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脓疱型银屑病及相关脓疱性皮肤病。

Pustular psoriasis and related pustular skin diseases.

机构信息

Department of Dermatology, AP-HP Hôpital Saint-Louis, 1 Avenue Claude Vellefaux, Paris CEDEX 10, 75475, France.

Sorbonne Paris Cité Université Paris Diderot, Paris, France.

出版信息

Br J Dermatol. 2018 Mar;178(3):614-618. doi: 10.1111/bjd.16232. Epub 2018 Jan 15.

Abstract

Patients with pustular psoriasis or related pustular diseases may have genetic abnormalities impairing the function of key players of the innate skin immune system. Recently, identification of these abnormalities has changed the paradigm of several of these diseases. These include generalized pustular psoriasis, palmoplantar pustular psoriasis and acrodermatitis continua of Hallopeau, and also drug-induced acute exanthematous generalized pustular eruption. Identified mutations in IL36RN, CARD14 and AP1S3 in different groups of patients lead to enhanced inflammatory cascade in several cellular subtypes including keratinocytes, and to the recruitment and activation of neutrophils and macrophages. These insights have unveiled pathophysiological features that shift the existing paradigms and emphasize the autoinflammatory nature of skin pustular disorders. They also highlight the crucial role of the innate immune system across entities belonging to the psoriasis disease spectrum, allowing identification of new appealing therapeutic targets.

摘要

患有脓疱性银屑病或相关脓疱性疾病的患者可能存在遗传异常,从而损害先天皮肤免疫系统关键成员的功能。最近,这些异常的鉴定改变了几种此类疾病的范式。其中包括泛发性脓疱性银屑病、掌跖脓疱性银屑病和 Hallopeau 连续性肢端皮炎,以及药物诱导的急性泛发性发疹性脓疱病。在不同患者群体中鉴定出的 IL36RN、CARD14 和 AP1S3 突变导致包括角质形成细胞在内的几种细胞亚型的炎症级联反应增强,并招募和激活中性粒细胞和巨噬细胞。这些发现揭示了病理生理学特征,改变了现有的范式,并强调了皮肤脓疱性疾病的自身炎症性质。它们还突出了先天免疫系统在银屑病疾病谱中不同实体中的关键作用,从而确定了新的有吸引力的治疗靶点。

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