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原发性干燥综合征:病理生理学、临床和治疗进展。

Primary Sjögren's syndrome: pathophysiological, clinical and therapeutic advances.

机构信息

Service de rhumatologie, centre national de référence pour les maladies auto-immunes systémiques rares, hôpitaux universitaires de Strasbourg, 1, avenue Molière, 67000 Strasbourg, France.

出版信息

Joint Bone Spine. 2009 Dec;76(6):591-4. doi: 10.1016/j.jbspin.2009.09.006.

Abstract

Primary Sjögren's syndrome was long a vexing dilemma, as the underlying pathophysiological mechanisms remained obscure, disease activity was challenging to evaluate, and no specific treatments were known to be effective. However, recent years have witnessed major advances in these three areas. Convincing evidence has been obtained that innate immunity, most notably mediated by the interferons, plays a role in the initial B-cell activation. A disease activity score was developed during a consensus conference sponsored by the EULAR. Even more importantly, B-cell depletion constitutes a highly promising therapeutic approach. Thus, rituximab was effective in two controlled clinical trials.

摘要

原发性干燥综合征长期以来一直是一个令人困扰的难题,因为其潜在的病理生理机制尚不清楚,疾病活动难以评估,也没有已知的有效治疗方法。然而,近年来这三个方面都取得了重大进展。有令人信服的证据表明,先天免疫,特别是干扰素介导的先天免疫,在初始 B 细胞激活中发挥作用。在 EULAR 赞助的共识会议上制定了疾病活动评分。更重要的是,B 细胞耗竭构成了一种极具前景的治疗方法。因此,利妥昔单抗在两项对照临床试验中是有效的。

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