Fossati G, Holden H T, Herberman R B
Cancer Res. 1975 Sep;35(9):2600-8.
The cell-mediated immune response of C57BL/6 mice to murine sarcoma virus (MSV) was examined by the [125I]-iododeoxyuridine release cytotoxicity assay using MSV-induced sarcoma tissue culture cell lines as target cells. Cellular cytotoxicity was detected as early as 3 days after virus inoculation. Most mice assayed between 12 and 17 days after MSV inoculation gave positive results with maximum levels of activity present on Days 13 and 14. Reactivity was frequently detected for up to 100 days after MSV inoculation, although at low levels (5 to 10%). Additional experiments comparing the kinetics of the cellular response as measured by different in vitro cytotoxicity assays were performed. The results showed a good direct correlation between the [125I]iododeoxyuridine release assay and a 51Cr release assay. A similar pattern of reactivity was also observed when the cellular response was measured by a visual microcytotoxicity assay, although reactivity dropped off more rapidly and became undetectable in most instances by 20 days after injection of MSV. Studies on effector cell type revealed that cytotoxicity in all three assays was T-cell dependent, being eliminated by treatment with anti-theta plus complement. Macrophages did not appear to play a role, since treatment with carbonyl iron and magnet had no effect.
采用[125I] - 碘脱氧尿苷释放细胞毒性测定法,以鼠肉瘤病毒(MSV)诱导的肉瘤组织培养细胞系作为靶细胞,检测了C57BL/6小鼠对MSV的细胞介导免疫反应。在病毒接种后3天就检测到了细胞毒性。在MSV接种后12至17天检测的大多数小鼠都呈阳性结果,在第13天和第14天活性水平最高。尽管在MSV接种后长达100天仍能检测到反应性,但水平较低(5%至10%)。进行了其他实验,比较了通过不同体外细胞毒性测定法测量的细胞反应动力学。结果表明,[125I]碘脱氧尿苷释放测定法与51Cr释放测定法之间存在良好的直接相关性。当通过视觉微量细胞毒性测定法测量细胞反应时,也观察到了类似的反应模式,尽管反应性下降得更快,并且在注射MSV后20天在大多数情况下变得无法检测到。对效应细胞类型的研究表明,所有三种测定法中的细胞毒性均依赖于T细胞,用抗θ加补体处理可消除这种毒性。巨噬细胞似乎没有发挥作用,因为用羰基铁和磁铁处理没有效果。