Garcovich Simone, De Simone Clara, Genovese Giovanni, Berti Emilio, Cugno Massimo, Marzano Angelo Valerio
Institute of Dermatology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
UOC Dermatologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Front Pharmacol. 2019 Mar 26;10:282. doi: 10.3389/fphar.2019.00282. eCollection 2019.
Targeted immune-modulating treatment with biological agents has revolutionized the management of immune-mediated inflammatory diseases, including rheumatologic conditions. The efficacy and tolerability of biological agents, from the initial tumour necrosis factor (TNF)-α inhibitors to the new anti-cytokine monoclonal antibodies, have dramatically changed the natural history of debilitating conditions such as rheumatoid arthritis and seronegative spondyloarthropathies. The widening use of biologics across several rheumatologic diseases has been associated with a new class of adverse events, the so-called paradoxical reactions. These events are inflammatory immune-mediated tissue reactions, developing paradoxically during treatment of rheumatologic conditions with targeted biologics that are commonly used for treating the idiopathic counterparts of these drug-induced reactions. The skin is frequently involved, and, even if considered rare to uncommon, these cutaneous manifestations are an important cause of biologic agent discontinuation. TNF-α antagonist-induced psoriasis, which can manifest or as exacerbation of a pre-existing form, is the prototypic and most frequent paradoxical skin reaction to biologics while other reactions, such as eczematous and lichenoid eruptions, hidradenitis suppurativa, pyoderma gangrenosum, Sweet's syndrome and granulomatous skin diseases, occur much more rarely. Management of these reactions consists of topical or systemic skin-directed therapies, depending on the severity and extension of the cutaneous picture, and it is generally associated with switching over to other disease-modifying regimens for treating the underlying rheumatologic condition. Here, we review in detail the current concepts and controversies on classification, pathogenesis and clinical management of this new class of cutaneous adverse events induced by biologics in rheumatologic patients.
使用生物制剂进行靶向免疫调节治疗彻底改变了免疫介导的炎症性疾病的管理方式,包括风湿性疾病。从最初的肿瘤坏死因子(TNF)-α抑制剂到新型抗细胞因子单克隆抗体,生物制剂的疗效和耐受性显著改变了类风湿关节炎和血清阴性脊柱关节病等使人衰弱疾病的自然病程。生物制剂在多种风湿性疾病中的广泛应用与一类新的不良事件相关,即所谓的矛盾反应。这些事件是炎症性免疫介导的组织反应,在用通常用于治疗这些药物诱导反应的特发性对应疾病的靶向生物制剂治疗风湿性疾病期间反常地发生。皮肤经常受累,即使被认为罕见至不常见,这些皮肤表现也是导致停用生物制剂的重要原因。TNF-α拮抗剂诱导的银屑病,可表现为新发或原有形式的加重,是对生物制剂最典型和最常见的矛盾皮肤反应,而其他反应,如湿疹样和苔藓样皮疹、化脓性汗腺炎、坏疽性脓皮病、Sweet综合征和肉芽肿性皮肤病,则更为罕见。这些反应的管理包括根据皮肤情况的严重程度和范围进行局部或全身性皮肤定向治疗,并且通常伴随着转而采用其他改善病情的方案来治疗潜在的风湿性疾病。在此,我们详细综述了关于风湿性疾病患者中由生物制剂引起的这类新的皮肤不良事件的分类、发病机制和临床管理的当前概念和争议。