Low Eric E, Dellon Evan S
Division of Gastroenterology and Hepatology, University of California San Diego, San Diego, California, USA.
Center for Esophageal Diseases and Swallowing, Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
Aliment Pharmacol Ther. 2024 Feb;59(3):322-340. doi: 10.1111/apt.17845. Epub 2023 Dec 22.
Eosinophilic gastrointestinal diseases (EGIDs) are chronic, immune-mediated disorders characterised clinically by gastrointestinal symptoms and histologically by a pathologic increase in eosinophil-predominant inflammation in the gastrointestinal tract, in the absence of secondary causes of eosinophilia.
To highlight emerging insights and research efforts into the epidemiology, pathophysiology, diagnostic and therapeutic aspects of eosinophilic oesophagitis (EoE) and non-EoE EGIDs, and discuss key remaining knowledge gaps.
We selected and reviewed original research, retrospective studies, case series, randomised controlled trials, and meta-analyses.
Standardised nomenclature classifies EGIDs as EoE, eosinophilic gastritis (EoG), eosinophilic enteritis (EoN), and eosinophilic colitis (EoC). Incidence and prevalence of EoE are rising, emphasising the need to better understand how environmental risk factors and genetic features interact. Advances in understanding EoE pathophysiology have led to clinical trials of targeted therapy and the approval (in the United States) of dupilumab for EoE. Several therapies that are under investigation hope to satisfy both histologic and clinical targets. For non-EoE EGIDs, efforts are focused on better defining clinical and histopathologic disease determinants and natural history, as well as establishing new therapies.
Unmet needs for research are dramatically different for EoE and non-EoE EGIDs. In EoE, non-invasive diagnostic tests, clinicopathologic models that determine the risk of disease progression and therapeutic failure, and novel biologic therapies are emerging. In contrast, in non-EoE EGIDs, epidemiologic trends, diagnostic histopathologic thresholds, and natural history models are still developing for these more rare disorders.
嗜酸性粒细胞性胃肠疾病(EGIDs)是慢性免疫介导性疾病,临床特征为胃肠道症状,组织学特征为胃肠道中以嗜酸性粒细胞为主的炎症病理性增加,且无嗜酸性粒细胞增多的继发原因。
强调对嗜酸性粒细胞性食管炎(EoE)和非EoE型EGIDs的流行病学、病理生理学、诊断和治疗方面的新见解和研究成果,并讨论尚存的关键知识空白。
我们筛选并综述了原始研究、回顾性研究、病例系列、随机对照试验和荟萃分析。
标准化命名将EGIDs分为EoE、嗜酸性粒细胞性胃炎(EoG)、嗜酸性粒细胞性肠炎(EoN)和嗜酸性粒细胞性结肠炎(EoC)。EoE的发病率和患病率正在上升,这凸显了更好地理解环境风险因素和遗传特征如何相互作用的必要性。对EoE病理生理学认识的进展已促成靶向治疗的临床试验,并使度普利尤单抗在美国获批用于治疗EoE。几种正在研究的疗法有望实现组织学和临床目标。对于非EoE型EGIDs,研究重点在于更好地界定临床和组织病理学疾病决定因素及自然病程,以及确立新的治疗方法。
EoE和非EoE型EGIDs的未满足研究需求差异巨大。在EoE方面,非侵入性诊断测试、确定疾病进展和治疗失败风险的临床病理模型以及新型生物疗法不断涌现。相比之下,在非EoE型EGIDs中,针对这些较为罕见疾病的流行病学趋势、诊断组织病理学阈值和自然病程模型仍在发展之中。