Regulation of antitumour immunity by CD1d-restricted NKT cells

被引:55
|
作者
Swann, J
Crowe, NY
Hayakawa, Y
Godfrey, DI
Smyth, MJ
机构
[1] Peter MacCallum Canc Ctr, Trescowthick Labs, Canc Immunol Program, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
来源
IMMUNOLOGY AND CELL BIOLOGY | 2004年 / 82卷 / 03期
关键词
D O I
10.1111/j.1440-1711.2004.01254.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An understanding of the complex interactions occurring between tumours and the immune system is a prerequisite for the rational design of effective cancer immunotherapies. To date, attention has focused mainly on the role the adaptive immune system plays in controlling tumourigenesis, with conventional T cells, which recognize peptide antigens presented by classical MHC molecules, coming under close scrutiny. Accumulating reports now suggest that an additional T-cell subset, known as CD1d-restricted natural killer T (NKT) cells, also plays a pivotal role in modulating antitumour responses. Found in both humans and mice, CD1d-restricted NKT cells are a highly specialized cell type that, in contrast to conventional T cells, recognize lipid/glycolipid antigens presented by the non-classical MHC molecule CD1d. Several features of NKT cells, including their ability to rapidly produce large quantities of cytokines upon primary stimulation, make them ideal targets for developing anticancer immunotherapies. This intriguing cell type is the focus of this review.
引用
收藏
页码:323 / 331
页数:9
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