Clinic for Gastroenterology and Hepatology, University Clinical Center of Serbia, Belgrade, Serbia.
School of Medicine, University of Belgrade, Belgrade, Serbia.
Dig Dis. 2024;42(4):325-335. doi: 10.1159/000535647. Epub 2023 Dec 14.
Inflammatory bowel diseases (IBDs) are chronic, recurrent inflammatory diseases with partly understood etiology and pathogenesis. The course of IBD, both ulcerative colitis and Crohn's disease, is characterized by periods of relapse and remission with the possible occurrence of extraintestinal manifestations.
During the last decades, therapeutic goals in IBD evolved toward endoscopic remission and mucosal healing creating the need for early administration of disease-modifying agents (DMAs). DMAs include conventional immunosuppressants (thiopurines, methotrexate), biologic drugs (anti-TNF, anti-integrin, and anti-IL-12/23 monoclonal antibodies), and small molecules (JAK inhibitors, S1P receptor modulators). Patients with aggressive course of disease and risk factors for poor prognosis should be treated with biologic therapy early, while conventional immunomodulators should be used in those with milder course of disease in the absence of risk factors.
Challenges in the treatment of IBD patients include the choice of effective yet safe drug and prevention or overcoming loss of response.
炎症性肠病(IBD)是一种慢性、复发性炎症性疾病,其病因和发病机制尚不完全清楚。IBD 的病程,包括溃疡性结肠炎和克罗恩病,其特征是反复发作和缓解期,可能伴有肠外表现。
在过去几十年中,IBD 的治疗目标逐渐向内镜缓解和黏膜愈合发展,这就需要早期使用疾病修饰药物(DMAs)。DMAs 包括传统免疫抑制剂(硫唑嘌呤、甲氨蝶呤)、生物制剂(抗 TNF、抗整合素和抗 IL-12/23 单克隆抗体)和小分子药物(JAK 抑制剂、S1P 受体调节剂)。具有侵袭性病程和预后不良风险因素的患者应早期接受生物治疗,而对于无风险因素的轻度病程患者,应使用传统免疫调节剂。
IBD 患者的治疗挑战包括选择有效且安全的药物以及预防或克服药物应答丧失。