Pivotal roles of CD8+ T cells restricted by MHC class I-like molecules in autoimmune diseases

被引:5
作者
Das, Gobardhan [1 ]
Das, Jyoti
Eynott, Paul
Zhang, Yingyu
Bothwell, Alfred L. M.
Van Kaer, Luc
Shi, Yufang
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol Genet Microbiol & Immunol, Piscataway, NJ 08854 USA
[2] Sanofi Aventis, Dept Internal Med, Bridgewater, NJ 08807 USA
[3] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
[4] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37232 USA
关键词
D O I
10.1084/jem.20060936
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Unlike T cells restricted by major histocompatibility complex (MHC) class Ia or class II molecules, T cells restricted by MHC class I-like molecules demonstrate properties of both innate and adaptive immunity and are therefore considered innate-like lymphocytes (ILLs). ILLs are believed to have immunoregulatory functions, but their roles in autoimmunity and defense against infections remain elusive. To study the properties of ILLs, we generated mice expressing only MHC class I-like molecules by crossing CIITA-/with Kb(-/-)Db(-/-) mice. Surprisingly, these mice developed a lymphoproliferative syndrome and autoimmunity, most notably inflammatory bowel disease (IBD) and insulitis. The CD8(+) ILLs in these mice exhibit a constitutively activated phenotype, and depletion of these cells abolished the autoimmune disorders. In addition, adoptive transfer of CD8(+) ILLs from Kb(-/-)Db(-/-)CIITA(-/-) mice to Rag-1(-/-) pfn(-/-) mice also resulted in IBD and insulitis. These fi ndings provide direct evidence that CD8(+) ILLs are sufficient to initiate and mediate autoimmune diseases.
引用
收藏
页码:2603 / 2611
页数:9
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