医学
乌斯特基努马
克罗恩病
白细胞介素23
炎症性肠病
单克隆抗体
单克隆
耐火材料(行星科学)
银屑病
疾病
伊克泽珠单抗
免疫学
塞库金单抗
内科学
白细胞介素
抗体
细胞因子
阿达木单抗
物理
银屑病性关节炎
天体生物学
作者
Jacopo Fanizza,Ferdinando D’Amico,Francesca Lusetti,Ernesto Fasulo,Mariangela Allocca,Federica Furfaro,Alessandra Zilli,Tommaso Lorenzo Parigi,Simona Radice,Laurent Peyrin‐Biroulet,Silvio Danese,Gionata Fiorino
摘要
Promoting a Th17 pathogenic response, the interleukin (IL)-23 pathway is crucial in the pathophysiology of inflammatory bowel disease (IBD). With a favorable safety profile, ustekinumab, a monoclonal antibody targeting the shared p40 component of IL-12/23, is currently approved for the treatment of IBD in patients with disease refractory to corticosteroids and biologic drugs. Risankizumab, mirikizumab, and guselkumab are specific IL-23p19 antagonists tested for the treatment of Crohn’s disease (CD). However, only risankizumab currently has been approved for its treatment. Trials with guselkumab and mirikizumab are currently ongoing, with promising preliminary efficacy and safety results. In this review, we provide a summary of the current knowledge about selective IL-23 inhibitors, focusing on their positioning in the therapeutic algorithm of patients with moderate to severe CD.
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