Stastny P, Ball E J, Khan M A, Olsen N J, Pincus T, Gao X
Br J Rheumatol. 1988;27 Suppl 2:132-8. doi: 10.1093/rheumatology/xxvii.suppl_2.132.
In a new series of RA patients the association with HLA-DR4 was again found to be highly significant. Also increased were the DR4 associated antigens DRw53 and DQw3. Hybridization of a DQ-beta probe to Bg1 II-digested DNA showed that a variant of DQw3, characterized by a 4.3 kb fragment and related to the serological specificity TA10, was markedly increased among DR4 positive RA patients. HLA-DR1 was also increased in RA and appeared to be independent of the increase of DR4. Although the DR1 association was weaker, it was observed in both patients with and without RF. In contrast, DR4 was found to be increased significantly only in the RF positive group of patients, as previously observed. Development of RA in multiple-case families was found to be linked to the inheritance of DR4 positive haplotypes. The possible role of risk factors associated with polymorphic markers of the T-cell receptor genes was investigated. An allelic marker associated with one of the variable gene subfamilies of the beta-chain was found to be associated with RA. The results suggest that susceptibility for development of RA is influenced by alleles of the T-cell receptor in conjunction with the class II HLA factors with which the T-cell receptor interacts in the course of the immune response.
在一组新的类风湿关节炎(RA)患者中,再次发现与HLA - DR4的关联具有高度显著性。与DR4相关的抗原DRw53和DQw3也有所增加。用DQ - β探针与Bg1 II酶切的DNA进行杂交显示,在DR4阳性的RA患者中,一种以4.3 kb片段为特征且与血清学特异性TA10相关的DQw3变体显著增加。HLA - DR1在RA患者中也有所增加,且似乎与DR4的增加无关。尽管DR1的关联性较弱,但在有和没有类风湿因子(RF)的患者中均有观察到。相比之下,正如之前所观察到的,DR4仅在RF阳性的患者组中显著增加。在多病例家庭中,RA的发病被发现与DR4阳性单倍型的遗传有关。研究了与T细胞受体基因多态性标记相关的危险因素的可能作用。发现与β链可变基因亚家族之一相关的一个等位基因标记与RA有关。结果表明,RA发病的易感性受T细胞受体等位基因以及在免疫反应过程中与T细胞受体相互作用的II类HLA因子的影响。