Tanigaki N, Tosi R, Pressman D, Ferrara G B
Immunogenetics. 1980;10(2):151-67. doi: 10.1007/BF01561564.
Human Ia(-like) specificities controlled by gene loci other than HLA-DR were searched for at the molecular level in cells of human B-cell-type cell lines which carry two established DR specificities. Chevalier cells of DRw3 and 7 and U698M cells of DRw2 and 4 were used. Their Ia molecules were partially purified, radioiodinated and analyzed for Ia specificities by the direct binding and sequential binding assays with a selected panel of human Ia alloantisera. It was possible in both the cell lines to define a third subset of Ia molecules carrying a new specificity in addition to two Ia subsets carrying the established DR specificities. The new specificity was detected by putative anti-DRw4 and anti-DRw7 antisera and was closely associated with DRw4 and DRw7 at population level. It was thus designated provisionally as BR4X7. These results suggest that the BR4X7 specificity is coded for by a separate Ia locus closely linked to HLA-DR locus. The determinant(s) responsible for BR4X7 was located on the small subunit of Ia molecules.
在携带两种已确定的DR特异性的人B细胞型细胞系的细胞中,在分子水平上寻找由HLA - DR以外的基因座控制的人Ia(类)特异性。使用了DRw3和7的Chevalier细胞以及DRw2和4的U698M细胞。它们的Ia分子被部分纯化、放射性碘化,并通过与一组选定的人Ia同种抗血清进行直接结合和顺序结合试验来分析Ia特异性。在这两种细胞系中,除了携带已确定的DR特异性的两个Ia亚群外,还可能定义携带新特异性的第三个Ia分子亚群。新特异性由推定的抗DRw4和抗DRw7抗血清检测到,并且在群体水平上与DRw4和DRw7密切相关。因此,它被暂时命名为BR4X7。这些结果表明,BR4X7特异性由与HLA - DR基因座紧密连锁的一个单独的Ia基因座编码。负责BR4X7的决定簇位于Ia分子的小亚基上。