伊克泽珠单抗
乌斯特基努马
塞库金单抗
医学
白细胞介素23
银屑病
依那西普
阿达木单抗
白细胞介素17
英夫利昔单抗
免疫学
阿纳基纳
细胞因子
药理学
肿瘤坏死因子α
银屑病性关节炎
作者
Elisa Molinelli,Anna Campanati,Valerio Brisigotti,Annamaria Offidani
出处
期刊:Current Pharmaceutical Biotechnology
[Bentham Science]
日期:2018-03-12
卷期号:18 (12): 964-978
被引量:8
标识
DOI:10.2174/1389201019666180103140643
摘要
Background: Psoriasis is a chronic immune-mediated inflammatory skin disorder that is estimated to affect 2-3% of the general population. The IL-23/IL-17 axis is currently considered to be crucial in the pathogenesis of psoriasis. Methods: Biologics licensed for psoriasis include the TNFα inhibitors (infliximab, adalimumab, etanercept), the interleukin (IL)-12/23 monoclonal antibody (ustekinumab), and IL-17 inhibitor (secukinumab, ixekizumab). Results: In this section, we analyse the role of IL-12, IL-23, and IL-17 in psoriasis and evaluated the efficacy and safety of biologic therapies targeting this cytokine. Conclusion: Dosing regimens, administration modality, and pharmacodynamics profiles of currently available anti-IL-12/IL-23 and IL-17 inhibitors are also examined. Keywords: Ustekinumab, secukinumab, brodalumab, ixekizumab, efficacy, safety.
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