Nakatsuji T, Inoko H, Ando A, Sato T, Koide Y, Tadakuma T, Yoshida T O, Tsuji K
Immunogenetics. 1987;25(1):1-6. doi: 10.1007/BF00768826.
DR gene products are commonly thought to be involved in the induction of the mixed lymphocyte reaction (MLR). However, very little is known about the role of HLA-DQ antigens in the MLR. To address this question, we introduced DQ alpha and beta chain genes into mouse L cells, a human T-cell line, and a human premonocytoid cell line using a liposome-mediated transfer technique. The DQ alpha and DQ beta genomic clones were isolated from a DR2 DQw1 and a DR3 DQw2 phage library, respectively. The pSV2-Neo gene was introduced as a selection marker with both DQ alpha and DQ beta. The resultant transfected cells were able to bind several HLA class II monoclonal antibodies. In addition, these cells were found to be efficient in stimulating peripheral blood lymphocyte proliferation under MLR-like conditions, implying a role for HLA-DQ molecules in HLA-D typing differences.
DR基因产物通常被认为参与混合淋巴细胞反应(MLR)。然而,关于HLA - DQ抗原在MLR中的作用却知之甚少。为了解决这个问题,我们使用脂质体介导的转移技术将DQα和β链基因导入小鼠L细胞、一种人T细胞系和一种人前单核细胞系。DQα和DQβ基因组克隆分别从DR2 DQw1和DR3 DQw2噬菌体文库中分离得到。pSV2 - Neo基因作为选择标记与DQα和DQβ一起导入。所得的转染细胞能够结合几种HLAⅡ类单克隆抗体。此外,发现这些细胞在类似MLR的条件下能有效刺激外周血淋巴细胞增殖,这意味着HLA - DQ分子在HLA - D分型差异中起作用。