Eggermont A M, Sugarbaker P H, Marquet R L, Jeekel J
Cancer Immunol Immunother. 1987;25(1):16-24. doi: 10.1007/BF00199296.
We have previously shown that the in vivo administration of ABPP, an interferon inducing pyrimidinone, generates activated killer cells that can lyse fresh tumor cells in vitro in 4-h 51chromium release assays. The administration of this agent however has no effect on established tumor. In this communication we show that ABPP, when used in combination with low or moderate doses of cyclophosphamide, can be quite effective against early established (day 3) tumor as well as against advanced, grossly visible (day 8-10) tumor in both the i.p. and pulmonary metastasis model. The synergistic antitumor activity of this chemoimmunotherapeutic regimen was very strong against immunogenic tumors but rather weak against nonimmunogenic tumors. Two treatment cycles were significantly more effective than one and multiple cycles even cured the majority of mice with established i.p. tumor. These experiments demonstrate the potential of chemoimmunotherapeutic regimens and highlight the efficacy of multiple treatment cycles.
我们之前已经表明,体内给予ABPP(一种诱导干扰素的嘧啶酮)可产生活化的杀伤细胞,这些细胞在4小时的51铬释放试验中能够在体外裂解新鲜肿瘤细胞。然而,给予这种药物对已形成的肿瘤没有影响。在本通讯中,我们表明,ABPP与低剂量或中等剂量的环磷酰胺联合使用时,在腹腔内和肺转移模型中,对早期形成(第3天)的肿瘤以及晚期肉眼可见(第8 - 10天)的肿瘤都相当有效。这种化学免疫治疗方案的协同抗肿瘤活性对免疫原性肿瘤非常强,但对非免疫原性肿瘤相当弱。两个治疗周期比一个治疗周期显著更有效,多个周期甚至治愈了大多数患有已形成腹腔内肿瘤的小鼠。这些实验证明了化学免疫治疗方案的潜力,并突出了多个治疗周期的疗效。