Department of Gastroenterology and Hepatology, Academic Medical Centre, PO Box 22660, 1100 DD, Amsterdam, The Netherlands.
Division of Gastroenterology and Hepatology, Center for Esophageal Diseases and Swallowing, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Drugs. 2019 Sep;79(13):1419-1434. doi: 10.1007/s40265-019-01173-2.
Eosinophilic esophagitis (EoE), a chronic allergic disorder of the esophagus, is characterized by symptoms of esophageal dysfunction and eosinophil-predominant inflammation. The incidence of EoE has increased substantially over the past two decades, coinciding with the so-called allergy epidemic. Current treatment options consist of dietary intervention, endoscopic dilatation, and pharmacotherapy. Given that EoE is a chronic progressive disease that is prone to relapse after cessation of therapy, these treatment options are suboptimal for long-term management. Persistent, uncontrolled esophageal inflammation is associated with esophageal remodeling and stricture formation, thus, the creation and/or discovery of alternative treatments is of paramount importance. The pathogenesis of EoE is currently under intense investigation, and recent insights concerning cellular and molecular etiology have led to the development of therapies that target specific pathophysiological pathways. This article provides an overview of established EoE pharmacotherapies, which include proton pump inhibitors and swallowed topical steroids. Additionally, anti-allergic targets, immunosuppressives, and monoclonal antibodies (such as mepolizumab, reslizumab, QAX576, RPC4046, dupilumab, omalizumab, and infliximab) that have been evaluated as treatments for EoE are summarized. Finally, several promising therapeutic agents (e.g., sialic acid-binding immunoglobulin-like lectin 8 antibodies, the transforming growth factor-β1 signal blocker losartan, CC chemokine receptor type 3 antagonists, thymic stromal lymphopoietin antibodies, antibodies targeting the α4β7 integrin, anti-interleukin-9 antibodies, and anti-interleukin-15 antibodies) that target specific molecules or cells implicated in the pathogenesis of EoE are proposed.
嗜酸粒细胞性食管炎(EoE)是一种慢性过敏性食管疾病,其特征为食管功能障碍和以嗜酸性粒细胞为主的炎症。在过去的二十年中,EoE 的发病率显著增加,与所谓的过敏流行相吻合。目前的治疗选择包括饮食干预、内镜扩张和药物治疗。鉴于 EoE 是一种慢性进行性疾病,在停止治疗后容易复发,这些治疗选择并不适合长期管理。持续、不受控制的食管炎症与食管重塑和狭窄形成有关,因此,寻找替代治疗方法至关重要。EoE 的发病机制目前正在深入研究,最近关于细胞和分子病因学的研究进展导致了针对特定病理生理途径的治疗方法的发展。本文概述了已确立的 EoE 药物治疗方法,包括质子泵抑制剂和口服局部类固醇。此外,还总结了作为 EoE 治疗方法评估的抗过敏靶点、免疫抑制剂和单克隆抗体(如美泊利珠单抗、瑞利珠单抗、QAX576、RPC4046、度普利尤单抗、奥马珠单抗和英夫利昔单抗)。最后,提出了几种有前途的治疗药物(如唾液酸结合免疫球蛋白样凝集素 8 抗体、转化生长因子-β1 信号阻滞剂洛沙坦、CC 趋化因子受体 3 拮抗剂、胸腺基质淋巴细胞生成素抗体、靶向α4β7 整合素的抗体、抗白细胞介素-9 抗体和抗白细胞介素-15 抗体),这些药物针对的是在 EoE 发病机制中涉及的特定分子或细胞。