Jairath Vipul, Afif Waqqas, Bressler Brian, Pope Janet E, Selchen Daniel, Targownik Laura E, Panaccione Remo
Division of Gastroenterology, Western University, St. Joseph's Health Care, London, ON, Canada.
Division of Gastroenterology and Hepatology, McGill University, Montreal General Hospital, Montreal, QC H3G 1A4, Canada.
J Can Assoc Gastroenterol. 2024 May 15;7(4):282-289. doi: 10.1093/jcag/gwae013. eCollection 2024 Aug.
Ulcerative colitis (UC) is a severe and debilitating illness that affects the quality of life and physical health of many Canadians. Given the dynamic and progressive nature of the disease, advanced therapies are required to support its long-term management. The emergence of small molecule therapies offers novel treatment options that target mechanisms central to the immunopathology of UC. Sphingosine-1-phosphate (S1P) receptor modulators and Janus-activated kinase inhibitors are 2 classes of therapies that target unique pathways to attenuate inflammation and modulate the immune response characteristic of UC. This review aims to provide practical guidance on how these therapeutic options can best be used to optimize treatment management and highlight the emerging role of small molecule therapies as a treatment strategy for UC.
溃疡性结肠炎(UC)是一种严重且使人衰弱的疾病,影响着许多加拿大人的生活质量和身体健康。鉴于该疾病具有动态性和渐进性,需要先进的疗法来支持其长期管理。小分子疗法的出现提供了新的治疗选择,这些疗法针对溃疡性结肠炎免疫病理学的核心机制。鞘氨醇-1-磷酸(S1P)受体调节剂和Janus激活激酶抑制剂是两类针对独特途径以减轻炎症和调节溃疡性结肠炎特征性免疫反应的疗法。本综述旨在就如何最佳利用这些治疗选择来优化治疗管理提供实用指导,并强调小分子疗法作为溃疡性结肠炎治疗策略的新兴作用。