Tajima Y, Kojima H, Ishikawa N, Wakisaka A, Aizawa M
First Department of Pathology, Hokkaido University School of Medicine, Sapporo, Japan.
Tissue Antigens. 1987 Nov;30(5):204-12. doi: 10.1111/j.1399-0039.1987.tb01623.x.
Two Leu2(-), Leu3(+), Leu4(+) human cytotoxic T lymphocyte (CTL) clones, BE-11 and AF-3, were generated against Epstein-Barr virus (EBV)-transformed cell line GI (Dw8/DRw8/DQWa homozygous). Blocking experiments with various monoclonal antibodies (MoAbs) revealed that the former recognized the DR molecule and the latter recognized the DQ molecule, respectively. Panel studies showed that CTL clone BE-11 lysed not only DRw8-positive cells but also DR1-positive ones. CTL clone AF-3 exhibited cytotoxicity against only Dw8/DRw8/DQWa typed cells. Until now, such specificities have not been defined serologically or biochemically. These results demonstrated that the previously unknown DR and DQ specificities could be defined by CTL clones, suggesting that CTL clones might be especially valuable tools for investigating the structural polymorphism of HLA antigens.
针对爱泼斯坦-巴尔病毒(EBV)转化的细胞系GI(Dw8/DRw8/DQWa纯合子),产生了两个Leu2(-)、Leu3(+)、Leu4(+)人细胞毒性T淋巴细胞(CTL)克隆BE-11和AF-3。用各种单克隆抗体(MoAb)进行的阻断实验表明,前者识别DR分子,后者分别识别DQ分子。分组研究显示,CTL克隆BE-11不仅能裂解DRw8阳性细胞,还能裂解DR1阳性细胞。CTL克隆AF-3仅对Dw8/DRw8/DQWa分型的细胞表现出细胞毒性。到目前为止,这些特异性尚未通过血清学或生化方法确定。这些结果表明,以前未知的DR和DQ特异性可以通过CTL克隆来确定,这表明CTL克隆可能是研究HLA抗原结构多态性的特别有价值的工具。