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依那西普——肿瘤坏死因子受体与IgG1 Fc融合蛋白:它与其他肿瘤坏死因子阻滞剂有何不同?

Etanercept - TNF receptor and IgG1 Fc fusion protein: is it different from other TNF blockers?

作者信息

Marotte Hubert, Cimaz Rolando

机构信息

Hôpital Nord, CHU de Saint-Etienne, Department of Rheumatology , Saint-Etienne , France

出版信息

Expert Opin Biol Ther. 2014 May;14(5):569-72. doi: 10.1517/14712598.2014.896334. Epub 2014 Mar 10.

Abstract

TNF blockers have been available to treat various inflammatory disorders since more than a decade. T cells and macrophages mainly express TNF and activate many cells through two types of receptors. Pharmaceutical companies developed two types of TNF blockers: soluble receptors and monoclonal antibodies. Understanding of differences of structure and function can explain divergence of efficacy or side effects. Etanercept has the best retention rate in rheumatic diseases, but is less or not effective in granulomatous diseases, such as inflammatory bowel diseases or uveitis. However, etanercept induces less tuberculosis infections than anti-TNF blocker monoclonal antibodies.

摘要

十多年来,肿瘤坏死因子(TNF)阻滞剂一直用于治疗各种炎症性疾病。T细胞和巨噬细胞主要表达TNF,并通过两种类型的受体激活许多细胞。制药公司开发了两种类型的TNF阻滞剂:可溶性受体和单克隆抗体。了解其结构和功能的差异可以解释疗效或副作用的差异。依那西普在风湿性疾病中的保留率最高,但对肉芽肿性疾病(如炎症性肠病或葡萄膜炎)疗效较低或无效。然而,依那西普引起的结核感染比抗TNF阻滞剂单克隆抗体少。

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