Mnatsakanian Iu A, Pospelov L E, Egorov I K
Genetika. 1977;13(1):64-9.
Three mutants of the H-2K gene within the mouse major histocompatibility complex were studied. Antisera anti-H-2.5 + 39 were unable to agglutinate H-2ba and H-2bf mutant red blood cells. The same sera moderately agglutinated H-2b red blood cells. The H-2ba red blood cells did not absorb in vitro the activity from an anti-H-2.5 serum, while the H-2b cells did. Thus, these results indicate the existence of qualitative SD antigenic differences among H-2Kb derived mutants. In the proliferative graft versus host test the H-2ba spleen cells did not induce spleen enlargement in the H-2bd recipients, while pronounced reaction was recovered in bd-ba combination. The (baXb) F1 hybrid cells were as efficient as b/b homozygous cells. The data suggest that the H-2K gene product may be involved in the antigen recognition process by T cells.
对小鼠主要组织相容性复合体内H-2K基因的三个突变体进行了研究。抗H-2.5 + 39抗血清无法凝集H-2ba和H-2bf突变体红细胞。相同的血清能适度凝集H-2b红细胞。H-2ba红细胞在体外不能吸收抗H-2.5血清的活性,而H-2b细胞可以。因此,这些结果表明源自H-2Kb的突变体之间存在定性的SD抗原差异。在增殖性移植物抗宿主试验中,H-2ba脾细胞在H-2bd受体中未诱导脾肿大,而在bd-ba组合中则出现明显反应。(baXb) F1杂交细胞与b/b纯合细胞一样有效。数据表明H-2K基因产物可能参与T细胞的抗原识别过程。