杜皮鲁玛
特应性皮炎
医学
湿疹面积及严重程度指数
免疫学
白细胞介素23
单克隆抗体
细胞因子
皮肤病科
白细胞介素
抗体
作者
Jennifer D. Hamilton,Benjamin Ungar,Emma Guttman‐Yassky
出处
期刊:Immunotherapy
[Future Medicine]
日期:2015-10-01
卷期号:7 (10): 1043-1058
被引量:84
摘要
Atopic dermatitis (AD) is characterized by type 2 helper T (Th2) cell-driven inflammation. Dupilumab is a fully human monoclonal antibody directed against the IL-4 receptor α subunit that blocks the signaling of IL-4 and IL-13, both key cytokines in Th2-mediated pathways. In Phase I and II studies of adults with moderate-to-severe AD, dupilumab administered as monotherapy or with topical corticosteroids resulted in rapid, significant improvements in clinical efficacy, patient-reported outcomes, and Th2-related serum and tissue biomarkers, and shifted the RNA expression profile of lesional skin to a more nonlesional signature. In all clinical studies to date, dupilumab has shown a favorable safety profile with no dose-limiting toxicity. The robust effects of dupilumab on skin inflammation and pruritus confirm the pathogenic role of IL-4 and IL-13 signaling in adult AD, and further support the application of Th2 cytokine antagonists in the treatment of this disease.
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