NKG2D ligands: unconventional MHC class I-like molecules exploited by viruses and cancer
被引:131
作者:
Cerwenka, A
论文数: 0引用数: 0
h-index: 0
机构:DKFZ, German Canc Ctr, D-69120 Heidelberg, Germany
Cerwenka, A
Lanier, LL
论文数: 0引用数: 0
h-index: 0
机构:DKFZ, German Canc Ctr, D-69120 Heidelberg, Germany
Lanier, LL
机构:
[1] DKFZ, German Canc Ctr, D-69120 Heidelberg, Germany
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[3] Canc Res Inst, San Francisco, CA 94143 USA
来源:
TISSUE ANTIGENS
|
2003年
/
61卷
/
05期
关键词:
innate immunity;
NK cells;
NKG2D;
RAE-1;
D O I:
10.1034/j.1399-0039.2003.00070.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Our best teachers in revealing the importance of immune pathways are viruses and cancers that have subverted the most prominent pathways to escape from immune recognition. Viruses and cancer impair antigen presentation by classical MHC class I to escape adaptive immunity. The activating receptor NKG2D and its MHC class I-like ligands are other recently defined innate and adaptive immune pathways exploited by viruses and cancer. This review discusses recent advances in the understanding of how NKG2D, expressed on innate immune cells including natural killer cells, gammadelta(+) T cells and macrophages, and adaptive immune cells such as CD8(+) T cells, recognize stress-induced, MHC class I-like, self-ligands. Moreover, we describe how viruses and cancer have developed strategies to evade this recognition pathway.