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系统性硬化症治疗的最新进展

Recent advances in the treatment of systemic sclerosis.

作者信息

Bournia Vasiliki Kalliopi K, Vlachoyiannopoulos Panayiotis G, Selmi Carlo, Moutsopoulos Haralampos M, Gershwin M Eric

机构信息

Department of Pathophysiology, Medical School, National University of Athens, Athens, Greece.

出版信息

Clin Rev Allergy Immunol. 2009 Jun;36(2-3):176-200. doi: 10.1007/s12016-008-8114-x.

Abstract

Systemic sclerosis (SSc) is a chronic autoimmune disease with clinical manifestations resulting from immune activation, fibrosis development, and damage of small blood vessels. Our aim was to critically illustrate the available data on the new treatments proposed for SSc to provide a clinically oriented overview of the current evidence. PubMed was used for literature search using "scleroderma" and "therapy" to identify all articles published on indexed journals between 1972 and 2008. The search was limited to publications in English and produced a total of 3,441 references, which included 735 review articles. These citations were then screened for articles dealing with the most recent therapy options for SSc, and 214 articles were selected for evaluation and discussion. Methotrexate, cyclophosphamide, calcium channel blockers, angiotensin converting enzyme inhibitors, prostacyclin analogues, D-penicillamine, and extracorporeal photopheresis are the most widely studied treatments for SSc and were considered as practiced treatments. Other therapeutic approaches have been developed more recently and include endothelin receptor antagonists and phosphodiesterase-5 inhibitors for pulmonary arterial hypertension and peripheral vascular disease. High-dose immunosuppression and stem cell transplantation constitute a promising treatment and data from randomized controlled trials are awaited. Intravenous gamma globulins, mycophenolate mophetil, collagen tolerance induction, rituximab, fluoxetine, pirfenidone, relaxin, halofuginone, anti-TGF-beta antibodies, and tyrosine kinase inhibitors awaits more solid data. The clinical management of patients with SSc remains a challenge and currently involves practiced and newly proposed therapeutic approaches. The disease pleiomorphism poses numerous difficulties to determine ideal outcomes to be used in clinical trials.

摘要

系统性硬化症(SSc)是一种慢性自身免疫性疾病,其临床表现源于免疫激活、纤维化发展以及小血管损伤。我们的目的是批判性地阐述针对SSc提出的新治疗方法的现有数据,以提供一个以临床为导向的当前证据概述。使用PubMed进行文献检索,检索词为“硬皮病”和“治疗”,以识别1972年至2008年间发表在索引期刊上的所有文章。检索仅限于英文出版物,共产生3441条参考文献,其中包括735篇综述文章。然后对这些引用文献进行筛选,以查找涉及SSc最新治疗选择的文章,共选择214篇文章进行评估和讨论。甲氨蝶呤、环磷酰胺、钙通道阻滞剂、血管紧张素转换酶抑制剂、前列环素类似物、D-青霉胺和体外光化学疗法是针对SSc研究最广泛的治疗方法,被视为常用治疗方法。其他治疗方法是最近才开发出来的,包括用于肺动脉高压和外周血管疾病的内皮素受体拮抗剂和磷酸二酯酶-5抑制剂。大剂量免疫抑制和干细胞移植是一种有前景的治疗方法,目前正在等待随机对照试验的数据。静脉注射丙种球蛋白、霉酚酸酯、胶原耐受性诱导、利妥昔单抗、氟西汀、吡非尼酮、松弛素、常山酮、抗转化生长因子-β抗体和酪氨酸激酶抑制剂等还需要更多确凿的数据。SSc患者的临床管理仍然是一项挑战,目前涉及常用和新提出的治疗方法。疾病的多形性给确定临床试验中使用的理想结果带来了许多困难。

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