The Gut Microbiota in Inflammatory Bowel Disease

被引:81
作者
Macfarlane, G. T. [1 ]
Blackett, K. L. [1 ]
Nakayama, T. [1 ]
Steed, H. [1 ]
Macfarlane, S. [1 ]
机构
[1] Univ Dundee, Microbiol & Gut Biol Grp, Dundee DD1 9SY, Scotland
关键词
Inflammatory bowel disease; ulcerative colitis; Crohn's disease; gut microbiota; probiotics; prebiotics; synbiotics; sulphur metabolism; SULFATE-REDUCING BACTERIA; AVIUM SUBSPECIES PARATUBERCULOSIS; POLYMERASE-CHAIN-REACTION; EXPERIMENTAL ULCERATIVE-COLITIS; INVASIVE ESCHERICHIA-COLI; PLACEBO-CONTROLLED TRIAL; COLONIC CROHNS-DISEASE; HUMAN LARGE-INTESTINE; MYCOBACTERIUM-AVIUM; LACTOBACILLUS-GG;
D O I
10.2174/138161209788168146
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Crohn's disease and ulcerative colitis are the two principal forms of inflammatory bowel disease (IBD). The root causes of these chronic and acute immunological disorders are unclear, but intestinal microorganisms are known to play a key role in the initiation and maintenance of disease. However, at present, there is no clear evidence for a single transmissible agent being involved in IBD aetiology. Although marked alterations occur in faecal and mucosal bacterial communities in IBD, it is unclear whether they are responsible for causing disease, or are due to changes in the gut environment that result from inflammatory reactions and extensive tissue destruction. Despite the involvement of microorganisms in inflammatory processes, antibiotic therapy has generally been unsuccessful in IBD. However, recent studies involving the use of probiotics, prebiotics and synbiotics suggest that there is potential for controlling these diseases through manipulation of the composition of the gut microbiota, and direct interactions with the gut immune system.
引用
收藏
页码:1528 / 1536
页数:9
相关论文
共 134 条
[61]   RELATION BETWEEN CONCENTRATIONS OF METRONIDAZOLE AND BACTEROIDES SPP IN FECES OF PATIENTS WITH CROHNS-DISEASE AND HEALTHY-INDIVIDUALS [J].
KROOK, A ;
LINDSTROM, B ;
KJELLANDER, J ;
JARNEROT, G ;
BODIN, L .
JOURNAL OF CLINICAL PATHOLOGY, 1981, 34 (06) :645-650
[62]   Effect of Lactobacillus rhamnosus GG on ileal pouch inflammation and microbial flora [J].
Kuisma, J ;
Mentula, S ;
Jarvinen, H ;
Kahri, A ;
Saxelin, M ;
Farkkila, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (04) :509-515
[63]   IS901, A NEW MEMBER OF A WIDESPREAD CLASS OF ATYPICAL INSERTION SEQUENCES, IS ASSOCIATED WITH PATHOGENICITY IN MYCOBACTERIUM-AVIUM [J].
KUNZE, ZM ;
WALL, S ;
APPELBERG, R ;
SILVA, MT ;
PORTAELS, F ;
MCFADDEN, JJ .
MOLECULAR MICROBIOLOGY, 1991, 5 (09) :2265-2272
[64]  
KYLE J, 1971, GASTROENTEROLOGY, V61, P826
[65]   COURSE OF ULCERATIVE-COLITIS - ANALYSIS OF CHANGES IN DISEASE-ACTIVITY OVER YEARS [J].
LANGHOLZ, E ;
MUNKHOLM, P ;
DAVIDSEN, M ;
BINDER, V .
GASTROENTEROLOGY, 1994, 107 (01) :3-11
[66]   Clinical uniformity of inflammatory bowel disease at presentation and during the first year of disease in the north and south of Europe [J].
LennardJones, JE ;
Shivananda, S .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1997, 9 (04) :353-359
[67]   Detoxification of hydrogen sulfide and methanethiol in the cecal mucosa [J].
Levitt, MD ;
Furne, J ;
Springfield, J ;
Suarez, F ;
DeMaster, E .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (08) :1107-1114
[68]   Clinical, microbiological, and immunological effects of fructo-oligosaccharide in patients with Crohn's disease [J].
Lindsay, JO ;
Whelan, K ;
Stagg, AJ ;
Gobin, P ;
Al-Hassi, HO ;
Rayment, N ;
Kamm, MA ;
Knight, SC ;
Forbes, A .
GUT, 2006, 55 (03) :348-355
[69]   MYCOBACTERIUM-PARATUBERCULOSIS IN INTESTINAL TISSUE FROM PATIENTS WITH CROHNS-DISEASE DEMONSTRATED BY A NESTED PRIMER POLYMERASE CHAIN-REACTION [J].
LISBY, G ;
ANDERSEN, J ;
ENGBAEK, K ;
BINDER, V .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1994, 29 (10) :923-929
[70]   IMMUNOCYTOCHEMICAL EVIDENCE OF LISTERIA, ESCHERICHIA-COLI, AND STREPTOCOCCUS ANTIGENS IN CROHNS-DISEASE [J].
LIU, Y ;
VANKRUININGEN, HJ ;
WEST, AB ;
CARTUN, RW ;
CORTOT, A ;
COLOMBEL, JF .
GASTROENTEROLOGY, 1995, 108 (05) :1396-1404