Ting C C, Rodgigues D, Bushar G S, Herberman R B
J Immunol. 1976 Jan;116(1):236-43.
The primary cell-mediated cytotoxic response to a Friend virus-induced leukemia, FBL-3, in C57BL/6 mice was measured by the 125IUdR release assay. Intraperitoneal (i.p.) inoculation of 1 x 10(1) FBL-3 cells produced progressive tumor growth (progressors); subcutaneous (s.c.) inoculation of as many as 5 x 10(6) FBL-3 cells produced only transient tumor growth (regressors), and these mice would subsequently resist i.p. challenge of FBL-3 cells at 3 days after s.c. inoculation. The kinetics of the primary cell-mediated cytotoxic response of regressors was biphasic. Significant cytotoxicity could be detected at 3 to 5 days after s.c. inoculation of 5 x 10(6) FBL-3 cells peaked at days 10 to 14, declined to a very low level or became undetectable around days 20 to 30; then the reactivity reappeared and persisted at least up to 60 days. In progressors, the kinetics of the cell-mediated cytotoxic response was similar to the regressors, but the reactivity was much lower. The cytotoxic response was found to be T cell dependent, during both the first peak (days 10 to 14) and the second peak (days 40 to 60). In adoptive transfer experiments, lymphocytes from regressors gave 90% protection against i.p. challenge of FBL-3; lymphocytes from progressors only gave 40% protection.
通过¹²⁵IUdR释放试验测定了C57BL/6小鼠对Friend病毒诱导的白血病FBL-3的原发性细胞介导的细胞毒性反应。腹腔内(i.p.)接种1×10¹个FBL-3细胞会导致肿瘤进行性生长(进展型);皮下(s.c.)接种多达5×10⁶个FBL-3细胞仅产生短暂的肿瘤生长(消退型),并且这些小鼠在皮下接种后3天会随后抵抗FBL-3细胞的腹腔内攻击。消退型小鼠原发性细胞介导的细胞毒性反应动力学呈双相性。在皮下接种5×10⁶个FBL-3细胞后3至5天可检测到显著的细胞毒性,在第10至14天达到峰值,在第20至30天左右降至非常低的水平或变得无法检测到;然后反应性再次出现并至少持续到60天。在进展型小鼠中,细胞介导的细胞毒性反应动力学与消退型小鼠相似,但反应性要低得多。发现在第一个峰值(第10至14天)和第二个峰值(第40至60天)期间,细胞毒性反应均依赖于T细胞。在过继转移实验中,来自消退型小鼠的淋巴细胞对FBL-3的腹腔内攻击提供了90%的保护;来自进展型小鼠的淋巴细胞仅提供了40%的保护。