suppression of effector lymphocytes through the recruitment and activation of immunosuppressive cells such as myeloid-derived suppressor cells, tolerogenic monocytes, and T regulatory cells. Here, we review the ways in which tumors exert immune suppression and highlight the new therapies that seek to reverse this phenomenon and promote anti-tumor immunity. Understanding anti-tumor immunity, and how it becomes disabled by tumors, will ultimately lead to improved immune therapies and prolonged survival of patients.
引用
收藏
页码:61 / 73
页数:13
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