Neutrophil plasticity in the tumor microenvironment

被引:539
|
作者
Giese, Morgan A. [1 ]
Hind, Laurel E. [1 ]
Huttenlocher, Anna [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Med Microbiol & Immunol, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Pediat, Madison, WI USA
基金
美国国家卫生研究院;
关键词
SUPPRESSOR-CELLS; T-CELLS; IMMUNE SUPPRESSION; OVARIAN-CARCINOMA; ONCOSTATIN-M; ARGINASE; INFLAMMATION; POLARIZATION; METASTASIS; PHENOTYPE;
D O I
10.1182/blood-2018-11-844548
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neutrophils act as the body's first line of defense against infection and respond to diverse inflammatory cues, including cancer. Neutrophils display plasticity, with the ability to adapt their function in different inflammatory contexts. In the tumor microenvironment, neutrophils have varied functions and have been classified using different terms, including N1/N2 neutrophils, tumor-associated neutrophils, and polymorphonuclear neutrophil myeloid-derived suppressor cells (PMN-MDSCs). These populations of neutrophils are primarily defined by their functional phenotype, because few specific cell surface markers have been identified. In this review, we will discuss neutrophil polarization and plasticity and the function of proinflammatory/anti-inflammatory and protumor/antitumor neutrophils in the tumor microenvironment. We will also discuss how neutrophils with the ability to suppress T-cell activation, referred to by some as PMN-MDSCs, fit into this paradigm.
引用
收藏
页码:2159 / 2167
页数:9
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