Breban Maxime, Miceli-Richard Corinne, Zinovieva Elena, Monnet Dominique, Said-Nahal Roula
Département d'immunologie, institut Cochin, Inserm U567/CNRS UMR8104/IFR116, hôpital Cochin, 27, rue du Faubourg-Saint-Jacques, 75014 Paris, France.
Joint Bone Spine. 2006 Jul;73(4):355-62. doi: 10.1016/j.jbspin.2005.11.010. Epub 2006 Mar 20.
The spondyloarthropathies constitute a group of inflammatory joint diseases linked by shared characteristics that include a strong common genetic background. Genetic factors include major histocompatibility complex (MHC) genes, among which HLA-B27 contributes 30% of the overall genetic susceptibility to spondyloarthropathies, and non-MHC genes, none of which have been identified to date. Genome screens have identified regions that may contain susceptibility genes for spondyloarthropathies. In particular, a locus on the long arm of chromosome 9 (9q31-34) was identified by two groups working independently from each other. Studies using the candidate gene approach ruled out a role for most of the tested genes, including CARD15/NOD2. However, several independent groups have reported significant associations between ankylosing spondylitis and the IL-1 gene cluster on the long arm of chromosome 2.
脊柱关节病是一组具有共同特征的炎性关节疾病,这些特征包括强大的共同遗传背景。遗传因素包括主要组织相容性复合体(MHC)基因,其中HLA - B27占脊柱关节病总体遗传易感性的30%,以及非MHC基因,迄今为止尚未确定其中任何一种基因。全基因组筛查已经确定了可能包含脊柱关节病易感基因的区域。特别是,9号染色体长臂(9q31 - 34)上的一个位点被两个彼此独立工作的小组所确定。使用候选基因方法的研究排除了大多数测试基因的作用,包括CARD15/NOD2。然而,几个独立的小组报告了强直性脊柱炎与2号染色体长臂上的IL - 1基因簇之间存在显著关联。