The IL-2/IL-2R system: from basic science to therapeutic applications to enhance immune regulation

被引:70
作者
Bayer, Allison L. [1 ,3 ]
Pugliese, Alberto [1 ,2 ,3 ]
Malek, Thomas R. [1 ,3 ]
机构
[1] Univ Miami, Dept Microbiol & Immunol, Miller Sch Med, Miami, FL 33101 USA
[2] Univ Miami, Dept Med, Miller Sch Med, Miami, FL 33101 USA
[3] Univ Miami, Diabet Res Inst, Miller Sch Med, Miami, FL 33101 USA
关键词
Treg cells; IL-2; Autoimmunity; Tolerance; Type; 1; diabetes; Insulin; T-CELLS; HUMAN THYMUS; DENDRITIC CELLS; DIFFERENTIAL EXPRESSION; LETHAL AUTOIMMUNITY; INSULIN EXPRESSION; PANCREATIC-ISLETS; GENE-EXPRESSION; CUTTING EDGE; DOUBLE-BLIND;
D O I
10.1007/s12026-013-8452-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-2 plays a critical role in the normal function of the immune system. A trophic factor for lymphocytes, IL-2 is required for mounting and sustaining adaptive T cell responses; however, IL-2 is also critical for immune regulation via its effects on regulatory T cells (Treg cells). Over the years, we have contributed to the understanding of the biology of IL-2 and its signaling through the IL-2 receptor and helped define the key role played by IL-2 in Treg development and function. Our data show that Treg cells have a heightened sensitivity to IL-2, which may create a therapeutic window to promote immune regulation by selective stimulation of Treg cells. We are now developing new efforts to translate this knowledge to the clinical arena, through our focused interest in Type 1 diabetes as a prototypic autoimmune disease. Specifically, we aim at developing IL-2-based therapeutic regimens and incorporate means to enhance antigen-specific Treg responses, for improved and more selective regulation of islet autoimmunity. In parallel, we are pursuing studies in preclinical models of autoimmunity and transplantation to define critical factors for successful adoptive Treg therapy and develop clinically applicable therapeutic protocols.
引用
收藏
页码:197 / 209
页数:13
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