Fanizza Jacopo, D'Amico Ferdinando, Lusetti Francesca, Fasulo Ernesto, Allocca Mariangela, Furfaro Federica, Zilli Alessandra, Parigi Tommaso Lorenzo, Radice Simona, Peyrin-Biroulet Laurent, Danese Silvio, Fiorino Gionata
Department of Gastroenterology and Endoscopy, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, 20132 Milan, Italy.
Department of Biomedical Sciences, Humanitas University, 20089 Milan, Italy.
J Clin Med. 2023 Dec 30;13(1):224. doi: 10.3390/jcm13010224.
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.
白细胞介素(IL)-23通路可促进Th17致病性反应,在炎症性肠病(IBD)的病理生理学中起关键作用。乌司奴单抗是一种靶向IL-12/23共享p40成分的单克隆抗体,具有良好的安全性,目前已被批准用于治疗对皮质类固醇和生物药物难治的IBD患者。瑞莎珠单抗、mirikizumab和古塞库单抗是用于治疗克罗恩病(CD)的特异性IL-23p19拮抗剂。然而,目前只有瑞莎珠单抗被批准用于CD治疗。目前正在进行古塞库单抗和mirikizumab的试验,初步疗效和安全性结果令人期待。在本综述中,我们总结了关于选择性IL-23抑制剂的现有知识,重点关注它们在中度至重度CD患者治疗方案中的定位。