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类天疱疮疾病的药物研发

Drug Discovery for Pemphigoid Diseases.

作者信息

Kasprick Anika, Bieber Katja, Ludwig Ralf J

机构信息

Lübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.

出版信息

Curr Protoc Pharmacol. 2019 Mar;84(1):e55. doi: 10.1002/cpph.55. Epub 2019 Feb 20.

Abstract

Pemphigoid diseases (PDs) are a group of autoimmune bullous diseases characterized and caused by autoantibodies targeting structural proteins of the skin and mucous membranes. Chronic inflammation, subepidermal blistering, and often scaring are the clinical characteristics of PDs. Itching and, in severe cases, disabilities resulting from scaring (i.e., blindness, esophageal strictures) are the leading subjective symptoms. Treatment of PDs, which is based on nonspecific immunosuppression, is challenging because of frequent relapses, lack of efficacy, and numerous adverse events. In addition, the incidence of PDs is increasing. Given the high morbidity, limited therapeutic options, and increasing incidence, there is a growing urgency for drug discovery to help treat this condition. The recent development of PD model systems has added to the understanding of PD pathogenesis and, based on these insights, new clinical trials will soon be launched. The (auto-)antibody transfer PD models allow for investigations into autoantibody-mediated tissue pathology, while immunization-induced PD models more closely resemble the clinical situation. The latter duplicate all aspects of the human disease and are useful for investigating PD pathogenesis and testing therapeutic interventions. This article describes antibody transfer and immunization-induced PD mouse models currently employed for translational PD research. © 2019 by John Wiley & Sons, Inc.

摘要

类天疱疮疾病(PDs)是一组自身免疫性大疱性疾病,其特征是由针对皮肤和粘膜结构蛋白的自身抗体引起,并由这些自身抗体导致。慢性炎症、表皮下疱形成以及常伴有瘢痕形成是PDs的临床特征。瘙痒以及在严重情况下因瘢痕形成导致的残疾(如失明、食管狭窄)是主要的主观症状。基于非特异性免疫抑制的PDs治疗具有挑战性,因为频繁复发、疗效不佳以及存在众多不良事件。此外,PDs的发病率正在上升。鉴于其高发病率、有限的治疗选择以及不断增加的发病率,药物研发以帮助治疗这种疾病的紧迫性日益增加。PD模型系统的最新发展增进了对PD发病机制的理解,基于这些见解,新的临床试验即将开展。(自身)抗体转移PD模型可用于研究自身抗体介导的组织病理学,而免疫诱导的PD模型更接近临床情况。后者复制了人类疾病的所有方面,可用于研究PD发病机制和测试治疗干预措施。本文描述了目前用于PD转化研究的抗体转移和免疫诱导的PD小鼠模型。© 2019约翰威立国际出版公司

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