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叉头框蛋白P3:免疫缺陷与自身免疫性疾病之间的遗传联系。

FoxP3: a genetic link between immunodeficiency and autoimmune diseases.

作者信息

Chang Xing, Zheng Pan, Liu Yang

机构信息

Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, 1645 Neil Avenue, 129 Hamilton Hall, Columbus, OH 43210, USA.

出版信息

Autoimmun Rev. 2006 Jul;5(6):399-402. doi: 10.1016/j.autrev.2005.10.008. Epub 2005 Dec 7.

Abstract

It has long been observed that patients with autoimmune diseases also have immune deficiency. How these two opposite extremes of immunity can be found in the same individual is largely unclear. Here we review the evidence that a FoxP3 defect may provide a critical link between autoimmunity and immune deficiency. Disruption of FoxP3 results in severe autoimmune syndromes in both human and mice. Bone marrow chimera experiments indicate that FoxP3 defects in both hematopoietic and non-hematopoietic cells are required for the development of severe autoimmune disease. FoxP3 mutation in the hematopoietic cells impairs the development of regulatory T cells (Treg). Our data demonstrate that the mutation in non-hematopoietic cells results in deficient thymopoiesis. Defective T cell production may be an underlying cause of T cell hyperproliferation, which together with Treg defects, may lead to fatal autoimmune disease in mouse and man.

摘要

长期以来人们一直观察到,自身免疫性疾病患者也存在免疫缺陷。目前尚不清楚在同一个体中如何会出现这两种截然相反的免疫状态。在此,我们综述了一些证据,这些证据表明FoxP3缺陷可能是自身免疫与免疫缺陷之间的关键联系。FoxP3的破坏在人类和小鼠中都会导致严重的自身免疫综合征。骨髓嵌合体实验表明,造血细胞和非造血细胞中的FoxP3缺陷都是严重自身免疫性疾病发生所必需的。造血细胞中的FoxP3突变会损害调节性T细胞(Treg)的发育。我们的数据表明,非造血细胞中的突变会导致胸腺生成不足。有缺陷的T细胞生成可能是T细胞过度增殖的一个潜在原因,这与Treg缺陷一起,可能导致小鼠和人类发生致命的自身免疫性疾病。

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