Clinic and Polyclinic for Dermatology and Allergology, Ludwig Maximilians University , Munich, Germany.
Derma I, München Klinik , Munich, Germany.
Expert Rev Clin Immunol. 2020 Jul;16(7):641-650. doi: 10.1080/1744666X.2020.1801420. Epub 2020 Aug 13.
Dupilumab is a treatment option newly licensed for adolescents with moderate to severe atopic dermatitis (AD). It reduces type 2 inflammation by blocking the shared receptor subunit for IL-4/-13. Dupilumab affects three disease mechanisms in atopic dermatitis: the skin barrier, the Th2-cell differentiation and the class switch to IgE. This report is based on a systematic literature search of the PubMed Database.
Dupilumab showed promising results in improving AD signs, symptoms and quality of life in adolescents with moderate to severe AD. The safety profile of dupilumab in adolescents with moderate to severe AD closely resembled the known safety profile of dupilumab in adults with moderate to severe AD. Injection-site reactions and conjunctivitis were the relevant side-effects. Skin infections were less frequently observed compared to placebo.
Dupilumab was approved by the Food and Drug Administration in March 2019 and by the European Medicines Agency in August 2019 for the treatment of adolescents with moderate to severe atopic dermatitis whose disease is not adequately controlled with topical therapies or when those therapies are not advisable. Since it is the first licensed drug it will likely become the reference drug for adolescents with moderate to severe AD.
度普利尤单抗是一种新获得许可的治疗中重度特应性皮炎(AD)的药物。它通过阻断 IL-4/-13 的共同受体亚基来减少 2 型炎症。度普利尤单抗影响特应性皮炎的三种疾病机制:皮肤屏障、Th2 细胞分化和 IgE 类别转换。本报告基于对 PubMed 数据库的系统文献检索。
度普利尤单抗在改善中重度 AD 青少年的 AD 体征、症状和生活质量方面显示出良好的效果。中重度 AD 青少年使用度普利尤单抗的安全性与中重度 AD 成人使用度普利尤单抗的已知安全性相似。相关的副作用是注射部位反应和结膜炎。与安慰剂相比,皮肤感染的发生率较低。
度普利尤单抗于 2019 年 3 月获得美国食品和药物管理局批准,2019 年 8 月获得欧洲药品管理局批准,用于治疗中重度特应性皮炎的青少年患者,这些患者的疾病经局部治疗或不建议使用这些治疗方法无法得到充分控制。由于它是第一种获得许可的药物,它可能成为中重度 AD 青少年的参考药物。