*Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina; and †Center for Gastrointestinal Biology and Diseases, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina.
Inflamm Bowel Dis. 2014 Jan;20(1):166-75. doi: 10.1097/MIB.0b013e3182a69dca.
In the healthy gastrointestinal tract, homeostasis is an active process that requires a careful balance of host responses to the enteric luminal contents. Intestinal macrophages and dendritic cells (DCs) comprise a unique group of tissue immune cells that are ideally situated at the interface of the host and the enteric luminal environment to appropriately respond to microbes and ingested stimuli. However, intrinsic defects in macrophage and DC function contribute to the pathogenesis of inflammatory bowel diseases, as highlighted by recent genome-wide association studies. Gastrointestinal macrophages and DCs participate in inflammatory bowel disease development through inappropriate responses to enteric microbial stimuli, inefficient clearance of microbes from host tissues, and impaired transition from appropriate proinflammatory responses to anti-inflammatory responses that promote resolution. By understanding how intestinal macrophages and DCs initiate chronic inflammation, new pathogenesis-based therapeutic strategies to treat human inflammatory bowel diseases will be elucidated.
在健康的胃肠道中,稳态是一个主动的过程,需要宿主对肠腔内容物的反应进行精细的平衡。肠道巨噬细胞和树突状细胞(DC)组成了一组独特的组织免疫细胞,它们位于宿主与肠腔环境的交界处,能够对微生物和摄入的刺激物做出适当的反应。然而,巨噬细胞和 DC 功能的内在缺陷导致了炎症性肠病的发病机制,这一点最近的全基因组关联研究已经强调过了。胃肠道巨噬细胞和 DC 通过对肠内微生物刺激物的不当反应、从宿主组织中清除微生物的效率低下以及从适当的促炎反应向促进消退的抗炎反应的转变受损,参与了炎症性肠病的发展。通过了解肠道巨噬细胞和 DC 如何引发慢性炎症,将阐明针对人类炎症性肠病的基于发病机制的新治疗策略。