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白细胞介素-23 抑制剂(包括 risankizumab 和 guselkumab)在棘层松解性角化不良性毛囊炎治疗中的作用。

Role of IL-23 inhibitors including risankizumab and guselkumab in the treatment of pityriasis rubra pilaris.

机构信息

Department of Dermatology, University of Rochester School of Medicine and Dentistry, 601 Elmwood Ave, Rochester, NY, USA.

Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Arch Dermatol Res. 2024 Jun 6;316(6):334. doi: 10.1007/s00403-024-03137-3.

Abstract

Pityriasis rubra pilaris (PRP) is a rare and chronic inflammatory dermatologic condition characterized by hyperkeratotic salmon-colored plaques and palmoplantar keratoderma. Traditional therapeutic modalities have shown limited efficacy and often entail potential adverse effects, highlighting the need for alternative treatment options. Our review aims to summarize the current evidence on the off-label use of IL-23 inhibitors, risankizumab and guselkumab, in the treatment of PRP. These biologic agents have been approved for psoriasis, and their potential role in managing PRP has recently garnered interest. We conducted a comprehensive literature search on PubMed and Scopus databases, identifying relevant studies published in English up to June 2023 following PRISMA guidelines. A total of 10 studies were selected for data extraction and review. Results from the selected studies demonstrated encouraging outcomes with both risankizumab and guselkumab in managing PRP. Among 11 patients treated with risankizumab, 10 showed notable improvements in various disease manifestations, including pruritus, erythema, and affected body surface area. DLQI scores and BSA percentages reported a significant improvement before and after risankizumab treatment (p = 0.0322; p = 0.0216). However, two cases also reported symptom aggravation or even disease worsening. Patients treated with guselkumab exhibited ultimate improvement in all five cases, with complete clearance in three out of five cases. DLQI and BSA percentages also reported significant improvement with treatment with guselkumab (p = 0.0172; p < 0.0001). While most cases demonstrated positive outcomes, there were isolated instances of worsening symptoms, emphasizing the need for caution and further investigation. Further research with larger sample sizes and longer follow-up periods is necessary to establish the efficacy, optimal dosing, and long-term safety of risankizumab and guselkumab in treating PRP. Overall, we provide valuable insights into the potential use of IL-23 inhibitors, risankizumab, and guselkumab, as promising treatment options for PRP. These biologics have shown efficacy in improving symptoms in treatment-resistant cases, offering new avenues for clinicians to explore in the treatment of PRP.

摘要

红糠疹(PRP)是一种罕见的慢性炎症性皮肤病,其特征为角化过度的鲑鱼色斑块和掌跖角化过度症。传统的治疗方法疗效有限,而且常常会带来潜在的不良反应,这凸显了需要替代治疗方案的必要性。我们的综述旨在总结白细胞介素 23(IL-23)抑制剂,如 risankizumab 和 guselkumab,在治疗 PRP 中的应用的现有证据。这些生物制剂已被批准用于治疗银屑病,最近它们在治疗 PRP 中的潜在作用引起了关注。我们按照 PRISMA 指南,在 PubMed 和 Scopus 数据库中进行了全面的文献检索,检索了截至 2023 年 6 月以英文发表的相关研究。共选择了 10 项研究进行数据提取和综述。从选定的研究中得出的结果表明,risankizumab 和 guselkumab 在治疗 PRP 方面都取得了令人鼓舞的效果。在接受 risankizumab 治疗的 11 名患者中,10 名患者的各种疾病表现(包括瘙痒、红斑和受累体表面积)均有显著改善。risankizumab 治疗前后的 DLQI 评分和 BSA 百分比都有显著改善(p=0.0322;p=0.0216)。然而,有两例患者也报告了症状加重甚至病情恶化。接受 guselkumab 治疗的患者在所有五例患者中均最终得到改善,其中五例中有三例完全清除。DLQI 和 BSA 百分比也显示出治疗后有显著改善(p=0.0172;p<0.0001)。虽然大多数病例的结果都是积极的,但也有孤立的症状恶化的情况,这强调了需要谨慎并进一步研究。需要进行更大样本量和更长随访时间的研究,以确定 risankizumab 和 guselkumab 治疗 PRP 的疗效、最佳剂量和长期安全性。总的来说,我们为白细胞介素 23 抑制剂、risankizumab 和 guselkumab 在治疗 PRP 方面的潜在用途提供了有价值的见解。这些生物制剂在改善治疗抵抗病例的症状方面显示出了疗效,为临床医生在治疗 PRP 方面提供了新的探索途径。

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