Genetics of inflammatory bowel disease: The role of the HLA complex

被引:95
|
作者
Ahmad, Tariq
Marshall, Sara E.
Jewell, Derek
机构
[1] Univ Oxford, Radcliffe Infirm, Gibson Labs, Gastroenterol Unit, Oxford OX2 6HE, England
[2] Univ London Imperial Coll Sci Technol & Med, Wright Fleming Inst, Dept Immunol, London SW7 2AZ, England
关键词
inflammatory bowel disease; human leucocyte antigen complex; Crohn's disease; ulcerative colitis; genetics;
D O I
10.3748/wjg.v12.i23.3628
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The human leucocyte antigen (HLA) complex on chromosome 6p21.3 is the most extensively studied genetic region in Inflammatory bowel disease (IBD). Consistent evidence of linkage to IBD3 (6p21.1-23), an area which encompasses the HLA complex, has been demonstrated for both Crohn's disease and ulcerative colitis, and a number of replicated associations with disease susceptibility and phenotype have recently emerged. However, despite these efforts the HLA susceptibility gene (s) for IBD remain elusive, a consequence of strong linkage disequilibrium, extensive polymorphism and high gene density across this region. This article reviews current knowledge of the role of HLA complex genes in IBD susceptibility and phenotype, and discusses the factors currently limiting the translation of this knowledge to clinical practice. (c) 2006 The WJG Press. All rights reserved.
引用
收藏
页码:3628 / 3635
页数:8
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