Walker Marjorie M, Warwick Alasdair, Ung Chuin, Talley Nicholas J
Centre for Pathology, Faculty of Medicine, Imperial College London & Cellular Pathology, St Mary's Hospital, London W2 1NY England, UK.
Curr Gastroenterol Rep. 2011 Aug;13(4):323-30. doi: 10.1007/s11894-011-0197-5.
Functional gastrointestinal disorders (FGIDs) are common and currently defined by a symptom-based classification with no discernable pathology. In functional dyspepsia (FD), the duodenum is now implicated as a key area where symptoms originate.This is attributed to immune activation with increasing evidence indicating a role for duodenal eosinophilia. In irritable bowel syndrome (IBS), mastocytosis has been documented throughout the small and large intestine. Eosinophils and mast cells are an important link between innate and adaptive immunity, and are important in allergic type TH2 inflammation. Eosinophils may give rise to symptoms due to release of preformed cytokine proteins, which trigger neural excitation, muscle spasm, and pain. The close relationship of mast cells to nerves in IBS may similarly give rise to symptoms. Genetic studies also support of the role of innate immunity in FGIDs. The data supporting a prime role for eosinophils and mast cells in subsets of FD and IBS has become credible, and these data should be used to implement advances in diagnosis and therapeutic trials.
功能性胃肠疾病(FGIDs)很常见,目前是根据基于症状的分类来定义的,没有可识别的病理学特征。在功能性消化不良(FD)中,十二指肠现在被认为是症状起源的关键区域。这归因于免疫激活,越来越多的证据表明十二指肠嗜酸性粒细胞增多起了作用。在肠易激综合征(IBS)中,已在整个小肠和大肠中记录到肥大细胞增多。嗜酸性粒细胞和肥大细胞是固有免疫和适应性免疫之间的重要联系,在过敏性TH2型炎症中起重要作用。嗜酸性粒细胞可能由于预先形成的细胞因子蛋白的释放而引发症状,这些蛋白会触发神经兴奋、肌肉痉挛和疼痛。IBS中肥大细胞与神经的密切关系可能同样会引发症状。遗传学研究也支持固有免疫在FGIDs中的作用。支持嗜酸性粒细胞和肥大细胞在FD和IBS亚组中起主要作用的数据已变得可信,这些数据应用于推动诊断和治疗试验的进展。