4.6 Article

Immunogenetic biomarkers in inflammatory bowel diseases: Role of the IBD3 region

期刊

WORLD JOURNAL OF GASTROENTEROLOGY
卷 20, 期 41, 页码 15037-15048

出版社

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.3748/wjg.v20.i41.15037

关键词

IBD3; Tumor necrosis factor; MICA; HLA; Inflammatory bowel disease

资金

  1. Foundation Seneca [05748/PI/07, 04487/GERM/06]
  2. Fondo de Investigacion Sanitaria (FIS) projects CIBERehd [PI11/02644, PI11/02686]
  3. ISCII
  4. Fundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia (FFIS) [CA11/00034]

向作者/读者索取更多资源

Many studies have demonstrated the linkage between the IBD3 region (6p21.1-23), an area which encompasses the famous human leukocyte antigen (HLA) complex, and Crohn's disease (CD) or ulcerative colitis (UC). IBD3 is the only region that meets genome-wide significance, and provides stronger evidence of the linkage than 16p13.1-16q12.2 (IBD1), the locus that contains the susceptibility gene CARD15. However, despite these findings, IBD3 susceptibility genes remain elusive and unclear due to the strong linkage disequilibrium, extensive polymorphism, and high gene density that characterize this area and also due to varying allele frequencies in populations around the world. This area presents an extremely high abundance of genes, including the classical and non-classical major histocompatibility complex (MHC) class. and. genes, and other genes, namely MHC class. genes tumor necrosis factor (TNF)-alpha and -beta, and Hsp, whose proteins play key functions in immunological processes. To date, it is not clear which genes within the MHC family contribute to the IBD pathogenesis, although certain HLA alleles have been associated with IBD. Recent insights into the biological function of other genes encoded within the IBD3 region, such as the MHC class. chain-related (MIC) genes, have led investigators to a more comprehensive exploration of this region. MHC class. chain-related molecule A (MICA) is highly polymorphic and interacts with NKG2D, its receptor on the surface of NK, T-gamma delta and T CD8(+) cells. Increased expression of MICA in intestinal epithelial cells and increased expression of NKG2D in CD4(+) T cells (lamina propria) in patients with CD have also been reported. MICA alleles have also been associated with IBD, and a variation at amino acid position 129 of the alpha 2-heavy chain domain seems to categorize MICA alleles into strong and weak binders of NKG2D receptor, thereby influencing the effector cells' function. In this regard, a relevant role of MICA-129-Val/Met single nucleotide polymorphism has recently been implicated in the pathogenesis of IBD. TNF-alpha and -beta also play an important role in inflammatory response. In fact, IBD is commonly treated with TNF-alpha inhibitors. Additionally, polymorphisms of TNF-alpha gene are known to affect the gene expression level and particular TNF-alpha genotypes may influence the response of IBD patients treated with TNF-alpha inhibitors. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.

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