Quantitative dose-response survival curves for mouse leukemic tumor cells in vivo became possible by means of the end-point dilution assay of Hewitt and Wilson (1959), whose results were later confirmed and extended by Berry and Andrews (1961). The loss of reproductive integrity with ionizing radiations thus determined provided quantitative evidence that mammalian tumor cell radiation response in vivo was similar to that of cells irradiated and assayed in vitro by colony-forming ability (Puck and Marcus, 1956). Additional evidence supporting the in vivo survival curves determined by the TD50 method, was provided by the fact that the regrowth of surviving leukemic cells irradiated in vitro could be predicted by cell survival based on the TD50 method and upon the length of life (survival time) of isologous animals receiving transplants of irradiated leukemic cells (Maruyama et al., 1967). In addition, the radiation dose required to render known numbers of leukemic cell nonviable (" sterilizing " dose or SD50 assay) correlated with the TD50 survival curve, provided the recipients were immunologically suppressed by prior whole-body irradiation before they were challenged with the irradiated tumor cells (Maruyama, 1967). In the latter studies it was found that intact animals which were not immunologically suppressed developed a smaller proportion of tumor takes than the pre-irradiated animals.In these experiments, a systematic study of the effect of recipient whole-body X-irradiation before challenge by tumor cells a t the end point of terminal dilution (TD50) assay was investigated. The purpose was to determine the effect and the contribution of weak host-resistance to the overall TD50 survival curve, and the relative effect upon the assay of cells sub-lethally injured by small and large doses of X-irradiation. These results are the subject of this report.
MATERIAL AND METHODS
AnimalsInbred C57BL/Ka mice about 8-12 weeks of age were used. In each experiment, all recipients were matched for age, sex and size. All animals are descendants of a brother-sister, single-line