Traitement des atteintes systémiques de la maladie de Sjögren

Véronique Le Guern, Gaelle Becel
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引用次数: 0

Abstract

Primary Sjögren's syndrome (SSp) is a progressive autoimmune disease characterized by a sicca syndrome but also by the occurrence of systemic manifestations. These manifestations, present in 30–40 % of patients, are varied, can involve many organs, and coexist with each other. They are of highly variable severity, and justify an adaptation of the therapeutic management which can range from a simple symptomatic treatment, to the use of immunosuppressants, biotherapies, combined therapies. The ESSDAI activity score makes it possible, in each organ system, to assess the severity and to stratify the management of these systemic disorders. Due to the wide variety of systemic damage encountered, it is important to offer multidisciplinary care. Despite active research and numerous therapeutic trials in progress or to come, no molecule has obtain agreement for the treatment of pSS. Consequently, the various therapeutic strategies that will be discussed here are essentially based on retrospective studies and expert opinions, and based and recent published recommendations.

sjogren综合征全身性疾病的治疗
原发性Sjögren's综合征(SSp)是一种进行性自身免疫性疾病,其特征为干枯综合征,但也有全身性表现。这些表现出现在30 - 40%的患者中,多种多样,可累及多个器官,并相互共存。它们的严重程度变化很大,因此有理由调整治疗管理,从简单的对症治疗到使用免疫抑制剂、生物疗法、联合疗法。ESSDAI活动评分可以在每个器官系统中评估严重程度并对这些全身性疾病的管理进行分层。由于所遇到的系统性损伤种类繁多,提供多学科治疗是很重要的。尽管积极的研究和许多正在进行或即将进行的治疗试验,但没有一种分子获得治疗pSS的协议。因此,这里讨论的各种治疗策略基本上是基于回顾性研究和专家意见,以及最近发表的建议。
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