Vaarala Outi
Immune Response Unit, Department of Vaccination and Immune Protection, National Institute for Health and Welfare, Helsinki, Finland.
Rev Diabet Stud. 2012 Winter;9(4):251-9. doi: 10.1900/RDS.2012.9.251. Epub 2012 Dec 28.
The gut immune system has a key role in the development of autoimmune diabetes, and factors that control the gut immune system are also regulators of beta-cell autoimmunity. Gut microbiota modulate the function of the gut immune system by their effect on the innate immune system, such as the intestinal epithelial cells and dendritic cells, and on the adaptive immune system, in particular intestinal T cells. Due to the immunological link between gut and pancreas, e.g. the shared lymphocyte homing receptors, the immunological changes in the gut are reflected in the pancreas. According to animal studies, changes in gut microbiota alter the development of autoimmune diabetes. This has been demonstrated by antibiotics that induce changes in the gut microbiota. Furthermore, gut-colonizing microbes may modify the incidence of autoimmune diabetes in animal models. Deficient toll-like receptor (TLR) signaling, mediating microbial stimulus in immune cells, prevents autoimmune diabetes, which appears to be dependent on alterations in the intestinal microbiota. Although few studies have been conducted in humans, recent studies suggest that the abundance of Bacteroides and lack of butyrate-producing bacteria in fecal microbiota are associated with beta-cell autoimmunity and type 1 diabetes. It is possible that altered gut microbiota are associated with immunological aberrancies in type 1 diabetes. The changes in gut microbiota could lead to alterations in the gut immune system, such as increased gut permeability, small intestinal inflammation, and impaired tolerance to food antigens, all of which are observed in type 1 diabetes. Poor fitness of gut microbiota could explain why children who develop type 1 diabetes are prone to enterovirus infections, and do not develop tolerance to cow milk antigens. These candidate risk factors of type 1 diabetes may imply an increased risk of type 1 diabetes due to the presence of gut microbiota that do not support health. Despite the complex interaction of microbiota, host, environment, and disease mechanisms, gut microbiota are promising novel targets in the prevention of type 1 diabetes.
肠道免疫系统在自身免疫性糖尿病的发生发展中起关键作用,而控制肠道免疫系统的因素也是β细胞自身免疫的调节因子。肠道微生物群通过影响固有免疫系统(如肠道上皮细胞和树突状细胞)以及适应性免疫系统(特别是肠道T细胞)来调节肠道免疫系统的功能。由于肠道与胰腺之间存在免疫联系,例如共享淋巴细胞归巢受体,肠道的免疫变化会反映在胰腺中。根据动物研究,肠道微生物群的变化会改变自身免疫性糖尿病的发展。这已通过诱导肠道微生物群变化的抗生素得到证实。此外,肠道定植微生物可能会改变动物模型中自身免疫性糖尿病的发病率。介导免疫细胞中微生物刺激的Toll样受体(TLR)信号缺陷可预防自身免疫性糖尿病,这似乎取决于肠道微生物群的改变。尽管在人类中进行的研究较少,但最近的研究表明,粪便微生物群中拟杆菌的丰度以及产丁酸细菌的缺乏与β细胞自身免疫和1型糖尿病有关。肠道微生物群的改变可能与1型糖尿病的免疫异常有关。肠道微生物群的变化可能导致肠道免疫系统的改变,如肠道通透性增加、小肠炎症和对食物抗原的耐受性受损,所有这些在1型糖尿病中都有观察到。肠道微生物群健康状况不佳可以解释为什么患1型糖尿病的儿童容易感染肠道病毒,并且对牛奶抗原不耐受。这些1型糖尿病的候选风险因素可能意味着由于存在不利于健康的肠道微生物群,1型糖尿病的风险增加。尽管微生物群、宿主、环境和疾病机制之间存在复杂的相互作用,但肠道微生物群有望成为预防1型糖尿病的新靶点。