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

被引:115
作者
De Jager, P. L.
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.
机构
[1] Brigham & Womens Hosp, Ctr Neurol Dis, Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] MIT, Broad Inst, Program Med & Populat Genet, Cambridge, MA 02139 USA
[4] Harvard Univ, Cambridge, MA 02138 USA
[5] McGill Univ, Montreal Gen Hosp, Dept Internal Med, Div Gastroenterol, Montreal, PQ H3G 1A4, Canada
[6] McGill Univ, Ctr Hlth, Div Gastroenterol, Montreal, PQ H3G 1A4, Canada
[7] McGill Univ, Jewish Gen Hosp, Dept Med, Montreal, PQ H3T 1E2, Canada
[8] CHU Sherbrooke, Hop Fleurimont, Sherbrooke, PQ J1H 5N4, Canada
[9] Univ Liege, CHU, Div Gastroenterol, B-4000 Liege, Belgium
[10] Univ Hosp Gasthuisberg, Div Gastroenterol, B-3000 Louvain, Belgium
[11] Univ Louvain, Sect Expt Neurol, B-3001 Louvain, Belgium
[12] Univ Liege, Ctr Biomed Integrat Genoproteom, B-4000 Liege, Belgium
[13] Univ Pittsburgh, Sch Med, Div Gastroenterol Hepatol & Nutr, Pittsburgh, PA 15260 USA
[14] Johns Hopkins Univ, Harvey M & Lyn P Meyeroff Inflammatory Bowel Dis, Dept Med, Baltimore, MD 21218 USA
[15] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[16] Yale Univ, IBD Ctr, Dept Med, Gastroenterol Sect, New Haven, CT 06520 USA
[17] Yale Univ, IBD Ctr, Dept Genet, Gastroenterol Sect, New Haven, CT 06520 USA
[18] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21218 USA
[19] Cedars Sinai Med Ctr, Steven Spielberg Pediat Res Ctr, Dept Med, Div Med Genet, Los Angeles, CA 90048 USA
[20] Univ Toronto, Mt Sinai Hosp, IBD Ctr, Div Gastroenterol, Toronto, ON, Canada
[21] Massachusetts Gen Hosp, Ctr Study Inflammatory Bowel Dis, Dept Med, Gastrointestinal Unit, Boston, MA 02114 USA
[22] Harvard Univ, Sch Med, Boston, MA 02114 USA
[23] Univ Montreal, Montreal Heart Inst, Montreal, PQ H3C 3J7, Canada
关键词
Toll-like receptor; inflammatory bowel disease; NFKB1; TLR4; TIRAP;
D O I
10.1038/sj.gene.6364398
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:387 / 397
页数:11
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