Literature DB >> 15212627

Host-bacterial interactions in inflammatory bowel disease.

Yashwant R Mahida1, Vivien E Rolfe.   

Abstract

Large numbers of different bacterial species are resident in the lumen of the distal gastrointestinal tract. The normal intestinal host-microbial interactions are not well understood, but the relationship is generally believed to be either mutually beneficial or beneficial to one without disadvantage to the other. Animal model and clinical studies suggest that IBD (inflammatory bowel disease) may develop in a susceptible individual when the normal host-bacterial relationship is dysregulated. In addition to rodent models, this article reviews studies that have investigated the cellular and molecular mechanisms of interactions between intestinal mucosal cells and the resident luminal bacteria in healthy individuals and patients with ulcerative colitis and Crohn's disease. Mechanisms by which the intestinal mucosa is able to avoid pro-inflammatory responses to commensal bacteria (and their products) but able to respond appropriately to luminal pathogens is currently an area of active investigation. Such studies are beginning to provide important clues regarding possible alterations in the mucosa that lead to the development of pro-inflammatory responses to resident bacteria in patients with IBD. Approaches to alter the intestinal microflora for therapeutic purposes and their potential mechanisms of action are also discussed.

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Year:  2004        PMID: 15212627     DOI: 10.1042/CS20040136

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  21 in total

Review 1.  Therapeutic approaches targeting intestinal microflora in inflammatory bowel disease.

Authors:  Akira Andoh; Yoshihide Fujiyama
Journal:  World J Gastroenterol       Date:  2006-07-28       Impact factor: 5.742

2.  Correlation between in vitro and in vivo immunomodulatory properties of lactic acid bacteria.

Authors:  Benoit Foligne; Sophie Nutten; Corinne Grangette; Véronique Dennin; Denise Goudercourt; Sabine Poiret; Joelle Dewulf; Dominique Brassart; Annick Mercenier; Bruno Pot
Journal:  World J Gastroenterol       Date:  2007-01-14       Impact factor: 5.742

Review 3.  The Nodosome: Nod1 and Nod2 control bacterial infections and inflammation.

Authors:  Ivan Tattoli; Leonardo H Travassos; Leticia A Carneiro; Joao G Magalhaes; Stephen E Girardin
Journal:  Semin Immunopathol       Date:  2007-08-10       Impact factor: 9.623

4.  Comparison of the fecal microbiota profiles between ulcerative colitis and Crohn's disease using terminal restriction fragment length polymorphism analysis.

Authors:  Akira Andoh; Hirotsugu Imaeda; Tomoki Aomatsu; Osamu Inatomi; Shigeki Bamba; Masaya Sasaki; Yasuharu Saito; Tomoyuki Tsujikawa; Yoshihide Fujiyama
Journal:  J Gastroenterol       Date:  2011-01-21       Impact factor: 7.527

5.  Innate immunity and inflammatory bowel disease: a review of clinical evidence and future application.

Authors:  Kyoko Katakura; Hiroshi Watanabe; Hiromasa Ohira
Journal:  Clin J Gastroenterol       Date:  2013-11-22

6.  Effects of a Lactobacillus reuteri BR11 mutant deficient in the cystine-transport system in a rat model of inflammatory bowel disease.

Authors:  Haydn L Atkins; Mark S Geier; Luca D Prisciandaro; Ashok K Pattanaik; Rebecca E A Forder; Mark S Turner; Gordon S Howarth
Journal:  Dig Dis Sci       Date:  2011-10-26       Impact factor: 3.199

7.  Culture-independent analysis of indomethacin-induced alterations in the rat gastrointestinal microbiota.

Authors:  Andrew B Dalby; Daniel N Frank; Allison L St Amand; Alison M Bendele; Norman R Pace
Journal:  Appl Environ Microbiol       Date:  2006-10       Impact factor: 4.792

8.  Adherence and cytokine induction in Caco-2 cells by bacterial populations from a three-stage continuous-culture model of the large intestine.

Authors:  Bahram Bahrami; Matthew W Child; Sandra Macfarlane; George T Macfarlane
Journal:  Appl Environ Microbiol       Date:  2011-03-04       Impact factor: 4.792

9.  Prevalence of SLC22A4 1672T and SLC22A5 -207C combination defined TC haplotype in Hungarian ulcerative colitis patients.

Authors:  Lili Magyari; Judit Bene; Katalin Komlósi; Gábor Talián; Bernadett Faragó; Veronika Csöngei; Luca Járomi; Enikô Sáfrány; Csilla Sipeky; Lilla Lakner; Márta Varga; Beáta Gasztonyi; Béla Melegh
Journal:  Pathol Oncol Res       Date:  2007-03-27       Impact factor: 3.201

10.  Cellobiose Prevents the Development of Dextran Sulfate Sodium (DSS)-Induced Experimental Colitis.

Authors:  Takashi Nishimura; Akira Andoh; Takayoshi Hashimoto; Ayako Kobori; Tomoyuki Tsujikawa; Yoshihide Fujiyama
Journal:  J Clin Biochem Nutr       Date:  2010-02-24       Impact factor: 3.114

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