Activation of NK Cells and T Cells by NKG2D, a Receptor for Stress-Inducible MICA

被引:2455
作者
Bauer, Stefan [1 ,3 ]
Groh, Veronika [1 ]
Wu, Jun [2 ]
Steinle, Alexander [1 ]
Phillips, Joseph H. [2 ]
Lanier, Lewis L. [2 ]
Spies, Thomas [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1100 Fairview Ave North, Seattle, WA 98109 USA
[2] DNAX Res Inst Mol & Cellular Biol Inc, 901 Calif Ave, Palo Alto, CA 94304 USA
[3] Tech Univ Munich, Inst Microbiol, Trogerstr 32, D-81675 Munich, Germany
关键词
NATURAL-KILLER-CELLS; CLASS-I MOLECULES; INHIBITORY RECEPTOR; HLA-E; EXPRESSION; RECOGNITION; CLONES; SUPERFAMILY; LYMPHOCYTES; CD94/NKG2A;
D O I
10.1126/science.285.5428.727
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Stress-inducible MICA, a distant homolog of major histocompatibility complex (MHC) class I, functions as an antigen for gamma delta T cells and is frequently expressed in epithelial tumors. A receptor for MICA was detected on most gamma delta T cells, CD8(+) alpha beta T cells, and natural killer (NK) cells and was identified as NKG2D. Effector cells from all these subsets could be stimulated by ligation of NKG2D. Engagement of NKG2D activated cytolytic responses of gamma delta T cells and NK cells against transfectants and epithelial tumor cells expressing MICA. These results define an activating immunoreceptor-MHC ligand interaction that may promote antitumor NK and T cell responses.
引用
收藏
页码:2231 / 2233
页数:3
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