Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia 30322, USA; email:
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA; email:
Annu Rev Pathol. 2021 Jan 24;16:251-275. doi: 10.1146/annurev-pathol-030320-095722. Epub 2020 Nov 24.
It is known that the gut microbiota, the numerically vast and taxonomically diverse microbial communities that thrive in a symbiotic fashion within our alimentary tract, can affect the normal physiology of the gastrointestinal tract and liver. Further, disturbances of the microbiota community structure from both endogenous and exogenous influences as well as the failure of host responsive mechanisms have been implicated in a variety of disease processes. Mechanistically, alterations in intestinal permeability and dysbiosis of the microbiota can result in inflammation, immune activation, and exposure to xenobiotic influences. Additionally, the gut and liver are continually exposed to small molecule products of the microbiota with proinflammatory, gene regulatory, and oxidative properties. Long-term coevolution has led to tolerance and incorporation of these influences into normal physiology and homeostasis; conversely, changes in this equilibrium from either the host or the microbial side can result in a wide variety of immune, inflammatory, metabolic, and neoplastic intestinal and hepatic disorders.
众所周知,肠道微生物群是在我们的消化道中以共生方式茁壮成长的数量庞大且分类多样的微生物群落,它们可以影响胃肠道和肝脏的正常生理功能。此外,肠道微生物群落结构的内外源干扰以及宿主反应机制的失效,都与多种疾病过程有关。从机制上讲,肠道通透性的改变和微生物群落的失调会导致炎症、免疫激活和接触异源影响。此外,肠道和肝脏不断受到具有促炎、基因调节和氧化特性的微生物小分子产物的影响。长期共同进化导致了对这些影响的耐受和纳入正常生理和体内平衡;相反,这种平衡无论是来自宿主还是微生物的变化,都可能导致各种免疫、炎症、代谢和肿瘤性肠道和肝脏疾病。