Inada T, Uetake H
Infect Immun. 1978 Apr;20(1):1-5. doi: 10.1128/iai.20.1.1-5.1978.
Immune spleen cells (ISC) from mice immunized with a sublethal dose of mouse adenovirus (M-Ad) were shown by the 51Cr release test to be cytotoxic to target mouse embryonic cells or lymphoid cells infected with M-Ad. The number of ISC required for release of statistically significant amounts of 51Cr from target cells varied from one sample to another, ranging from 5 to greater than or equal to 30 ISC per target cell. When 24-h-infected mouse embryonic cells were used as targets, the release of 51Cr became evident in 6 h after the addition of ISC to the cells, gradually increased with time, and then leveled off. Cytolytic activity of M-Ad ISC is specific for M-Ad, since ISC do not lyse mouse embryonic cells infected with human adenovirus type 12 and vice versa. Kinetic study of the development of cell-mediated immunity to M-Ad assayed by 51Cr release showed that cytolytic activity of ISC in infected mice became detectable 4 days postinfection, reached its peak level about 7 to 10 days postinfection, and fell to undetectable levels about 10 days thereafter. This is consistent with the data obtained by inhibition of intracellular viral antigen synthesis or by the macrophage migration inhibition test in our prevous reports.
用亚致死剂量小鼠腺病毒(M-Ad)免疫的小鼠免疫脾细胞(ISC),通过51Cr释放试验表明对感染M-Ad的靶小鼠胚胎细胞或淋巴细胞具有细胞毒性。从靶细胞释放具有统计学显著量的51Cr所需的ISC数量因样品而异,每个靶细胞范围为5至大于或等于30个ISC。当使用感染24小时的小鼠胚胎细胞作为靶细胞时,在将ISC加入细胞后6小时51Cr的释放变得明显,随时间逐渐增加,然后趋于平稳。M-Ad ISC的细胞溶解活性对M-Ad具有特异性,因为ISC不会裂解感染人12型腺病毒的小鼠胚胎细胞,反之亦然。通过51Cr释放测定的针对M-Ad的细胞介导免疫发展的动力学研究表明,感染小鼠中ISC的细胞溶解活性在感染后4天可检测到,在感染后约7至10天达到峰值水平,并在之后约10天降至不可检测水平。这与我们之前报告中通过抑制细胞内病毒抗原合成或巨噬细胞迁移抑制试验获得的数据一致。