Maziarz R T, Burakoff S J, Reiss C S
Cell Immunol. 1986 Apr 15;99(1):279-86. doi: 10.1016/0008-8749(86)90235-2.
Hybrid human-murine major histocompatibility antigens have been constructed and expressed on the surface of both human RD and murine L cell lines after DNA mediated gene transfer. These antigens linked the polymorphic domains (alpha 1 and alpha 2) of H-2Kb and the carboxy-terminal domains (alpha 3, transmembrane, and intracellular) of HLA-A2. Previously we demonstrated that these antigens were serologically intact and were recognized by allospecific cytolytic T lymphocytes. However, the cell lines expressing the hybrid antigen were less well lysed than the native H-2Kb expressing cell lines. In this study, we extend these observations and demonstrate that virally restricted cytolytic T lymphocytes specific for vesicular stomatitis virus and for Sendai virus can recognize cell lines expressing the hybrid antigen, whether expressed on murine (L cell) or human (RD cell) lines. Furthermore, the data show a profound influence by the carboxy-terminal domains upon the polymorphic T-cell restricting epitopes.
通过DNA介导的基因转移,已构建出人类-小鼠杂种主要组织相容性抗原,并在人类RD细胞系和小鼠L细胞系的表面表达。这些抗原连接了H-2Kb的多态性结构域(α1和α2)和HLA-A2的羧基末端结构域(α3、跨膜和细胞内结构域)。此前我们证明这些抗原在血清学上是完整的,并且能被同种特异性细胞毒性T淋巴细胞识别。然而,表达杂种抗原的细胞系比表达天然H-2Kb的细胞系更不易被裂解。在本研究中,我们扩展了这些观察结果,并证明对水疱性口炎病毒和仙台病毒具有特异性的病毒限制性细胞毒性T淋巴细胞能够识别表达杂种抗原的细胞系,无论该抗原是在小鼠(L细胞)还是人类(RD细胞)系上表达。此外,数据显示羧基末端结构域对多态性T细胞限制性表位有深远影响。