Cross-talk between myeloid-derived suppressor cells (MDSC), macrophages, and dendritic cells enhances tumor-induced immune suppression

被引:431
|
作者
Ostrand-Rosenberg, Suzanne [1 ]
Sinha, Pratima [1 ]
Beury, Daniel W. [1 ]
Clements, Virginia K. [1 ]
机构
[1] Univ Maryland Baltimore Cty, Dept Biol Sci, Baltimore, MD 21250 USA
关键词
Tumor immunity; Immune escape; Tumor microenvironment; Tumor-associated macrophages; MHC CLASS-II; NATURAL-KILLER-CELLS; REGULATORY T-CELLS; HEPATOCELLULAR-CARCINOMA; BREAST-CANCER; BEARING HOST; DOWN-REGULATION; RECEPTOR; KAPPA-B; INFLAMMATION;
D O I
10.1016/j.semcancer.2012.01.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The tumor microenvironment is a complex milieu of tumor and host cells. Host cells can include tumor-reactive T cells capable of killing tumor cells. However, more frequently the tumor and host components interact to generate a highly immune suppressive environment that frustrates T cell cytotoxicity and promotes tumor progression through a variety of immune and non-immune mechanisms. Myeloid-derived suppressor cells (MDSC) are a major host component contributing to the immune suppressive environment. In addition to their inherent immune suppressive function, MDSC amplify the immune suppressive activity of macrophages and dendritic cells via cross-talk This article will review the cell-cell interactions used by MDSC to inhibit anti-tumor immunity and promote progression, and the role of inflammation in promoting cross-talk between MDSC and other cells in the tumor microenvironment. (C) 2012 Published by Elsevier Ltd.
引用
收藏
页码:275 / 281
页数:7
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