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抗白细胞介素-23 制剂治疗银屑病的不良反应:系统评价。

Adverse Effects of Anti-Interleukin-23 Agents Employed in Patients with Psoriasis: A Systematic Review.

机构信息

Department of Dermatology, Saudi German Hospital, and Clinic, Opposite Burj Al Arab, Dubai, United Arab Emirates.

出版信息

Dermatology. 2022;238(5):886-896. doi: 10.1159/000524199. Epub 2022 Jun 13.

Abstract

BACKGROUND

Psoriasis is an immune-mediated protracted ailment that perturbs about 100 million people globally. Anti-interleukin (IL)-23 agents have a distinctive status of safety and clinical efficacy. Anti-IL-23 operatives have demonstrated therapeutic prominences in cases of psoriasis in preceding global research. However, arrays of adverse events have been associated with the anti-IL-23 agents in the remedies of psoriasis. This systematic review aimed to assess the adverse developments of anti-IL-23 operatives for patients with psoriasis determined in phase III trials.

METHODOLOGY

The PRISMA guidelines were wielded for this systematic review. The author systematically searched Google Scholar, PubMed, Scopus, and Cochrane databases to diagnosticate appropriate articles on adverse effects of anti-IL-23 agents in patients with psoriasis including the appropriate key terms (Medical Subject Headings).

RESULTS

A total of 18 studies were encompassed in this cutting-edge systematic review that met the selection criteria. In this review, the most prevailing adverse effect caused by anti-IL-23 agents was nasopharyngitis followed by headache, upper respiratory tract infection, and back pain, which are observed during the treatment with anti-IL-23 agents. The anti-IL-23 operatives, including ustekinumab and guselkumab, were significantly involved in the grade 3 stage of adverse effects for the treatment of psoriasis, whereas the anti-IL-23 agents including briakinumab, tildrakizumab, and risankizumab were significantly involved in the grade 4 stage of adverse effects.

CONCLUSION

Targeted IL-23 therapy has expeditiously upsurged to the forefront as the importance of the IL-23 axis has been progressively identified, setting a new benchmark for psoriasis outcomes. Over the last 3 years, ustekinumab, guselkumab, tildrakizumab, and risankizumab have successively come to the market. However, these drugs caused several immunological and nonimmunological side effects, but they are customarily well-tolerated and have orderly safety vignettes.

摘要

背景

银屑病是一种免疫介导的慢性疾病,全球约有 1 亿人受其困扰。抗白细胞介素(IL)-23 药物具有独特的安全性和临床疗效。抗 IL-23 药物在以前的全球研究中对银屑病病例显示出了治疗上的突出优势。然而,在银屑病的治疗中,抗 IL-23 药物与多种不良反应相关。本系统评价旨在评估在 III 期临床试验中用于治疗银屑病的抗 IL-23 药物的不良反应。

方法

本系统评价采用 PRISMA 指南。作者系统地在 Google Scholar、PubMed、Scopus 和 Cochrane 数据库中搜索了与抗 IL-23 药物治疗银屑病患者的不良反应相关的合适文章,包括适当的关键词(医学主题词)。

结果

本前瞻性系统评价共纳入 18 项符合选择标准的研究。在本综述中,抗 IL-23 药物最常见的不良反应是鼻咽炎,其次是头痛、上呼吸道感染和背痛,这些不良反应在使用抗 IL-23 药物治疗时都会出现。抗 IL-23 药物,包括乌司奴单抗和古塞库单抗,在治疗银屑病时明显涉及 3 级不良反应阶段,而抗 IL-23 药物,包括布雷卡替尼、替西珠单抗和瑞莎珠单抗,在治疗银屑病时明显涉及 4 级不良反应阶段。

结论

随着对 IL-23 轴重要性的逐步认识,靶向 IL-23 治疗迅速成为治疗银屑病的首要选择,为银屑病的治疗结果树立了新的标杆。在过去的 3 年中,乌司奴单抗、古塞库单抗、替西珠单抗和瑞莎珠单抗相继上市。然而,这些药物引起了几种免疫和非免疫相关的副作用,但通常耐受性良好,安全性良好。

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