Department of Dermatology, University of Illinois at Chicago, 808 Wood St. Room 377, Chicago, IL, 60612, USA.
Department of Dermatology, Philipps University, Baldingerstr., 35043, Marburg, Germany.
Drugs. 2018 Oct;78(15):1527-1548. doi: 10.1007/s40265-018-0976-5.
Autoimmune bullous skin disorders are rare but meaningful chronic inflammatory diseases, many of which had a poor or devastating prognosis prior to the advent of immunosuppressive drugs such as systemic corticosteroids, which down-regulate the immune pathogenesis in these disorders. Glucocorticoids and adjuvant immunosuppressive drugs have been of major benefit for the fast control of most of these disorders, but their long-term use is limited by major side effects such as blood cytopenia, osteoporosis, diabetes mellitus, hypertension, and gastrointestinal ulcers. In recent years, major efforts were made to identify key elements in the pathogenesis of autoimmune bullous disorders, leading to the identification of their autoantigens, which are mainly located in desmosomes (pemphigus) and the basement membrane zone (pemphigoids). In the majority of cases, immunoglobulin G, and to a lesser extent, immunoglobulin A autoantibodies directed against distinct cutaneous adhesion molecules are directly responsible for the loss of cell-cell and cell-basement membrane adhesion, which is clinically related to the formation of blisters and/or erosions of the skin and mucous membranes. We describe and discuss novel therapeutic strategies that directly interfere with the production and regulation of pathogenic autoantibodies (rituximab), their catabolism (intravenous immunoglobulins), and their presence in the circulation and extravascular tissues such as the skin (immunoadsorption), leading to a significant amelioration of disease. Moreover, we show that these novel therapies have pleiotropic effects on various proinflammatory cells and cytokines. Recent studies in bullous pemphigoid suggest that targeting of immunoglobulin E autoantibodies (omalizumab) may be also beneficial. In summary, the introduction of targeted therapies in pemphigus and pemphigoid holds major promise because of the high efficacy and fewer side effects compared with conventional global immunosuppressive therapy.
自身免疫性大疱性皮肤病较为罕见,但却是意义重大的慢性炎症性疾病,其中许多疾病在免疫抑制药物(如全身性皮质类固醇)问世之前预后较差或具有破坏性,这些药物可下调这些疾病的免疫发病机制。糖皮质激素和辅助免疫抑制剂对大多数这些疾病的快速控制有很大的益处,但它们的长期使用受到如血液细胞减少症、骨质疏松症、糖尿病、高血压和胃肠道溃疡等主要副作用的限制。近年来,人们做出了巨大努力来确定自身免疫性大疱性疾病发病机制中的关键因素,从而确定了它们的自身抗原,这些自身抗原主要位于桥粒(天疱疮)和基底膜区(大疱性类天疱疮)。在大多数情况下,针对特定皮肤黏附分子的免疫球蛋白 G,以及在较小程度上的免疫球蛋白 A 自身抗体,直接导致细胞-细胞和细胞-基底膜黏附的丧失,这与皮肤和粘膜水疱和/或糜烂的形成在临床上相关。我们描述并讨论了直接干扰致病性自身抗体(利妥昔单抗)的产生和调节、其代谢(静脉内免疫球蛋白)以及它们在循环中和血管外组织(如皮肤)中的存在的新型治疗策略,从而导致疾病的显著改善。此外,我们还表明,这些新型疗法对各种促炎细胞和细胞因子具有多效作用。大疱性类天疱疮的最近研究表明,针对免疫球蛋白 E 自身抗体(奥马珠单抗)的靶向治疗可能也是有益的。总之,与传统的全身性免疫抑制治疗相比,靶向治疗在天疱疮和类天疱疮中的应用具有很大的前景,因为其疗效高且副作用少。