Munera-Campos M, Ballesca F, Carrascosa J M
Servicio de Dermatología, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Barcelona, España.
Servicio de Dermatología, Hospital Universitari Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Barcelona, España.
Actas Dermosifiliogr (Engl Ed). 2018 Nov;109(9):791-800. doi: 10.1016/j.ad.2018.04.003. Epub 2018 Jun 11.
Biologic drugs, which are molecules designed to act on specific immune system targets, have been shown to be very effective in treating various dermatological, rheumatological, and systemic diseases. As a group, they have an acceptable safety profile, but their use has been associated with the onset of both systemic and organ-specific inflammatory conditions. True paradoxical reactions are immune-mediated disorders that would usually respond to the biologic agent that causes them. There is still debate about whether certain other adverse reactions can be said to be paradoxical. The hypotheses proposed to explain the pathogenesis of such reactions include an imbalance in cytokine production, with an overproduction of IFN-α and altered lymphocyte recruitment and migration (mediated in part by CXCR3), and the production of autoantibodies. Some biologic therapies favor granulomatous reactions. While most of the paradoxical reactions reported have been associated with the use of TNF-α inhibitors, cases associated with more recently introduced biologic therapies -such as ustekinumab, secukinumab, and ixekizumab- are increasingly common. The study of paradoxical adverse events not only favors better management of these reactions in patients receiving biologic therapy, but also improves our knowledge of the pathogenesis of chronic inflammatory diseases and helps to identify potential therapeutic targets.
生物药物是设计用于作用于特定免疫系统靶点的分子,已被证明在治疗各种皮肤病、风湿病和全身性疾病方面非常有效。作为一个群体,它们具有可接受的安全性,但它们的使用与全身性和器官特异性炎症性疾病的发生有关。真正的矛盾反应是免疫介导的疾病,通常会对引起它们的生物制剂产生反应。关于某些其他不良反应是否可以说是矛盾的,仍存在争议。为解释此类反应的发病机制而提出的假说是细胞因子产生失衡,伴有IFN-α过度产生以及淋巴细胞募集和迁移改变(部分由CXCR3介导),以及自身抗体的产生。一些生物疗法易引发肉芽肿反应。虽然报告的大多数矛盾反应都与使用TNF-α抑制剂有关,但与最近引入的生物疗法(如乌司奴单抗、司库奇尤单抗和依奇珠单抗)相关的病例越来越常见。对矛盾不良事件的研究不仅有助于更好地管理接受生物疗法的患者的这些反应,还能增进我们对慢性炎症性疾病发病机制的了解,并有助于确定潜在的治疗靶点。