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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.
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页码:162 / 169
页数:8
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