Potestio Luca, D'Agostino Michela, Portarapillo Antonio, Esposito Valeria, Tommasino Nello, Salsano Antonia, Guerriero Luigi, Martora Fabrizio, Megna Matteo
Section of Dermatology-Department of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Napoli, Italy.
Life (Basel). 2024 Jul 24;14(8):923. doi: 10.3390/life14080923.
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.
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。