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变应性肉芽肿性血管炎的治疗:缓解诱导及静脉注射免疫球蛋白治疗的疗效

Treatment for Churg-Strauss syndrome: induction of remission and efficacy of intravenous immunoglobulin therapy.

作者信息

Taniguchi Masami, Tsurikisawa Naomi, Higashi Noritaka, Saito Hiroshi, Mita Haruhisa, Mori Akio, Sakakibara Hiroki, Akiyama Kazuo

机构信息

National Hospital Organization, Sagamihara National Hospital, Kanagawa, Japan.

出版信息

Allergol Int. 2007 Jun;56(2):97-103. doi: 10.2332/allergolint.R-07-142. Epub 2007 May 1.

Abstract

Churg-Strauss syndrome (CSS) is characterized by the presence of asthma, eosinophilia, and small-vessel vasculitis with granuloma. It is a distinct entity, as determined from all classifications of systemic vasculitis. The poor prognostic factors in CSS are renal insufficiency, cardiomyopathy, severe gastrointestinal (GI) tract, and central nervous systems (CNS) involvement. The initial management of CSS should include a high dose of a corticosteroid: prednisone at 1 mg/kg/day or its equivalent for methylprednisolone with tapering over 6 months. In patients with severe or rapidly progressing CSS, the administration of methylprednisolone pulse at 1 g/body/day for 3 days is recommended. When corticosteroid therapy does not induce remission, or when patients have poor prognostic factors, immunosuppressive cytotoxic therapy is indicated. However, some patients with severe CSS often show resistance to conventional treatment. We think that IVIG therapy is a hopeful candidate for second-line treatment for CSS patients, particularly in the case of neuropathy and/or cardiomyopathy, which are resistant to conventional therapy. However, there is not much evidence supporting the effectiveness of IVIG in CSS, and the mechanisms underlying the action of IVIG remain unclear. Now we are performing clinical trials of IVIG therapy for CSS patients who are resistant to conventional treatment, through a nationwide double-blinded placebo-controlled study in Japan.

摘要

变应性肉芽肿性血管炎(CSS)的特征为存在哮喘、嗜酸性粒细胞增多以及伴有肉芽肿的小血管血管炎。它是一种独特的疾病,这是从系统性血管炎的所有分类中确定的。CSS的不良预后因素包括肾功能不全、心肌病、严重胃肠道(GI)受累和中枢神经系统(CNS)受累。CSS的初始治疗应包括大剂量皮质类固醇:泼尼松1mg/(kg·天)或其等效的甲泼尼龙,并在6个月内逐渐减量。对于严重或快速进展的CSS患者,建议给予甲泼尼龙1g/(人·天)静脉冲击治疗3天。当皮质类固醇治疗不能诱导缓解,或患者存在不良预后因素时,应进行免疫抑制细胞毒性治疗。然而,一些严重CSS患者常对传统治疗有抵抗性。我们认为静脉注射免疫球蛋白(IVIG)治疗是CSS患者二线治疗的一个有希望的选择,特别是在神经病变和/或心肌病对传统治疗有抵抗性的情况下。然而,支持IVIG在CSS中有效性的证据不多,IVIG作用的潜在机制仍不清楚。现在我们正在日本通过一项全国性的双盲安慰剂对照研究,对抵抗传统治疗的CSS患者进行IVIG治疗的临床试验。

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