IRCCS Azienda Ospedaliero, Universitaria di Bologna, Via Massarenti 9, 40138 Bologna, Italy.
Department of Medical and Surgical Sciences, University of Bologna, Via Massarenti, 9, 40138 Bologna, Italy.
Int J Mol Sci. 2023 Oct 13;24(20):15165. doi: 10.3390/ijms242015165.
Eosinophilic gastrointestinal diseases (EGIDs) are an emerging group of pathological entities characterized by an eosinophil-predominant infiltration of different tracts of the gut in the absence of secondary causes of eosinophilia. According to the specific tract of the gut involved, EGIDs can be classified into eosinophilic esophagitis (EoE), eosinophilic gastritis (EoG), eosinophilic enteritis (EoN), and eosinophilic colitis (EoC). The epidemiology of EGIDs is evolving rapidly. EoE, once considered a rare disease, now has an incidence and prevalence of 7.7 new cases per 100,000 inhabitants per years and 34.4 cases per 100,000 inhabitants per year, respectively. Fewer data are available regarding non-EoE EGIDs, whose prevalence are estimated to range between 2.1 and 17.6 in 100,000 individuals, depending on age, sex, and ethnicity. Diagnosis requires the presence of suggestive symptoms, endoscopic biopsies showing abnormal values of eosinophils infiltrating the gut, and exclusion of secondary causes of eosinophilia. EoE typically presents with dysphagia and episodes of food bolus impactions, while EoG, EoN, and EoC may all present with abdominal pain and diarrhea, with or without other non-specific symptoms. In addition, although different EGIDs are currently classified as different entities, there may be overlap between different diseases in the same patient. Despite EGIDs being relatively novel pathological entities, the research on possible treatments is rapidly growing. In this regard, several randomized controlled trials are currently ongoing to investigate novel molecules, including ad-hoc steroid formulations, immunosuppressants, and mostly monoclonal antibodies that target the specific molecular mediators of EGIDs. This narrative review provides an up-to-date overview of available and investigational drugs for different EGIDs.
嗜酸细胞性胃肠道疾病(EGIDs)是一组新兴的病理实体,其特征为在没有嗜酸细胞增多的继发原因的情况下,不同肠道部位嗜酸细胞浸润为主。根据受累的具体肠道部位,EGIDs 可分为嗜酸细胞性食管炎(EoE)、嗜酸细胞性胃炎(EoG)、嗜酸细胞性肠炎(EoN)和嗜酸细胞性结肠炎(EoC)。EGIDs 的流行病学正在迅速发展。EoE 曾经被认为是一种罕见疾病,现在的发病率和患病率分别为每年每 10 万人中有 7.7 例新发病例和 34.4 例/每 10 万人,而非 EoE EGIDs 的相关数据较少,其患病率估计在每 10 万人中有 2.1 至 17.6 例,具体取决于年龄、性别和种族。诊断需要存在提示性症状、内镜活检显示肠道浸润嗜酸细胞异常值,并排除嗜酸细胞增多的继发原因。EoE 通常表现为吞咽困难和食物团块嵌塞发作,而 EoG、EoN 和 EoC 则可能都表现为腹痛和腹泻,伴有或不伴有其他非特异性症状。此外,尽管不同的 EGIDs 目前被归类为不同的实体,但同一患者可能存在不同疾病之间的重叠。尽管 EGIDs 是相对较新的病理实体,但对可能的治疗方法的研究正在迅速发展。在这方面,目前正在进行几项随机对照试验,以研究新型分子,包括专门的类固醇制剂、免疫抑制剂,以及主要针对 EGIDs 特定分子介质的单克隆抗体。本综述提供了针对不同 EGIDs 的现有和研究药物的最新概述。