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Interferon regulatory factor 5 in human autoimmunity and murine models of autoimmune disease

机译:干扰素调节因子5在人类自身免疫和小鼠自身免疫性疾病的模型中

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摘要

Interferon regulatory factor 5 (IRF5) has been demonstrated as a key transcription factor of the immune system, playing important roles in modulating inflammatory immune responses in numerous cell types including dendritic cells, macrophages, and B cells. As well as driving the expression of type I interferon in antiviral responses, IRF5 is also crucial for driving macrophages toward a proinflammatory phenotype by regulating cytokine and chemokine expression and modulating B-cell maturity and antibody production. This review highlights the functional importance of IRF5 in a disease setting, by discussing polymorphic mutations at the human Irf5 locus that lead to susceptibility to systemic lupus erythematosus, rheumatoid arthritis, and inflammatory bowel disease. In concordance with this, we also discuss lessons in IRF5 functionality learned from murine in vivo models of autoimmune disease and inflammation and hypothesize that modulation of IRF5 activity and expression could provide potential therapeutic benefits in the clinic.
机译:干扰素调节因子5(IRF5)已被证明是免疫系统的关键转录因子,在调节包括树突状细胞,巨噬细胞和B细胞在内的多种细胞类型中的炎症性免疫应答中起着重要作用。除了在抗病毒反应中驱动I型干扰素的表达外,IRF5对于通过调节细胞因子和趋化因子的表达以及调节B细胞的成熟度和抗体产生,还可以将巨噬细胞驱动至促炎表型。这篇综述通过讨论人类Irf5基因座上的多态性突变,突出了IRF5在疾病中的功能重要性,这些突变导致易患系统性红斑狼疮,类风湿性关节炎和炎症性肠病。与此相应,我们还讨论了从小鼠自身免疫性疾病和炎症的体内模型中学到的IRF5功能方面的经验教训,并假设对IRF5活性和表达的调节可在临床上提供潜在的治疗益处。

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