Schürmann M, Kwiatkowski R, Albrecht M, Fischer A, Hampe J, Müller-Quernheim J, Schwinger E, Schreiber S
Institute of Human Genetics, University of Lübeck, Lübeck, Germany.
Clin Exp Immunol. 2008 Jun;152(3):423-31. doi: 10.1111/j.1365-2249.2008.03621.x. Epub 2008 Apr 16.
Sarcoidosis is a multi-factorial systemic disease of granulomatous inflammation. Current concepts of the aetiology include interactions of unknown environmental triggers with an inherited susceptibility. Toll-like receptors (TLRs) are main components of innate immunity and therefore TLR genes are candidate susceptibility genes in sarcoidosis. Ten members of the human TLR gene family have been identified and mapped to seven chromosomal segments. The aim of this study was to investigate all known TLR gene loci for genetic linkage with sarcoidosis and to follow positive signals with different methods. We analysed linkage of TLR gene loci to sarcoidosis by use of closely flanking microsatellite markers in 83 families with 180 affected siblings. We found significant linkage between sarcoidosis and markers of the TLR4 gene locus on chromosome 9q (non-parametric linkage score 2.63, P = 0.0043). No linkage was found for the remaining TLR gene loci. We subsequently genotyped 1203 sarcoidosis patients from 997 families, 1084 relatives and 537 control subjects for four single nucleotide polymorphisms of TLR4, including Asp299Gly and Thr399Ile. This genotype data set was studied by case-control comparisons and transmission disequilibrium tests, but showed no significant results. In summary, TLR4 - w ith significant genetic linkage results - appears to be the most promising member of the TLR gene family for further investigation in sarcoidosis. However, our results do not confirm the TLR4 polymorphisms Asp299Gly and Thr399Ile as susceptibility markers. Our results rather point to another as yet unidentified variant within or close to TLR4 that might confer susceptibility to sarcoidosis.
结节病是一种多因素的肉芽肿性炎症全身性疾病。目前关于病因的概念包括未知环境触发因素与遗传易感性之间的相互作用。Toll样受体(TLR)是固有免疫的主要成分,因此TLR基因是结节病候选的易感基因。人类TLR基因家族的10个成员已被鉴定并定位到7个染色体区段。本研究的目的是调查所有已知的TLR基因座与结节病的遗传连锁关系,并采用不同方法追踪阳性信号。我们在83个家庭中的180名患病同胞中,使用紧密侧翼微卫星标记分析了TLR基因座与结节病的连锁关系。我们发现结节病与9号染色体上TLR4基因座的标记之间存在显著连锁(非参数连锁评分2.63,P = 0.0043)。其余TLR基因座未发现连锁关系。随后,我们对来自997个家庭的1203名结节病患者、1084名亲属和537名对照受试者进行了TLR4的4个单核苷酸多态性基因分型,包括Asp299Gly和Thr399Ile。通过病例对照比较和传递不平衡检验对该基因型数据集进行了研究,但未显示出显著结果。总之,TLR4——具有显著的遗传连锁结果——似乎是TLR基因家族中最有希望在结节病研究中进一步深入研究的成员。然而,我们的结果并未证实TLR4多态性Asp299Gly和Thr399Ile是易感标记。我们的结果反而指向TLR4内部或其附近另一个尚未确定的变异体,它可能赋予结节病易感性。