Genetic control of the inflammatory T-cell response in regulatory T-cell deficient scurfy mice

被引:8
|
作者
Sharma, Rahul [1 ]
Ju, Shyr-Te [1 ]
机构
[1] Univ Virginia, Dept Med, Ctr Inflammat Immun & Regenerat Med, Charlottesville, VA 22908 USA
关键词
Multi-organ inflammation; Scurfy mice; Genetic regulation; BONE-MARROW-TRANSPLANTATION; IPEX SYNDROME; DISEASE; IMPINGE; MOUSE; IL-2; AUTOIMMUNITY; REPERTOIRE; MECHANISMS; EXPRESSION;
D O I
10.1016/j.clim.2010.04.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IPEX (Immunodysregulation, polyendocrinopathy, enteropathy, X-linked) syndrome is a rare, recessive disorder in patients with mutations in the foxp3 gene, the normal expression of which is required for the generation of functional regulatory T-cells. Scurfy mice also bear a mutation in the foxp3, and like IPEX patients, spontaneously develop multi-organ inflammation. As reviewed herein, breeding immune response genes into Scurfy mice has provided useful insight into how the inflammatory T-cell response is regulated in the absence of regulatory T-cells and post regulatory T-cell checkpoint. Of particular interest are those that preferentially affect the inflammatory T-cell response in an "apparent" organ-specific manner, implying that specific mechanisms of control exist for individual organs during multi-organ inflammation. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:162 / 169
页数:8
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