Molecular mechanisms regulating myeloid-derived suppressor cell differentiation and function

被引:678
作者
Condamine, Thomas [1 ]
Gabrilovich, Dmitry I. [1 ,2 ]
机构
[1] Univ S Florida, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Oncol Sci, Tampa, FL 33612 USA
关键词
TUMOR-BEARING MICE; T-CELLS; CANCER-PATIENTS; ARGINASE-I; IMMUNOSUPPRESSIVE ACTIVITY; EMERGENCY GRANULOPOIESIS; INFLAMMATORY MONOCYTES; PERIPHERAL-BLOOD; IMMUNE-RESPONSES; ACTIVATION;
D O I
10.1016/j.it.2010.10.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Myeloid-derived suppressor cells (MDSCs) are one of the main cell populations responsible for regulating immune responses. MDSCs accumulate during tumor progression, autoimmunity, chronic infection and other pathological conditions, and can potently suppress T cell function. Recent studies have demonstrated the ability of MDSCs to modulate the activity of NK and myeloid cells and have implicated MDSCs in the induction of regulatory T cells. Here, we discuss recent findings that describe the molecular mechanisms that regulate the expansion and function of MDSCs, as well as recent attempts to use MDSCs in cell therapy for different pathologic conditions.
引用
收藏
页码:19 / 25
页数:7
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