González-Castro Ana M, Martínez Cristina, Salvo-Romero Eloísa, Fortea Marina, Pardo-Camacho Cristina, Pérez-Berezo Teresa, Alonso-Cotoner Carmen, Santos Javier, Vicario María
Laboratory of Neuro-Immuno-Gastroenterology, Digestive Diseases Research Unit, Vall d'Hebron Institut de Recerca, Department of Gastroenterology, Hospital Universitario Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Department of Human Molecular Genetics, Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.
J Gastroenterol Hepatol. 2017 Jan;32(1):53-63. doi: 10.1111/jgh.13417.
Irritable bowel syndrome (IBS) is one of the most prevalent gastrointestinal disorders in developed countries. Its etiology remains unknown; however, a common finding, regardless of IBS subtype, is the presence of altered intestinal barrier. In fact, signaling and location of cell-to-cell adhesion proteins, in connection with increased immune activity, seem abnormal in the intestinal epithelium of IBS patients. Despite that most research is performed on distal segments of the intestine, altered permeability has been reported in both, the small and the large bowel of all IBS subtypes. The small intestine carries out digestion and nutrient absorption and is also the site where the majority of immune responses to luminal antigens takes place. In fact, the upper intestine is more exposed to environmental antigens than the colon and is also a site of symptom generation. Recent studies have revealed small intestinal structural alterations of the epithelial barrier and mucosal immune activation in association with intestinal dysfunction, suggesting the commitment of the intestine as a whole in the pathogenesis of IBS. This review summarizes the most recent findings on mucosal barrier alterations and its relationship to symptoms arising from the small intestine in IBS, including epithelial structural abnormalities, mucosal immune activation, and microbial dysbiosis, further supporting the hypothesis of an organic origin of IBS.
肠易激综合征(IBS)是发达国家中最常见的胃肠道疾病之一。其病因尚不清楚;然而,一个共同的发现是,无论IBS的亚型如何,肠道屏障都会发生改变。事实上,在IBS患者的肠道上皮中,细胞间粘附蛋白的信号传导和定位以及免疫活性的增加似乎都不正常。尽管大多数研究是在肠道远端进行的,但所有IBS亚型的小肠和大肠都有通透性改变的报道。小肠进行消化和营养吸收,也是对腔内抗原产生大多数免疫反应的部位。事实上,上消化道比结肠更容易接触环境抗原,也是症状产生的部位。最近的研究揭示了上皮屏障的小肠结构改变和与肠道功能障碍相关的黏膜免疫激活,这表明整个肠道在IBS发病机制中起作用。这篇综述总结了关于IBS中小肠黏膜屏障改变及其与症状关系的最新发现,包括上皮结构异常、黏膜免疫激活和微生物群落失调,进一步支持了IBS有器质性起源的假说。