Division of Gastroenterology, Center for Autoimmune Liver Diseases, European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, 20125 Milan, Italy.
Cells. 2023 Oct 18;12(20):2473. doi: 10.3390/cells12202473.
Eosinophilic esophagitis (EoE) is a chronic inflammatory disease characterized by eosinophilic infiltration of the esophagus. It arises from a complex interplay of genetic predisposition (susceptibility loci), environmental triggers (allergens and dietary antigens), and a dysregulated immune response, mainly mediated by type 2 T helper cell (Th2)-released cytokines, such as interleukin (IL)-4, IL-5, and IL-13. These cytokines control eosinophil recruitment and activation as well as tissue remodeling, contributing to the characteristic features of EoE. The pathogenesis of EoE includes epithelial barrier dysfunction, mast cell activation, eosinophil degranulation, and fibrosis. Epithelial barrier dysfunction allows allergen penetration and promotes immune cell infiltration, thereby perpetuating the inflammatory response. Mast cells release proinflammatory mediators and promote eosinophil recruitment and the release of cytotoxic proteins and cytokines, causing tissue damage and remodeling. Prolonged inflammation can lead to fibrosis, resulting in long-term complications such as strictures and dysmotility. Current treatment options for EoE are limited and mainly focus on dietary changes, proton-pump inhibitors, and topical corticosteroids. Novel therapies targeting key inflammatory pathways, such as monoclonal antibodies against IL-4, IL-5, and IL-13, are emerging in clinical trials. A deeper understanding of the complex pathogenetic mechanisms behind EoE will contribute to the development of more effective and personalized therapeutic strategies.
嗜酸性食管炎(EoE)是一种慢性炎症性疾病,其特征是食管嗜酸性粒细胞浸润。它源于遗传易感性(易感基因座)、环境触发因素(过敏原和饮食抗原)和免疫反应失调之间的复杂相互作用,主要由 2 型辅助性 T 细胞(Th2)释放的细胞因子介导,如白细胞介素(IL)-4、IL-5 和 IL-13。这些细胞因子控制嗜酸性粒细胞募集和激活以及组织重塑,有助于 EoE 的特征表现。EoE 的发病机制包括上皮屏障功能障碍、肥大细胞激活、嗜酸性粒细胞脱颗粒和纤维化。上皮屏障功能障碍允许过敏原穿透并促进免疫细胞浸润,从而使炎症反应持续存在。肥大细胞释放促炎介质,促进嗜酸性粒细胞募集和细胞毒性蛋白和细胞因子的释放,导致组织损伤和重塑。长期炎症可导致纤维化,导致长期并发症,如狭窄和运动障碍。目前 EoE 的治疗选择有限,主要集中在饮食改变、质子泵抑制剂和局部皮质类固醇上。针对关键炎症途径的新型治疗方法,如针对 IL-4、IL-5 和 IL-13 的单克隆抗体,正在临床试验中出现。对 EoE 背后复杂发病机制的更深入了解将有助于开发更有效和个性化的治疗策略。