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使用生物制剂和小分子抑制剂治疗黑利-黑利病:一项系统评价。

Treatment of Hailey-Hailey disease with biologics and small-molecule inhibitors: a systematic review.

作者信息

Liu Wei, Xue Xiao, Li Shanshan

机构信息

Department of Dermatology and Venereology, First Hospital of Jilin University, Changchun, China.

Department of Laboratory Medicine, First Hospital of Jilin University, Changchun, China.

出版信息

Clin Exp Dermatol. 2024 Dec 23;50(1):38-45. doi: 10.1093/ced/llae298.

Abstract

Hailey-Hailey disease (HHD) is a rare genetic dermatosis characterized by recurrent flaccid vesicles and blisters on erythematous skin in friction areas. The disease follows a chronic relapsing course and has a significant psychological and social impact. Currently, there is no standardized therapeutic regimen for HHD, posing a challenge for dermatologists in managing the condition. We performed this systematic review to investigate the therapeutic role of biologics and small-molecule inhibitors in the treatment of HHD. A systematic search was conducted of the PubMed, Embase, Web of Science, Scopus and Cochrane databases from inception to 1 January 2024. In total, 31 patients with HHD from 18 articles were included in the analysis. Biologics and small-molecule inhibitors were evaluated, including dupilumab, apremilast, upadacitinib, abrocitinib, adalimumab and etanercept. Most reported cases demonstrated clinical improvement after treatment initiation, with few major adverse events. However, some patients experienced recurrences. In conclusion, biologics and small-molecule inhibitors may offer a treatment alternative for patients with refractory HHD, but further confirmation is necessary through large-scale randomized controlled clinical trials.

摘要

黑利-黑利病(HHD)是一种罕见的遗传性皮肤病,其特征为摩擦部位的红斑皮肤上反复出现松弛性水疱和大疱。该病呈慢性复发性病程,对心理和社会有重大影响。目前,HHD尚无标准化的治疗方案,这给皮肤科医生治疗该病带来了挑战。我们进行了这项系统评价,以研究生物制剂和小分子抑制剂在HHD治疗中的作用。对PubMed、Embase、Web of Science、Scopus和Cochrane数据库从创建至2024年1月1日进行了系统检索。分析共纳入了18篇文章中的31例HHD患者。对生物制剂和小分子抑制剂进行了评估,包括度普利尤单抗、阿普米拉斯、乌帕替尼、阿布罗替尼、阿达木单抗和依那西普。大多数报告的病例在开始治疗后显示出临床改善,且很少有严重不良事件。然而,一些患者出现了复发。总之,生物制剂和小分子抑制剂可能为难治性HHD患者提供一种治疗选择,但需要通过大规模随机对照临床试验进一步证实。

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