The interplay between microbes and the immune response in inflammatory bowel disease. (17th July 2018)

• Record Type: Journal Article
• Authors: Goethel, Ashleigh; Croitoru, Kenneth; Philpott, Dana J.
• Is Part Of: Journal of physiology. Volume 596:Number 17(2018)
• Page Start: 3869
• Page End: 3882
• Publication Date: 2018-07-17
• Subjects: inflammatory bowel diseases -- gut microbiota -- Nod2 -- NLRs -- innate immunity -- adaptive immunity -- immune‐microbe interactions; Physiology -- Periodicals; 612.005
• DOI: 10.1113/JP275396
• Languages: English
• ISSNs: 0022-3751

Abstract

Abstract: The aetiology and pathogenesis of inflammatory bowel disease (IBD) remains unclear but involves a complex interplay between genetic risk, environmental exposures, the immune system and the gut microbiota. Nearly two decades ago, the first susceptibility gene for Crohn's disease, NOD2, was identified within the IBD 1 locus. Since then, over 230 genetic risk loci have been associated with IBD and yet NOD2 remains the strongest association to date. As an intracellular innate immune sensor of bacteria, investigations into host–microbe interactions, involving both innate and adaptive immune responses, have become of particular interest in understanding the pathogenesis of IBD. Advancements in sequencing technology have lead to the groundbreaking characterization of the gut microbiota and its role in health and disease. While an altered microbiome has been described for IBD, whether it is a cause or an effect of the intestinal inflammation has yet to be determined. Moreover, the bidirectional relationship between the gut microbiota and the mucosal immune system adds to the multifaceted complexity of intestinal homeostasis. A better understanding of how host genetics, including NOD2, influence immune–microbe interactions and alter susceptibility to IBD is necessary in order to develop therapeutic and preventative treatments. Abstract : The multi‐factorial etiology of IBD. Genetically susceptible individuals may experience some form of environmental trigger that induces an immune response against gut microbiota. The uncontrolled immune activation is thought to initiate disease or result in a flare.