Cytokine-driven regulation of NK cell functions in tumor immunity: Role of the MICA-NKG2D system

被引:69
作者
Zwirner, Norberto W.
Fuertes, Mercedes B.
Girart, Maria Victoria
Domaica, Carolina I.
Rossi, Lucas E.
机构
[1] Hosp Clin Jose San Martin, Lab Inmunogenet, RA-1120 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Med, Dept Microbiol, RA-1053 Buenos Aires, DF, Argentina
关键词
MHC; NKG2D; NK cells; MICA; tumor;
D O I
10.1016/j.cytogfr.2007.01.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural killer (NK) cells are critical players during tumor growth control in immunocompetent hosts. These cells also establish a cross-talk with dendritic cells (DCs) and promote a Th1-mediated immunity. NKG2D is a pivotal receptor that directs the tumoricidal activity of NK cells through the recognition of a group of ligands such as MICA widely expressed on different tumors. Here we will review the most important tumor immune escape mechanisms that compromise the functionality of NKG2D and its cognate ligands, including TGF-beta secretion, tumor shedding of soluble MICA, and additional mechanisms that compromise the tumoricidal activity of NKG2D-expressing cells. Such mechanisms may also dampen the cross-talk between NK cells and DCs during the anti-tumor immune responses. Recent knowledge may lead to innovative approaches to promote efficient NK cell-mediated anti-tumor immune responses. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:159 / 170
页数:12
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