Klein J, Forman J, Hauptfeld V, Egorov I K
J Immunol. 1975 Sep;115(3):716-8.
Mutation M523 (H-2ka) occurred spontaneously in strain CBA/CaLacSto and was discovered during routine skin graft testing for genetic homogeneity. By linkage and complementation tests, the mutation was previously mapped in the K end of the H-2 complex. We demonstrate that the mutation occurred in the K region, without affecting the I region in the K end of the complex. The mutant antigens cause rejection of skin grafts, stimulate cells in mixed lymphocyte culture, and function as stimulators as well as targets in cell-mediated lymphocytotoxicity. Yet, they are serologically indistinguishable from the antigens of the original strain and do not induce formation of humoral antibodies upon immunization of the CBA strain. Together with the results obtained on testing of other H-2 mutants, the data strongly support the notion that classical H-2 antigens (i.e., products of the H-2K and H-2D loci) can function as lymphocyte-stimulating determinants, and that I-region differences are not required for the induction of strong cell-mediated lymphocytotoxicity.
突变体M523(H-2ka)在CBA/CaLacSto品系中自发产生,是在进行遗传同质性的常规皮肤移植测试时发现的。通过连锁和互补试验,该突变先前被定位在H-2复合体的K端。我们证明该突变发生在K区域,而不影响复合体K端的I区域。突变抗原可引起皮肤移植排斥反应,刺激混合淋巴细胞培养中的细胞,并在细胞介导的淋巴细胞毒性中作为刺激物和靶标发挥作用。然而,它们在血清学上与原始品系的抗原无法区分,并且在对CBA品系进行免疫时不会诱导体液抗体的形成。连同对其他H-2突变体测试所获得的结果,这些数据有力地支持了以下观点:经典的H-2抗原(即H-2K和H-2D基因座的产物)可作为淋巴细胞刺激决定簇发挥作用,并且诱导强烈的细胞介导的淋巴细胞毒性不需要I区域的差异。