Abraham Clara, Cho Judy H
Department of Medicine, Section of Gastroenterology, University of Chicago, Chicago, Illinois 60637, USA.
Inflamm Bowel Dis. 2006 Jul;12(7):641-50. doi: 10.1097/01.MIB.0000225332.83861.5f.
Polymorphisms in NOD2 (CARD15) are associated with ileal and ileocolonic Crohn's disease, increased mortality from graft-versus-host disease, and Blau syndrome. NOD2 activation by peptidoglycan components initiates various signaling pathways and CD-associated NOD2 mutations are associated with decreased activation of NF-kappaB. NOD2 may be important for both initial defenses against commensal and pathogenic bacteria and tolerance mechanisms for maintaining controlled activation of the intestinal immune system. Significant progress has been made in defining NOD2 signaling partners and pathways and functional consequences of NOD2 mutations with respect to its activation, expression, signaling, synergistic effects with Toll-like receptor signaling, and antimicrobial effects. However, NOD2 contributions to human intestinal inflammation are complex and incompletely understood. Improved understanding of NOD2-mediated pathways may lead to identification of other molecules that can also contribute to the development of Crohn's disease in humans.
NOD2(CARD15)基因多态性与回肠及回结肠型克罗恩病、移植物抗宿主病死亡率增加以及布劳综合征相关。肽聚糖成分激活NOD2可启动多种信号通路,与克罗恩病相关的NOD2突变与核因子κB激活减少有关。NOD2对于抵御共生菌和病原菌的初始防御以及维持肠道免疫系统适度激活的耐受机制可能都很重要。在确定NOD2信号传导伙伴和途径以及NOD2突变在其激活、表达、信号传导、与Toll样受体信号传导的协同效应和抗菌作用方面的功能后果方面已经取得了重大进展。然而,NOD2对人类肠道炎症的作用很复杂,尚未完全了解。对NOD2介导途径的进一步了解可能会导致发现其他也可能导致人类克罗恩病发生的分子。