The Microbiome in Inflammatory Bowel Disease: Current Status and the Future Ahead

被引:1672
作者
Kostic, Aleksandar D. [1 ]
Xavier, Ramnik J. [1 ,2 ,3 ]
Gevers, Dirk [1 ]
机构
[1] Broad Inst Massachusetts Inst Technol & Harvard U, Cambridge, England
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Gastrointestinal Unit,Ctr Study Inflammatory Bowe, Boston, MA USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Computat & Integrat Biol, Boston, MA USA
基金
美国国家卫生研究院;
关键词
Microbiota; Crohn's Disease; Ulcerative Colitis; Metagenomics; MUCOSA-ASSOCIATED MICROBIOTA; CROHNS-DISEASE; FECAL MICROBIOTA; HUMAN GUT; ESCHERICHIA-COLI; ULCERATIVE-COLITIS; COLONIC MUCOSA; FAECALIBACTERIUM-PRAUSNITZII; INTESTINAL MICROBIOTA; INCREASING INCIDENCE;
D O I
10.1053/j.gastro.2014.02.009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Studies of the roles of microbial communities in the development of inflammatory bowel disease (IBD) have reached an important milestone. A decade of genome-wide association studies and other genetic analyses have linked IBD with loci that implicate an aberrant immune response to the intestinal microbiota. More recently, profiling studies of the intestinal microbiome have associated the pathogenesis of IBD with characteristic shifts in the composition of the intestinal microbiota, reinforcing the view that IBD results from altered interactions between intestinal microbes and the mucosal immune system. Enhanced technologies can increase our understanding of the interactions between the host and its resident microbiota and their respective roles in IBD from both a large-scale pathway view and at the metabolic level. We review important microbiome studies of patients with IBD and describe what we have learned about the mechanisms of intestinal microbiota dysfunction. We describe the recent progress in microbiome research from exploratory 16S-based studies, reporting associations of specific organisms with a disease, to more recent studies that have taken a more nuanced view, addressing the function of the microbiota by metagenomic and metabolomic methods. Finally, we propose study designs and methodologies for future investigations of the microbiome in patients with inflammatory gut and autoimmune diseases in general.
引用
收藏
页码:1489 / 1499
页数:11
相关论文
共 126 条
[1]
Butyrate and glucose metabolism by colonocytes in experimental colitis in mice [J].
Ahmad, MS ;
Krishnan, S ;
Ramakrishna, BS ;
Mathan, M ;
Pulimood, AB ;
Murthy, SN .
GUT, 2000, 46 (04) :493-499
[2]
Systematic review: faecal microbiota transplantation in the management of inflammatory bowel disease [J].
Anderson, J. L. ;
Edney, R. J. ;
Whelan, K. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2012, 36 (06) :503-516
[3]
Treg induction by a rationally selected mixture of Clostridia strains from the human microbiota [J].
Atarashi, Koji ;
Tanoue, Takeshi ;
Oshima, Kenshiro ;
Suda, Wataru ;
Nagano, Yuji ;
Nishikawa, Hiroyoshi ;
Fukuda, Shinji ;
Saito, Takuro ;
Narushima, Seiko ;
Hase, Koji ;
Kim, Sangwan ;
Fritz, Joelle V. ;
Wilmes, Paul ;
Ueha, Satoshi ;
Matsushima, Kouji ;
Ohno, Hiroshi ;
Olle, Bernat ;
Sakaguchi, Shimon ;
Taniguchi, Tadatsugu ;
Morita, Hidetoshi ;
Hattori, Masahira ;
Honda, Kenya .
NATURE, 2013, 500 (7461) :232-+
[4]
Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota [J].
Benjamin, Jane L. ;
Hedin, Charlotte R. H. ;
Koutsoumpas, Andreas ;
Ng, Siew C. ;
McCarthy, Neil E. ;
Prescott, Natalie J. ;
Pessoa-Lopes, Pedro ;
Mathew, Christopher G. ;
Sanderson, Jeremy ;
Hart, Ailsa L. ;
Kamm, Michael A. ;
Knight, Stella C. ;
Forbes, Alastair ;
Stagg, Andrew J. ;
Lindsay, James O. ;
Whelan, Kevin .
INFLAMMATORY BOWEL DISEASES, 2012, 18 (06) :1092-1100
[5]
ESSAY What are the consequences of the disappearing human microbiota? [J].
Blaser, Martin J. ;
Falkow, Stanley .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (12) :887-894
[6]
Translating the human microbiome [J].
Brown, James ;
de Vos, Willem M. ;
DiStefano, Peter S. ;
Dore, Joel ;
Huttenhower, Curtis ;
Knight, Rob ;
Lawley, Trevor D. ;
Raes, Jeroen ;
Turnbaugh, Peter .
NATURE BIOTECHNOLOGY, 2013, 31 (04) :304-308
[7]
Virus-Plus-Susceptibility Gene Interaction Determines Crohn's Disease Gene Atg16L1 Phenotypes in Intestine [J].
Cadwell, Ken ;
Patel, Khushbu K. ;
Maloney, Nicole S. ;
Liu, Ta-Chiang ;
Ng, Aylwin C. Y. ;
Storer, Chad E. ;
Head, Richard D. ;
Xavier, Ramnik ;
Stappenbeck, Thaddeus S. ;
Virgin, Herbert W. .
CELL, 2010, 141 (07) :1135-U64
[8]
Callaway T. R., 2008, Animal Health Research Reviews, V9, P217, DOI 10.1017/S1466252308001540
[9]
Microbiota and innate immunity in intestinal inflammation and neoplasia [J].
Cario, Elke .
CURRENT OPINION IN GASTROENTEROLOGY, 2013, 29 (01) :85-91
[10]
Casellas F, 1998, INFLAMM BOWEL DIS, V4, P1