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1
Emerging Role of Biologic Drugs Targeting IL-17 and IL-23: Pityriasis Rubra Pilaris.靶向IL-17和IL-23的生物药物的新作用:红皮病型毛发红糠疹
Life (Basel). 2024 Jul 24;14(8):923. doi: 10.3390/life14080923.
2
Biologics for pityriasis rubra pilaris treatment: A review of the literature.生物制剂治疗毛发红糠疹:文献综述。
J Am Acad Dermatol. 2018 Aug;79(2):353-359.e11. doi: 10.1016/j.jaad.2018.03.036. Epub 2018 Mar 30.
3
Biologics for Treatment of Pityriasis Rubra Pilaris: A Literature Review.用于治疗毛发红糠疹的生物制剂:文献综述
J Cutan Med Surg. 2024 May-Jun;28(3):269-275. doi: 10.1177/12034754241238735. Epub 2024 Mar 28.
4
A Case of Meningococcal and HSV-2 Meningitis in a Patient Being Treated with Ustekinumab for Pityriasis Rubra Pilaris.一例使用乌司奴单抗治疗红皮病型毛发红糠疹的患者并发脑膜炎奈瑟菌和单纯疱疹病毒2型脑膜炎
Eur J Case Rep Intern Med. 2020 May 22;7(8):001615. doi: 10.12890/2020_001615. eCollection 2020.
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Role of IL-23 inhibitors including risankizumab and guselkumab in the treatment of pityriasis rubra pilaris.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。
Arch Dermatol Res. 2024 Jun 6;316(6):334. doi: 10.1007/s00403-024-03137-3.
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Secukinumab for the treatment of adult-onset pityriasis rubra pilaris: a single-arm clinical trial with transcriptomic analysis.司库奇尤单抗治疗成人发病性毛发红糠疹:一项带有转录组分析的单臂临床试验。
Br J Dermatol. 2022 Nov;187(5):650-658. doi: 10.1111/bjd.21708. Epub 2022 Jul 15.
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Interleukin 23-Helper T Cell 17 Axis as a Treatment Target for Pityriasis Rubra Pilaris.白细胞介素 23-辅助性 T 细胞 17 轴作为治疗毛发红糠疹的靶点。
JAMA Dermatol. 2017 Apr 1;153(4):304-308. doi: 10.1001/jamadermatol.2016.5384.
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Use of Biologics in Pityriasis Rubra Pilaris Refractory to First-Line Systemic Therapy: A Systematic Review [Formula: see text].生物制剂在一线全身治疗难治性红皮病性银屑病中的应用:系统评价[公式:见正文]。
J Cutan Med Surg. 2020 Jan/Feb;24(1):73-78. doi: 10.1177/1203475419887731. Epub 2019 Nov 6.
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Management of refractory pityriasis rubra pilaris: challenges and solutions.难治性毛发红糠疹的管理:挑战与解决方案
Clin Cosmet Investig Dermatol. 2017 Nov 9;10:451-457. doi: 10.2147/CCID.S124351. eCollection 2017.
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Refractory pityriasis rubra pilaris treated with etanercept, adalimumab, or ustekinumab: A retrospective investigation.难治性毛发红糠疹用依那西普、阿达木单抗或乌司奴单抗治疗:一项回顾性研究。
Dermatol Ther. 2017 Nov;30(6). doi: 10.1111/dth.12559. Epub 2017 Oct 15.

引用本文的文献

1
Pityriasis Rubra Pilaris Following COVID-19 Infection: A Case of Successful Treatment With Ixekizumab.新型冠状病毒肺炎感染后红皮病型毛发红糠疹:1例使用司库奇尤单抗成功治疗的病例
Cureus. 2025 Feb 7;17(2):e78668. doi: 10.7759/cureus.78668. eCollection 2025 Feb.

本文引用的文献

1
Tildrakizumab use for recalcitrant pityriasis rubra pilaris.替拉珠单抗用于治疗顽固性毛发红糠疹。
Australas J Dermatol. 2024 Aug;65(5):476-479. doi: 10.1111/ajd.14307. Epub 2024 May 30.
2
Risankizumab for the treatment of pityriasis rubra pilaris postanaplastic large cell lymphoma.司库奇尤单抗用于治疗间变性大细胞淋巴瘤后的红皮病型毛发红糠疹。
JAAD Case Rep. 2024 Apr 23;48:108-111. doi: 10.1016/j.jdcr.2024.03.023. eCollection 2024 Jun.
3
Pityriasis rubra pilaris after COVID-19 vaccination: successful treatment with ustekinumab.新冠病毒疫苗接种后出现的红皮病型毛发红糠疹:使用乌司奴单抗成功治疗
An Bras Dermatol. 2024 Jul-Aug;99(4):642-644. doi: 10.1016/j.abd.2023.07.009. Epub 2024 Apr 22.
4
Guselkumab for Pityriasis Rubra Pilaris and Dysregulation of IL-23/IL-17 and NFkB Signaling: A Nonrandomized Trial.古塞单抗治疗红皮病性银屑病和 IL-23/IL-17 和 NFkB 信号通路失调:一项非随机试验。
JAMA Dermatol. 2024 Jun 1;160(6):641-645. doi: 10.1001/jamadermatol.2024.0257.
5
Biologics for Treatment of Pityriasis Rubra Pilaris: A Literature Review.用于治疗毛发红糠疹的生物制剂:文献综述
J Cutan Med Surg. 2024 May-Jun;28(3):269-275. doi: 10.1177/12034754241238735. Epub 2024 Mar 28.
6
Updates on Pityriasis Rubra Pilaris: A Scoping Review.关于红癣:范围综述的最新进展。
J Cutan Med Surg. 2024 Mar-Apr;28(2):158-166. doi: 10.1177/12034754231223159. Epub 2024 Jan 4.
7
Pityriasis Rubra Pilaris: An Updated Review of Clinical Presentation, Etiopathogenesis, and Treatment Options.红癣:临床特征、发病机制及治疗选择的最新综述。
Am J Clin Dermatol. 2024 Mar;25(2):243-259. doi: 10.1007/s40257-023-00836-x. Epub 2023 Dec 30.
8
Bimekizumab in refractory pityriasis rubra pilaris.比美吉珠单抗治疗难治性毛发红糠疹
J Dtsch Dermatol Ges. 2024 Jan;22(1):102-104. doi: 10.1111/ddg.15252. Epub 2023 Dec 8.
9
Erythrodermic pityriasis rubra pilaris following SARS-CoV-2 vaccination treated with bimekizumab.用比美吉珠单抗治疗的新型冠状病毒2型疫苗接种后发生的红皮病型毛发红糠疹
JAAD Case Rep. 2023 Oct 4;42:7-11. doi: 10.1016/j.jdcr.2023.09.024. eCollection 2023 Dec.
10
Exploring Psoriasis Inflammatory Microenvironment by NanoString Technologies.利用纳米串技术探索银屑病炎症微环境
J Clin Med. 2023 Oct 28;12(21):6820. doi: 10.3390/jcm12216820.

靶向IL-17和IL-23的生物药物的新作用:红皮病型毛发红糠疹

Emerging Role of Biologic Drugs Targeting IL-17 and IL-23: Pityriasis Rubra Pilaris.

作者信息

Potestio Luca, D'Agostino Michela, Portarapillo Antonio, Esposito Valeria, Tommasino Nello, Salsano Antonia, Guerriero Luigi, Martora Fabrizio, Megna Matteo

机构信息

Section of Dermatology-Department of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Napoli, Italy.

出版信息

Life (Basel). 2024 Jul 24;14(8):923. doi: 10.3390/life14080923.

DOI:10.3390/life14080923
PMID:39202665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11355122/
Abstract

Pityriasis rubra pilaris (PRP) is a rare, papulosquamous, inflammatory skin disease. PRP represents a therapeutic challenge. The rarity of this disease and its possible spontaneous remission makes the conduction and interpretation of therapeutic studies particularly difficult. Moreover, PRP not infrequently proves resistant to common topical and conventional systemic therapies. In this context, numerous biologic agents have been reported in PRP treatment. The aim of our manuscript was to review the current literature to evaluate the possible role of biologics targeting the IL17/23 axis in PRP management. Recent cases in the literature have highlighted the use of several promising drugs: IL-17 inhibitors, IL-23 inhibitors, and the IL-12/23p40 inhibitor ustekinumab. However, it should be noted that all these drugs are approved for moderate-to-severe plaque psoriasis and their use in PRP is off label. The treatment of PRP is based on clinical experience, case reports or case series reported in the literature, as randomized controlled trials are difficult to conduct due to the rarity of the condition. Despite data on the efficacy of drugs targeting IL-17 and IL-23 being promising, they are still limited. Certainly, further studies are desirable to better characterize PRP and establish shared guidelines.

摘要

红皮病型毛发红糠疹(PRP)是一种罕见的丘疹鳞屑性炎症性皮肤病。PRP是一个治疗难题。这种疾病的罕见性及其可能的自发缓解使得治疗研究的开展和解读尤为困难。此外,PRP常常对常用的局部治疗和传统的全身治疗耐药。在此背景下,已有多种生物制剂被报道用于PRP治疗。我们撰写本文的目的是回顾当前文献,以评估靶向IL17/23轴的生物制剂在PRP治疗中的可能作用。文献中的近期病例突出了几种有前景药物的使用:IL-17抑制剂、IL-23抑制剂以及IL-12/23p40抑制剂乌司奴单抗。然而,应当注意的是,所有这些药物均被批准用于中重度斑块状银屑病,它们在PRP中的使用属于超适应症用药。PRP的治疗基于临床经验、文献报道的病例报告或病例系列,因为由于该病的罕见性,很难进行随机对照试验。尽管靶向IL-17和IL-23的药物疗效数据很有前景,但仍然有限。当然,需要进一步研究以更好地描述PRP并制定共同的指南。