UAB Research Center of Excellence in Arsenicals, Department of Dermatology, University of Alabama at Birmingham, Birmingham AL35294, USA.
Division of Pulmonary, Allergy and Critical Care Medicine, University of Alabama at Birmingham, Birmingham AL35294, USA.
Semin Cell Dev Biol. 2022 Aug;128:120-129. doi: 10.1016/j.semcdb.2022.01.006. Epub 2022 Feb 4.
Hidradenitis suppurativa (HS) is characterized by deep-seated, highly inflamed, and painful lumps/abscesses, fistulae, and sinus tracts that grow extensively deep in the dermis and are highly immunogenic in nature. In about one-third of the HS patients there is strong evidence for the role of γ-secretase mutations along with dysregulated Notch signaling. However, the contribution of dysregulated Notch signaling in HS pathogenesis in relation to hair follicle alterations and hyper-activation of the immune system remains undefined. A genome-wide association study (GWAS), proteomic data and functional investigations of identified sequence variants in HS pathology are not fully revealing. The disease initiation or progression may involve bacterial infection besides intrinsic functional defects in keratinocytes, which may be key to further exacerbate immune cell infiltration and cytokine production in and around the lesional tissue. The absence of a suitable animal model that could fully recapitulate the pathogenesis of HS is a major impediment for proper understanding the underlying mechanisms and development of effective treatments. The presence of extracellular matrix (ECM) degradation products along with dysregulation in keratinocytes and, dermal fibroblasts ultimately affect immune regulation and are various components of HS pathogenesis. Bacterial infection further exacerbates the complexity of the disease progression. While anti-TNFα therapy shows partial efficacy, treatment to cure HS is absent. Multiple clinical trials targeting various cytokines, complement C5a and ECM products are in progress. This review provides state-of-the-art information on these aspects with a focus on dysregulated keratinocyte and immune cells; and role of ECM, and Keratin functions in this regard.
化脓性汗腺炎(HS)的特征是深层、高度炎症和疼痛的肿块/脓肿、瘘管和窦道,这些肿块/脓肿、瘘管和窦道在真皮深处广泛生长,具有高度的免疫原性。大约三分之一的 HS 患者有强烈的证据表明γ-分泌酶突变与 Notch 信号通路失调有关。然而,Notch 信号通路失调在 HS 发病机制中与毛囊改变和免疫系统过度激活的关系尚不清楚。全基因组关联研究(GWAS)、HS 病理学中鉴定的蛋白质组学数据和序列变异的功能研究并不完全清楚。疾病的发生或进展除了角质形成细胞的内在功能缺陷外,还可能涉及细菌感染,这可能是进一步加剧病变组织内和周围免疫细胞浸润和细胞因子产生的关键。缺乏能够充分重现 HS 发病机制的合适动物模型是正确理解潜在机制和开发有效治疗方法的主要障碍。细胞外基质(ECM)降解产物的存在以及角质形成细胞和真皮成纤维细胞的失调最终会影响免疫调节,是 HS 发病机制的各种组成部分。细菌感染进一步加剧了疾病进展的复杂性。虽然抗 TNF-α 治疗显示出部分疗效,但治愈 HS 的治疗方法仍不存在。针对各种细胞因子、补体 C5a 和 ECM 产物的多项临床试验正在进行中。本文综述了这些方面的最新信息,重点介绍了失调的角质形成细胞和免疫细胞,以及 ECM 和角蛋白在这方面的功能。