Markota Čagalj Adela, Marinović Branka, Bukvić Mokos Zrinka
Department of Dermatology and Venereology, University Hospital Centre Split, Spinčićeva 1, 21000 Split, Croatia.
School of Medicine, University of Split, Šoltanska 2, 21000 Split, Croatia.
Int J Mol Sci. 2022 Mar 29;23(7):3753. doi: 10.3390/ijms23073753.
Hidradenitis suppurativa (HS) is a chronic, recurrent, inflammatory skin disease deriving from the hair follicles. The formation of inflammatory nodules, abscesses, fistulas, and sinus tracts is characterized by a large inflow of key pro-inflammatory mediators, such as IFN-γ, TNF-α, IL-1, IL-17, and IL-12/23. Adalimumab is currently the only Food and Drug Administration (FDA)- and European Medicines Agency (EMA)-approved biologic therapy for moderate to severe HS in adults and adolescents. However, the long-term effectiveness of this TNF-α inhibitor in HS patients has shown to be highly variable. This review aims to review the evidence for emerging therapies that target the main pro-inflammatory cytokines in HS pathogenesis. A review of the literature was conducted, using the PubMed and Google Scholar repositories, as well as Clinicaltrials.gov. Presently, the most promising biologics in phase III trials are anti-IL-17 antibodies, secukinumab, and bimekizumab. Furthermore, an anti-IL-1 biologic, bermekimab, is currently in phase II trials, and shows encouraging results. Overall, the clinical efficacies of all new targeted therapies published up to this point are limited. More studies need to be performed to clarify the precise molecular pathology, and assess the efficacy of biological therapies for HS.
化脓性汗腺炎(HS)是一种源自毛囊的慢性、复发性炎症性皮肤病。炎症结节、脓肿、瘘管和窦道的形成特点是关键促炎介质大量流入,如干扰素-γ、肿瘤坏死因子-α、白细胞介素-1、白细胞介素-17和白细胞介素-12/23。阿达木单抗是目前唯一获得美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准用于治疗成人和青少年中重度HS的生物疗法。然而,这种肿瘤坏死因子-α抑制剂在HS患者中的长期疗效显示出高度的变异性。本综述旨在回顾针对HS发病机制中主要促炎细胞因子的新兴疗法的证据。利用PubMed、谷歌学术搜索库以及Clinicaltrials.gov进行了文献综述。目前,处于III期试验的最有前景的生物制剂是抗白细胞介素-17抗体、司库奇尤单抗和比美吉珠单抗。此外,一种抗白细胞介素-1生物制剂bermekimab目前正处于II期试验,且显示出令人鼓舞的结果。总体而言,截至目前公布的所有新靶向疗法的临床疗效都很有限。需要进行更多研究以阐明确切的分子病理学,并评估生物疗法对HS的疗效。