Yan B M, Shaffer E A
Division of Gastroenterology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
Gut. 2009 May;58(5):721-32. doi: 10.1136/gut.2008.165894. Epub 2008 Dec 3.
Eosinophils are important effector cells of the innate immune system. Eosinophilic infiltrative disorders of the gastrointestinal tract, though recognised for decades, have recently witnessed a resurgence of interest, particularly for oesophageal disease. A more comprehensive basis for eosinophilic infiltration and activation has identified interleukin 5 (IL5) as a key cytokine for the differentiation and proliferation of eosinophils, while eotaxins promote the recruitment of mature eosinophils to the gut. When activated, eosinophils release multiple cytotoxic agents and immunomodulatory cytokines, resulting in local inflammation and tissue damage. Although eosinophils normally convey a defence against unwanted interlopers such as parasites, in the absence of such inciting agents, their accumulation and activation can elicit the primary infiltrative disorders of the gut: eosinophilic oesophagitis, gastroenteritis and colitis. Diagnosis of these disorders is dependent on the clinical presentation, endoscopic findings (particularly for eosinophilic oesophagitis), and most importantly, histological confirmation. Dietary modifications and topical corticosteroids are first-line treatments for eosinophilic oesophagitis. Systemic corticosteroids are the mainstay of treatment for eosinophilic gastroenteritis; surgery may be required depending on the layer of mucosa involved. Eosinophilic colitis most often occurs in infants; removal of the causative allergen usually results in a complete response. Steroids may be required for older children/adolescents or adults. This review summarises current knowledge on the trafficking of eosinophils to the gastrointestinal tract and the clinical management of the primary disorders of eosinophilic oesophagitis, eosinophilic gastroenteritis and eosinophilic colitis.
嗜酸性粒细胞是先天性免疫系统的重要效应细胞。胃肠道嗜酸性浸润性疾病虽已被认识数十年,但最近再度引起人们的关注,尤其是食管疾病。嗜酸性粒细胞浸润和激活的更全面基础已确定白细胞介素5(IL5)是嗜酸性粒细胞分化和增殖的关键细胞因子,而嗜酸性粒细胞趋化因子则促进成熟嗜酸性粒细胞向肠道募集。激活后,嗜酸性粒细胞会释放多种细胞毒性因子和免疫调节细胞因子,导致局部炎症和组织损伤。虽然嗜酸性粒细胞通常对寄生虫等外来入侵者起到防御作用,但在没有此类诱因的情况下,它们的积聚和激活会引发肠道原发性浸润性疾病:嗜酸性粒细胞性食管炎、胃肠炎和结肠炎。这些疾病的诊断取决于临床表现、内镜检查结果(特别是嗜酸性粒细胞性食管炎),最重要的是组织学确认。饮食调整和局部使用皮质类固醇是嗜酸性粒细胞性食管炎的一线治疗方法。全身使用皮质类固醇是嗜酸性粒细胞性胃肠炎的主要治疗方法;根据受累黏膜层的情况可能需要手术治疗。嗜酸性粒细胞性结肠炎最常发生于婴儿;去除致病过敏原通常会产生完全缓解。年龄较大的儿童/青少年或成人可能需要使用类固醇。本综述总结了目前关于嗜酸性粒细胞向胃肠道迁移以及嗜酸性粒细胞性食管炎、嗜酸性粒细胞性胃肠炎和嗜酸性粒细胞性结肠炎原发性疾病临床管理的知识。
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