医学
塞库金单抗
乌斯特基努马
伊克泽珠单抗
依那西普
阿达木单抗
银屑病
白细胞介素23
英夫利昔单抗
皮肤病科
银屑病面积及严重程度指数
白细胞介素17
肿瘤坏死因子α
内科学
免疫学
银屑病性关节炎
细胞因子
作者
Mitchel Wride,Gloria F. Chen,Sarah L. Spaulding,Elizabeth Tkachenko,Jeffrey M. Cohen
标识
DOI:10.1016/j.det.2024.02.001
摘要
Biologic therapies targeting tumor necrosis factor alpha (TNF-α) (infliximab, adalimumab, certolizumab, etanercept), the p40 subunit shared by IL-12 and IL-23 (ustekinumab), the p19 subunit of IL-23 (guselkumab, tildrakizumab, risankizumab), IL-17A (secukinumab, ixekizumab), IL-17-RA (brodalumab) and both IL-17A and IL-17F (bimekizumab) have revolutionized the treatment of psoriasis. In both the short and long term, risankizumab had highest Psoriasis Area and Severity Index 90 scores compared to other oral and injectable biologics. IL-23 inhibitors had lowest rates of short-term and long-term adverse events and most favorable long-term risk-benefit profile compared to IL-17, IL-12/23, and TNF-α inhibitors.
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