Thomson G, Nicholas F W, Bodmer W F, O'Neill M E, Hedrick P W, Hudes E
Tissue Antigens. 1985 Nov;26(5):293-306. doi: 10.1111/j.1399-0039.1985.tb02227.x.
The nature and extent of negative and multiple HLA antigen disease associations are investigated theoretically under two models. The first model assumes that an HLA antigen is involved directly in predisposing individuals to disease. The second model assumes that the association of a particular HLA antigen(s) with a disease is the result of linkage disequilibrium between the allele determining the antigen and alleles at a nearby locus which confers susceptibility to disease. We determined whether observed decreases in antigen frequencies among a patient group are simply the inevitable result of the fact that if one or more alleles at a locus is increased in frequency, then others must be decreased. Under the antigen predisposing model exact predictions concerning allele and antigen class frequencies at the predisposing locus, and the non-predisposing loci, are given. The predictions are examined using HLA-DR data for multiple sclerosis.
在两种模型下,从理论上研究了阴性和多种HLA抗原疾病关联的性质和程度。第一种模型假设HLA抗原直接参与使个体易患疾病。第二种模型假设特定HLA抗原与疾病的关联是决定该抗原的等位基因与附近赋予疾病易感性的位点上等位基因之间连锁不平衡的结果。我们确定了在患者群体中观察到的抗原频率下降是否仅仅是这样一个事实的必然结果:即如果一个位点上的一个或多个等位基因频率增加,那么其他等位基因频率必然下降。在抗原易患模型下,给出了关于易患位点和非易患位点上等位基因和抗原类频率的精确预测。使用多发性硬化症的HLA - DR数据对这些预测进行了检验。