Ricci F, De Filippi R, Riccardi C, Romani L, Giuliani A
Dip. Med. Sper. e Scienze Biochimiche, II Università di Roma, Italy.
Chemioterapia. 1987 Dec;6(6):403-9.
Cis-diamminedichloroplatinum (DDP) or cyclophosphamide (Cy) were given to mice bearing L1210 or LSTRA leukemia in H-2 compatible tumor-host combinations. Little anti-tumor activity was afforded by DDP against both leukemias inoculated in entirely histocompatible recipients. However, when the drug was given to mice incompatible for minor histocompatibility loci (MMHL) with the tumor, the efficacy of the treatment was markedly augmented and a substantial number of long-term survivors was found among BALB/c mice inoculated with L1210 cells. On the other hand, no difference in survival times was found between histocompatible or allogeneic mice inoculated with both leukemias, not subjected to chemotherapy. The LSTRA model was much less susceptible to this type of DDP-mediated antineoplastic immuno-chemotherapy synergism. Moreover no synergistic effects with allograft reaction were detected with Cy in both L1210 and LSTRA models, although Cy was markedly more active than DDP against leukemic cells in histocompatible recipients.
顺二氯二氨铂(DDP)或环磷酰胺(Cy)被给予在H-2相容的肿瘤-宿主组合中携带L1210或LSTRA白血病的小鼠。DDP对接种在完全组织相容性受体中的两种白血病几乎没有抗肿瘤活性。然而,当将该药物给予与肿瘤在次要组织相容性位点(MMHL)不相容的小鼠时,治疗效果显著增强,并且在接种L1210细胞的BALB/c小鼠中发现了大量长期存活者。另一方面,接种两种白血病且未接受化疗的组织相容性或同种异体小鼠之间的存活时间没有差异。LSTRA模型对这种DDP介导的抗肿瘤免疫化疗协同作用的敏感性要低得多。此外,在L1210和LSTRA模型中,均未检测到Cy与同种异体移植反应的协同效应,尽管在组织相容性受体中,Cy对白血病细胞的活性明显高于DDP。