Regulation of autoimmune disease by natural killer T cells

被引:49
作者
Sharif, S
Arreaza, GA
Zucker, P
Mi, QS
Delovitch, TL
机构
[1] John P Robarts Res Inst, Autoimmun Diabet Grp, London, ON N6G 2V4, Canada
[2] Univ Western Ontario, Dept Microbiol & Immunol, London, ON N6A 5C1, Canada
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2002年 / 80卷 / 05期
基金
加拿大健康研究院;
关键词
CD1d; alpha-galactosylceramide; immunoregulatory cells; autoimmune type I diabetes; NOD;
D O I
10.1007/s00109-002-0332-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Natural killer T (NKT) cells express phenotypic characteristics shared by conventional natural killer cells and T cells, and reside in several primary and secondary lymphoid as well as nonlymphoid organs. Although these cells possess important effector functions in immunity against cancer and microbial pathogens, their immunoregulatory function has received much recent attention. There is convincing evidence to suggest a regulatory role for these cells in the control of susceptibility to autoimmune disease. NKT cells are reduced in number and function in autoimmune disease prone mice and humans. Studies conducted in mice have shown that transfer of NKT cells to disease-susceptible recipients prevents the development of autoimmune disease. The recent discovery that alpha-galactosylceramide, a glycolipid, can specifically target NKT cells expressing the invariant T cell receptor (TCR) to proliferate and produce an array of regulatory cytokines and chemokines has generated considerable interest to utilize these cells as targets of new therapeutic interventions for the immunoregulation of autoimmune disease.
引用
收藏
页码:290 / 300
页数:11
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