T Regulatory Cells in Autoimmune Diabetes: Past Challenges, Future Prospects

被引:92
作者
Bluestone, Jeffrey A. [1 ]
Tang, Qizhi [1 ]
Sedwick, Caitlin E. [1 ]
机构
[1] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
关键词
Tregs; diabetes; autoimmunity; Foxp3;
D O I
10.1007/s10875-008-9242-z
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Accumulating evidence suggests that defective regulation is an essential underlying cause of autoimmunity. The development of type I diabetes in the NOD mouse strain it is a complex process that depends on a fine balance between pathogenic and regulatory pathways. Discussion We have utilized a series of transgenic and knockout mice to determine the relative importance of regulatory T cells and negative regulatory receptors on the development and progression of type I diabetes. Conclusion This review will focus on the origins and function of Treg in peripheral self-tolerance. We will summarize the role of Treg in preventing autoimmune diseases, with a particular focus on Type 1 Diabetes (T1D), and discuss the prospects for Treg-based therapies for autoimmune diseases.
引用
收藏
页码:677 / 684
页数:8
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