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Cross-talk between myeloid-derived suppressor cells (MDSC), macrophages, and dendritic cells enhances tumor-induced immune suppression
被引:433
|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.
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页码:275 / 281
页数:7
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