A new role for an old player: Do B cells unleash the self-reactive CD8+T cell storm necessary for the development of type 1 diabetes?

被引:24
作者
Marino, Eliana [1 ]
Grey, Shane T. [1 ]
机构
[1] Garvan Inst Med Res, Arthrit & Inflammat Program, Gene Therapy & Autoimmun Grp, Darlinghurst, NSW 2010, Australia
关键词
Autoimmunity; B cells; CD8+T cell; Diabetes;
D O I
10.1016/j.jaut.2008.04.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Type 1 diabetes mellitus is an autoimmune disease mediated by a selective immune-mediated destruction of the insulin containing beta cells within the pancreatic islets of Langerhans. T cells reactive to beta cell-derived antigens are critical for the pathogenesis of type 1 diabetes, indeed treatments that target T cells are currently in clinical trials. CD8+ T cells may play a particularly crucial role in the onset of hyperglycaemia, as they can mediate beta cell destruction late in the pathogenesis of diabetes. However, the precise steps by which beta cell-reactive CD8+ T cells are activated are poorly understood. In this review we speculate on the possibility that B cells are essential for the activation and expansion of pathogenic CD8+ T cells that cause final beta cell destruction, We also discuss the involvement of different B cell subsets in the aetiology of diabetes. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:301 / 305
页数:5
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