Smith Blake, Smith Haylie, Machini Matthew
Medical School, Nova Southeastern University Dr. Kiran C. Patel College of Osteopathic Medicine, Fort Lauderdale, USA.
Medical School, Edward Via College of Osteopathic Medicine, Spartanburg, USA.
Cureus. 2024 Jul 25;16(7):e65357. doi: 10.7759/cureus.65357. eCollection 2024 Jul.
Inflammatory bowel disease (IBD) is a medical condition that causes persistent, relapsing inflammation of the gastrointestinal tract. It is an umbrella term encompassing two different conditions: ulcerative colitis (UC) and Crohn's disease (CD). The standard treatment for patients with moderate to severe CD is tumor necrosis factor-α (TNF-α) inhibitors; however, a subset of CD patients face challenges in regard to this disease's treatment. Certain populations of patients with CD may exhibit resistance or develop tolerance to TNF-α inhibitor therapy over time. The recurrent gastrointestinal inflammation associated with CD can severely impact the quality of life and lead to complications for those suffering from this condition. The symptomatic flare-ups these subpopulations continue to experience underscores why such a need for alternative therapies is desperately needed. These alternative therapies not only offer potential benefits for those with TNF-α resistance, but CD may also serve as a superior therapy option for those trying to avoid the adverse effects of CD treatments available today. This review aims to explore and investigate the novel drugs and therapies that are being investigated for the treatment of TNF-α resistant CD, such as upadacitinib, risankizumab, vedolizumab, synbiotics, fecal microbiota transplantation (FMT), and stem cell therapy. Upadacitinib is a Janus kinase inhibitor, Risankizumab is a monoclonal antibody targeting interleukin-23, and Vedolizumab is an integrin receptor antagonist. The latest advancements in CD management have shown encouraging results. Some of these novel drugs and therapies not only offer a potential solution for CD patients exhibiting resistance to TNF-α inhibitors but may also provide a superior alternative for individuals prone to opportunistic infections.
炎症性肠病(IBD)是一种导致胃肠道持续、复发炎症的病症。它是一个涵盖两种不同病症的统称:溃疡性结肠炎(UC)和克罗恩病(CD)。中重度CD患者的标准治疗方法是肿瘤坏死因子-α(TNF-α)抑制剂;然而,一部分CD患者在这种疾病的治疗上面临挑战。随着时间的推移,某些CD患者群体可能会对TNF-α抑制剂治疗产生耐药性或耐受性。与CD相关的复发性胃肠道炎症会严重影响生活质量,并给患有这种疾病的人带来并发症。这些亚群体持续经历的症状性发作凸显了对替代疗法的迫切需求。这些替代疗法不仅对那些对TNF-α耐药的患者有潜在益处,而且对于那些试图避免现有CD治疗不良反应的人来说,CD也可能是一种更好的治疗选择。本综述旨在探索和研究正在研究用于治疗TNF-α耐药性CD的新型药物和疗法,如乌帕替尼、瑞莎珠单抗、维多珠单抗、合生元、粪便微生物群移植(FMT)和干细胞疗法。乌帕替尼是一种 Janus 激酶抑制剂,瑞莎珠单抗是一种靶向白细胞介素-23的单克隆抗体,维多珠单抗是一种整合素受体拮抗剂。CD管理的最新进展已显示出令人鼓舞的结果。这些新型药物和疗法中的一些不仅为对TNF-α抑制剂表现出耐药性的CD患者提供了潜在的解决方案,而且可能为易发生机会性感染的个体提供更好的替代方案。