Kanda T, Macchi M J, LaPan K, Darsley M, Appella E, Frelinger J A
Department of Microbiology and Immunology, University of North Carolina, Chapel Hill 27514.
J Immunogenet. 1988 Oct-Dec;15(5-6):295-305. doi: 10.1111/j.1744-313x.1988.tb00433.x.
We have utilized a group of MHC class I genes produced by in vitro recombination between Dp and Dd to study recognition of MHC class I molecules by cytolytic T cells (CTLs). Both polyclonal allo-specific and H-2-restricted CTLs require that alpha 1 and alpha 2 of the target class I molecule be derived from the same haplotype for efficient killing. By using T-cell lines we showed that within the bulk population there must exist a fraction of T cells which can recognize epitopes in alpha 1 or alpha 2. Critical residues for T-cell recognition have been identified using these chimeric genes.
我们利用了一组通过Dp和Dd之间的体外重组产生的MHC I类基因,来研究细胞毒性T细胞(CTL)对MHC I类分子的识别。多克隆同种异体特异性CTL和H-2限制性CTL都要求靶I类分子的α1和α2来自同一单倍型,才能有效杀伤。通过使用T细胞系,我们表明在总体细胞群中一定存在一部分T细胞,它们能够识别α1或α2中的表位。利用这些嵌合基因已经确定了T细胞识别的关键残基。