Ball E J, Stastny P
Immunogenetics. 1984;20(5):547-64. doi: 10.1007/BF00364357.
Human T-cell lines responsive to the polypeptide antigens GAT and (T,G)-A--L were developed. They were specific for the priming antigens and required the participation of accessory cells matched for HLA-linked determinants, as shown in family studies. In panel studies, the ability of accessory cells to present antigen was shown to be associated with HLA-D-region antigens. However, the specificity of these determinants did not fully correspond to any HLA antigens as currently defined. One GAT-specific subline, derived by limiting dilution, utilized a restriction determinant associated with, but distinct from, the DQw3 (MB3) allospecificity. Blocking studies with mouse monoclonal antibodies indicated that this restriction determinant was carried by HLA-DQ molecules. The epitopes recognized in these molecules appear to be distinct from the alloantigenic determinants currently defined by serology.
已建立了对多肽抗原GAT和(T,G)-A--L有反应的人T细胞系。如家族研究所示,它们对引发抗原具有特异性,并且需要与HLA连锁决定簇相匹配的辅助细胞参与。在分组研究中,辅助细胞呈递抗原的能力与HLA-D区抗原相关。然而,这些决定簇的特异性并不完全对应于目前所定义的任何HLA抗原。通过有限稀释法获得的一个GAT特异性亚系利用了一种与DQw3(MB3)同种特异性相关但又不同的限制性决定簇。用小鼠单克隆抗体进行的阻断研究表明,这种限制性决定簇由HLA-DQ分子携带。在这些分子中识别的表位似乎与目前通过血清学定义的同种抗原决定簇不同。