Interferon regulatory factor signaling in autoimmune disease.

Interferon regulatory factor signaling in autoimmune disease.
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DOI:
10.1016/j.cyto.2017.02.006
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发表时间:
2017-10
期刊:
影响因子:
3.8
通讯作者:
Barnes BJ
Barnes BJ
中科院分区:
医学3区
文献类型:
--
作者:
Matta B;Song S;Li D;Barnes BJ

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干扰素调节因子(Interferon Regulatory Factor,IRFs)在病原体诱导的先天免疫应答和随后的适应性免疫应答中起着关键作用。因此,IRF信号传导的失调被认为有助于自身免疫性疾病的发病机制。事实上,许多鼠体内研究已经证明了在Irf缺陷小鼠中对特定自身免疫性疾病的保护或增强的易感性。然而,缺乏的是在来自自身免疫性疾病患者的原代免疫细胞中复制这些体内观察结果。这些类型的研究是必不可少的,因为大多数体内数据支持IRF在IRF缺陷小鼠中的保护作用,但IRF通常在患者免疫细胞中过表达。在这两个研究领域--小鼠和人类--都开始出现大量的工作。
Interferon regulatory factors (IRFs) play critical roles in pathogen-induced innate immune responses and the subsequent induction of adaptive immune response. Dysregulation of IRF signaling is therefore thought to contribute to autoimmune disease pathogenesis. Indeed, numerous murine in vivo studies have documented protection from or enhanced susceptibility to particular autoimmune diseases in Irf-deficient mice. What has been lacking, however, is replication of these in vivo observations in primary immune cells from patients with autoimmune disease. These types of studies are essential as the majority of in vivo data support a protective role for IRFs in Irf-deficient mice, yet IRFs are often found to be overexpressed in patient immune cells. A significant body of work is beginning to emerge from both of these areas of study – mouse and human.
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发表时间: 2009-02
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