MDSC: Markers, development, states, and unaddressed complexity

被引:405
作者
Hegde, Samarth [1 ,2 ,3 ]
Leader, Andrew M. [1 ,2 ,3 ]
Merad, Miriam [1 ,2 ,3 ,4 ]
机构
[1] Icahn Sch Med Mt Sinai, Precis Immunol Inst, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Human Immune Monitoring Ctr, New York, NY 10029 USA
关键词
T-CELL-ACTIVATION; SUPPRESSOR-CELLS; MYELOID CELLS; HEMATOPOIETIC STEM; IMMUNE SUPPRESSION; MASS CYTOMETRY; IMMUNOSUPPRESSION; MONOCYTE; PROGENITORS; NEUTROPHILS;
D O I
10.1016/j.immuni.2021.04.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Myeloid-derived suppressor cells (MDSCs) are one of the most discussed biological entities in immunology. While the context and classification of this group of cells has evolved, MDSCs most commonly describe cells arising during chronic inflammation, especially late-stage cancers, and are defined by their T cell immunosuppressive functions. This MDSC concept has helped explain myeloid phenomena associated with disease outcome, but currently lacks clear definitions and a unifying framework across pathologies. Here, we propose such a framework to classify MDSCs as discrete cell states based on activation signals in myeloid populations leading to suppressive modes characterized by specific, measurable effects. Developing this level of knowledge of myeloid states across pathological conditions may ultimately transform how disparate diseases are grouped and treated.
引用
收藏
页码:875 / 884
页数:10
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