Koshimura S, Ryoyama K
Cancer Treat Rep. 1977 Jan-Feb;61(1):17-27.
OK-432, a streptococcal preparation with potent antitumor activity, has been evaluated for its efficacy in experimental and clincal trials. This preparation, however, was ineffective against mouse L1210 leukemia in all treatment schedules. The results of this study indicate that treatments with OK-432 and nucleic acid antimetabolites, such as 5-fluorouracil (5-FU), exert a synergistic effect against L1210 leukemia probably in conjunction with the immunologic defenses of the host. This therapeutic synergism was to some extent dependent on the dose level of 5-FU and was not produced against the 5-FU-resistant L1210 subline. In mice pre-treated with OK-432 prior to the leukemia implantation, there was no synergistic effect as a result of post-treatment with 5-FU. When BDF mice had previously received X-ray irradiation or administration of corticosteroids, the synergism could not be expected either. Comparative combination therapy with BCG or group C streptococcus resulted in failure to produce therapeutic synergism in this system.
OK-432是一种具有强大抗肿瘤活性的链球菌制剂,已在实验和临床试验中评估了其疗效。然而,该制剂在所有治疗方案中对小鼠L1210白血病均无效。本研究结果表明,用OK-432和核酸抗代谢物(如5-氟尿嘧啶(5-FU))进行治疗,可能与宿主的免疫防御协同作用,对L1210白血病发挥协同效应。这种治疗协同作用在一定程度上取决于5-FU的剂量水平,对5-FU耐药的L1210亚系未产生协同作用。在白血病植入前用OK-432预处理的小鼠中,5-FU后处理未产生协同效应。当BDF小鼠先前接受过X射线照射或给予皮质类固醇时,也无法预期会产生协同作用。在该系统中,与卡介苗或C组链球菌进行的比较联合治疗未能产生治疗协同作用。