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PMID: 17538633 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases.

Genes and immunity ·Vol. 8 ·No. 5 ·2007-07-00 ·Pages 387-97

De Jager PL, Franchimont D, Waliszewska A, Bitton A, Cohen A, Langelier D, Belaiche J, Vermeire S, Farwell L, Goris A, Libioulle C, Jani N, Dassopoulos T, Bromfield GP, Dubois B, Cho JH, Brant SR, Duerr RH, Yang H, Rotter JI, Silverberg MS, Steinhart AH, Daly MJ, Podolsky DK, Louis E, Hafler DA, Rioux JD, Quebec IBD Genetics Consortium, NIDDK IBD Genetics Consortium

Abstract

The intestinal flora has long been thought to play a role either in initiating or in exacerbating the inflammatory bowel diseases (IBD). Host defenses, such as those mediated by the Toll-like receptors (TLR), are critical to the host/pathogen interaction and have been implicated in IBD pathophysiology. To explore the association of genetic variation in TLR pathways with susceptibility to IBD, we performed a replication study and pooled analyses of the putative IBD risk alleles in NFKB1 and TLR4, and we performed a haplotype-based screen for association to IBD in the TLR genes and a selection of their adaptor and signaling molecules. Our genotyping of 1539 cases of IBD and pooled analysis of 4805 cases of IBD validates the published association of a TLR4 allele with risk of IBD (odds ratio (OR): 1.30, 95% confidence interval (CI): 1.15-1.48; P=0.00017) and Crohn's disease (OR: 1.33, 95% CI: 1.16-1.54; P=0.000035) but not ulcerative colitis. We also describe novel suggestive evidence that TIRAP (OR: 1.16, 95% CI: 1.04-1.30; P=0.007) has a modest effect on risk of IBD. Our analysis, therefore, offers additional evidence that the TLR4 pathway - in this case, TLR4 and its signaling molecule TIRAP - plays a role in susceptibility to IBD.

MeSH Terms
Female Gene Frequency Genetic Predisposition to Disease Genotype Haplotypes Humans Inflammatory Bowel Diseases/genetics,immunology Longitudinal Studies Male Membrane Glycoproteins/genetics,metabolism Polymorphism, Single Nucleotide Receptors, Interleukin-1/genetics,metabolism Signal Transduction Toll-Like Receptor 4/genetics,immunology,metabolism Toll-Like Receptors/genetics,metabolism
Chemicals
Membrane Glycoproteins Receptors, Interleukin-1 TIRAP protein, human TLR4 protein, human Toll-Like Receptor 4 Toll-Like Receptors
Authors & Affiliations
29 authors, click to expand affiliations / ORCID
De Jager P L
Department of Neurology, Center for Neurologic Diseases, Brigham & Women's Hospital and Harvard Medical School, Boston, MA, USA.
Franchimont D
Waliszewska A
Bitton A
Cohen A
Langelier D
Belaiche J
Vermeire S
Farwell L
Goris A
Libioulle C
Jani N
Dassopoulos T
Bromfield G P
Dubois B
Cho J H
Brant S R
Duerr R H
Yang H
Rotter J I
Silverberg M S
Steinhart A H
Daly M J
Podolsky D K
Louis E
Hafler D A
Rioux J D
Quebec IBD Genetics Consortium
NIDDK IBD Genetics Consortium
Article Info
Journal
Genes and immunity
Abbr.
Genes Immun
ISSN
1466-4879
Published
2007-07-00
Epub
2007-00-31
Pages
387-97
Language
English
Region
England
NLM ID
100953417
Subset
IM
Grants
NIDDK NIH HHS · U01 DK062420 · United States
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