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靶向干扰素-α:系统性红斑狼疮治疗的一种有前景的方法。

Targeting interferon-alpha: a promising approach for systemic lupus erythematosus therapy.

作者信息

Schmidt K N, Ouyang W

机构信息

Department of Immunology, Genentech Inc., San Francisco 94080, USA.

出版信息

Lupus. 2004;13(5):348-52. doi: 10.1191/0961203304lu1025oa.

Abstract

System lupus erythematosus (SLE) is an autoimmune disease with multicellular pathogeneic components. Recent studies suggest an important role for interferon-alpha (IFN) in the immunopathogenesis of SLE. Data demonstrating a correlation between IFN-alpha and SLE disease severity range from elevated IFN-alpha levels in patients' serum and induction of IFN-regulated genes in peripheral blood mononuclear cells, to drug induced lupus disease in hepatitis C or cancer patients treated with recombinant IFN-alpha. In addition, mouse models of lupus in which the IFNR is deleted fail to develop disease manifestations. Thus, targeting IFN-alpha promises to be therapeutically efficacious for SLE.

摘要

系统性红斑狼疮(SLE)是一种具有多细胞致病成分的自身免疫性疾病。最近的研究表明,α干扰素(IFN)在SLE的免疫发病机制中起重要作用。表明IFN-α与SLE疾病严重程度之间存在相关性的数据范围广泛,从患者血清中IFN-α水平升高以及外周血单个核细胞中IFN调节基因的诱导,到丙型肝炎或接受重组IFN-α治疗的癌症患者中药物性狼疮疾病。此外,缺失IFNR的狼疮小鼠模型未能出现疾病表现。因此,针对IFN-α有望对SLE具有治疗效果。

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