Tian Zhezhe, Zhao Qiaorui, Teng Xiu
Laboratory of Human Disease and Immunotherapies, West China Hospital, Sichuan University, Chengdu, China.
Hepatic Department of Hepatology, Qilu Hospital of Shandong University, Jinan, China.
Front Immunol. 2024 Jul 17;15:1393463. doi: 10.3389/fimmu.2024.1393463. eCollection 2024.
IBD (inflammatory bowel disease) is a chronic inflammatory disease of the gastrointestinal tract with increasing incidence worldwide. Multiple factors, such as genetic background, environmental and luminal factors, and mucosal immune dysregulation, have been implicated in the cause of IBD, although the cause of the disease remains unknown. IL-12 and IL-23 and their downstream signaling pathways participate in the pathogenesis of inflammatory bowel disease. Early and aggressive treatment with biologic therapies or novel small molecules is needed to decrease complications and the need for hospitalization and surgery. The landscape of inflammatory bowel disease (IBD) treatment has tremendously improved with the development of biologics and small molecule drugs. Several novel biologics and small molecule drugs targeting IL-12 and IL-23 and their downstream targets have shown positive efficacy and safety data in clinical trials, and several drugs have been approved for the treatment of IBD. In the future, numerous potential emerging therapeutic options for IBD treatment are believed to come to the fore, achieving disease cure.
炎症性肠病(IBD)是一种胃肠道慢性炎症性疾病,在全球范围内发病率呈上升趋势。尽管该疾病的病因尚不清楚,但多种因素,如遗传背景、环境和肠腔因素以及黏膜免疫失调,都与IBD的病因有关。白细胞介素-12(IL-12)和白细胞介素-23(IL-23)及其下游信号通路参与炎症性肠病的发病机制。需要早期积极采用生物疗法或新型小分子药物进行治疗,以减少并发症以及住院和手术需求。随着生物制剂和小分子药物的发展,炎症性肠病(IBD)的治疗前景有了极大改善。几种针对IL-12和IL-23及其下游靶点的新型生物制剂和小分子药物在临床试验中显示出了积极的疗效和安全性数据,并且有几种药物已被批准用于治疗IBD。未来,预计会有众多潜在的新兴IBD治疗选择脱颖而出,实现疾病治愈。