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α-1抗胰蛋白酶治疗自身免疫性疾病

Alpha-1 Antitrypsin Therapy for Autoimmune Disorders.

作者信息

Song Sihong

机构信息

Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville.

出版信息

Chronic Obstr Pulm Dis. 2018 Oct 5;5(4):289-301. doi: 10.15326/jcopdf.5.4.2018.0131.

Abstract

Autoimmune diseases are conditions caused by an over reactive immune system that attacks self-tissues and organs. Although the pathogenesis of autoimmune disease is complex and multi-factorial, inflammation is commonly involved. Therefore, anti-inflammatory therapies hold potential for the treatment of autoimmune diseases. However, long-term control of inflammation is challenging and most of the currently used drugs have side effects. Alpha-1 antitrypsin (AAT) is an anti-inflammatory protein with a well-known safety profile. The therapeutic potential of AAT has been tested in several autoimmune disease models. The first study using a recombinant adeno-associated viral (rAAV) vector showed that AAT gene transfer prevented the development of type 1 diabetes (T1D) in the non-obese diabetic (NOD) mouse model. Subsequent studies showed that treatment with AAT protein prevented and reversed type 1 diabetes. The beneficial effects of AAT treatment have also been observed in other autoimmune disease models such as rheumatoid arthritis and systemic lupus erythematosus. This paper reviews the therapeutic application of AAT and discusses possible mechanisms of action in various autoimmune diseases.

摘要

自身免疫性疾病是由过度活跃的免疫系统攻击自身组织和器官所引起的病症。尽管自身免疫性疾病的发病机制复杂且涉及多因素,但炎症通常与之相关。因此,抗炎疗法对自身免疫性疾病的治疗具有潜力。然而,长期控制炎症具有挑战性,并且目前使用的大多数药物都有副作用。α-1抗胰蛋白酶(AAT)是一种具有良好安全性记录的抗炎蛋白。AAT的治疗潜力已在多种自身免疫性疾病模型中得到测试。第一项使用重组腺相关病毒(rAAV)载体的研究表明,AAT基因转移可预防非肥胖糖尿病(NOD)小鼠模型中1型糖尿病(T1D)的发展。随后的研究表明,用AAT蛋白治疗可预防和逆转1型糖尿病。在其他自身免疫性疾病模型如类风湿性关节炎和系统性红斑狼疮中也观察到了AAT治疗的有益效果。本文综述了AAT的治疗应用,并讨论了其在各种自身免疫性疾病中的可能作用机制。

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