Nakano K, Nakamura I, Cudkowicz G
J Immunol. 1981 Jul;127(1):173-8.
The immunogenetic specificity of (C57BL/6 X DBA/2)F1 anti-parental C57BL/6 cytotoxic T lymphocytes (CTL) induced in primary mixed spleen cell cultures was determined in direct lytic and competitive inhibition assays. A large panel of peritoneal exudate cells (PEC) bearing nonrecombinant and recombinant H-2-Tla haplotypes was the source of target and inhibitor cells. All PEC of H-2b, H-2bc, H-2j, and H-2ja types, irrespective of background genetic constitution, were as susceptible to direct lysis as C57BL/6 PEC, but PEC of H-2a, H-2d, H-2k, H-2q, H-2s, and H-2u types were not. The possible involvement of the Tla region in controlling target antigens was excluded by testing PEC obtained from 4 H-2/Tla or intra-Tla recombinant mouse strains. The genes controlling target antigens were mapped to the D region with the aid of 9 intra-H-2 recombinants; for target PEC to be lysed it was necessary and sufficient that Db antigens be part of the H-2 phenotype. These results were confirmed by competitive inhibition assays. Resident peritoneal cells not exposed to fetal bovine serum were also lysed by F1 anti-parental H-2b CTL, a demonstration that target antigens are expressed on normal cells.
在直接裂解和竞争抑制试验中,测定了在原代混合脾细胞培养物中诱导产生的(C57BL/6×DBA/2)F1抗亲本C57BL/6细胞毒性T淋巴细胞(CTL)的免疫遗传特异性。一大组带有非重组和重组H-2-Tla单倍型的腹腔渗出细胞(PEC)作为靶细胞和抑制细胞的来源。所有H-2b、H-2bc、H-2j和H-2ja型的PEC,无论背景遗传构成如何,与C57BL/6 PEC一样易受直接裂解,但H-2a、H-2d、H-2k、H-2q、H-2s和H-2u型的PEC则不然。通过检测从4种H-2/Tla或Tla内部重组小鼠品系获得的PEC,排除了Tla区域在控制靶抗原方面的可能作用。借助9种H-2内部重组体,将控制靶抗原的基因定位到D区域;对于要被裂解的靶PEC来说,Db抗原成为H-2表型的一部分是必要且充分的。这些结果通过竞争抑制试验得到了证实。未接触胎牛血清的驻留腹腔细胞也被F1抗亲本H-2b CTL裂解,这表明靶抗原在正常细胞上表达。