Faculté de Médecine, Université de Strasbourg et Clinique Dermatologique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Curr Rheumatol Rep. 2017 Aug;19(8):46. doi: 10.1007/s11926-017-0673-5.
We focus on recent advances in diagnosis and therapeutic strategies, as well as on pathogenesis of Schnitzler syndrome.
New diagnostic criteria were established, and their external validity was assessed in a retrospective cohort study. The cytokine interleukin-1 (IL-1) plays a crucial role in the pathogenesis of the Schnitzler syndrome, and this explains the spectacular efficiency of IL-1 blocking therapies. The Schnitzler syndrome is now considered as a late-onset acquired autoinflammatory syndrome in which the cytokine IL-1 plays a crucial role. IL-1 blocking therapies are efficient on the inflammation-linked symptoms but not on the monoclonal component. Therefore, they probably don't reduce the risk of the development of lymphoproliferative disorders that remains the main prognostic issue. The link between autoinflammation and the monoclonal component needs to be further elucidated.
本文重点关注 Schnitzler 综合征的诊断和治疗策略的最新进展,以及其发病机制。
新的诊断标准已经建立,并在一项回顾性队列研究中评估了其外部有效性。细胞因子白细胞介素-1(IL-1)在 Schnitzler 综合征的发病机制中起着关键作用,这解释了 IL-1 阻断疗法的显著疗效。 Schnitzler 综合征现在被认为是一种迟发性获得性自身炎症综合征,其中细胞因子 IL-1 起着关键作用。IL-1 阻断疗法对炎症相关症状有效,但对单克隆成分无效。因此,它们可能不会降低发生淋巴增生性疾病的风险,这仍然是主要的预后问题。自身炎症与单克隆成分之间的联系需要进一步阐明。