Bu Siyuan, Cheng Xiaozhen, Chen Meng, Yu Yongduo
First Clinical College, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning, People's Republic of China.
Department of Proctology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, Guangdong, People's Republic of China.
Pharmgenomics Pers Med. 2025 Sep 5;18:219-238. doi: 10.2147/PGPM.S536459. eCollection 2025.
Ulcerative colitis represents an inflammatory bowel disease with multiple contributing factors, marked by persistent inflammation of the colonic mucosa, which can lead to a reduced life expectancy and an elevated likelihood of requiring colectomy as well as developing colorectal cancer. Despite impacting roughly 5 million individuals worldwide, the intricate mechanisms underlying ulcerative colitis are still inadequately defined, hindering the development of effective treatments. Extra-intestinal complications, including enteropathic arthritis, are also addressed in the context of disease burden and management. This review explores the multifaceted pathogenesis of ulcerative colitis, emphasizing critical factors such as abnormalities in the epithelial barrier, irregular immune responses, the release of inflammatory mediators, and alterations in gut microbiota composition. We also underscore recent advancements in diagnostic biomarkers that improve the accuracy of disease detection and monitoring. Conventional medicinal strategies are reviewed alongside the emergence of biological therapies, notably those that target tumor necrosis factor (TNF), interleukins, and integrins, which have significantly altered management approaches. Established therapies (eg, 5-aminosalicylic acid, corticosteroids) and emerging agents (eg, JAK inhibitors, S1P modulators) are clearly delineated. Combination strategies-such as dual biologic regimens or JAK inhibitors combined with anti-integrin agents-are also discussed in dedicated subsections. We discuss novel therapies that utilize small molecule targeting, particularly those that inhibit Janus kinase (JAK) and modulate sphingosine-1-phosphate (S1P) receptors, presenting promising avenues for treatment. Additionally, fecal microbiota transplantation (FMT) is evaluated as a therapeutic option, as it shows promise in restoring microbial balance. Collectively, these advances underscore the pivotal roles of immune dysregulation, biologic therapies, and microbiota modulation in reshaping precision management of ulcerative colitis. This synthesis of current knowledge underscores the necessity for continued research to refine therapeutic strategies and improve patient outcomes in ulcerative colitis.
溃疡性结肠炎是一种由多种因素导致的炎症性肠病,其特征为结肠黏膜持续发炎,可导致预期寿命缩短、需要进行结肠切除术以及患结直肠癌的可能性增加。尽管全球约有500万人受到影响,但溃疡性结肠炎的复杂发病机制仍未得到充分阐明,这阻碍了有效治疗方法的开发。包括肠病性关节炎在内的肠外并发症也在疾病负担和管理的背景下进行了探讨。本综述探讨了溃疡性结肠炎的多方面发病机制,强调了上皮屏障异常、免疫反应失调、炎症介质释放以及肠道微生物群组成改变等关键因素。我们还强调了诊断生物标志物的最新进展,这些进展提高了疾病检测和监测的准确性。在回顾传统药物治疗策略的同时,还介绍了生物疗法的出现,特别是那些靶向肿瘤坏死因子(TNF)、白细胞介素和整合素的疗法,这些疗法显著改变了治疗方法。明确阐述了已有的治疗方法(如5-氨基水杨酸、皮质类固醇)和新兴药物(如JAK抑制剂、S1P调节剂)。在专门的小节中还讨论了联合策略,如双生物制剂方案或JAK抑制剂与抗整合素药物联合使用。我们讨论了利用小分子靶向的新型疗法,特别是那些抑制Janus激酶(JAK)和调节鞘氨醇-1-磷酸(S1P)受体的疗法,这些疗法为治疗提供了有前景的途径。此外,粪便微生物群移植(FMT)作为一种治疗选择也进行了评估,因为它在恢复微生物平衡方面显示出前景。总的来说,这些进展强调了免疫失调、生物疗法和微生物群调节在重塑溃疡性结肠炎精准管理中的关键作用。对当前知识的综合强调了持续研究以完善治疗策略和改善溃疡性结肠炎患者预后的必要性。