CURATIVE TREATMENTS OF MURINE COLON26 SOLID TUMORS BY IMMUNOCHEMOTHERAPY WITH G-CSF AND OK-432

被引:4
作者
KUDO, C [1 ]
SAITO, M [1 ]
YOSHIDA, T [1 ]
机构
[1] TOKYO INST IMMUNOPHARMACOL,TOSHIMA KU,TOKYO 171,JAPAN
来源
IMMUNOPHARMACOLOGY | 1995年 / 29卷 / 03期
关键词
COLON26; IMMUNOCHEMOTHERAPY; G-CSF; OK-432; IAP; SUPPRESSOR MACROPHAGE;
D O I
10.1016/0162-3109(95)00060-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In order to study the clinical usefulness of biological response modifiers (BRMs) in eliminating malignant solid tumors, we have investigated the effect of various combination therapies on the murine Colon26 solid tumor model. When the tumor-bearing mice were treated with chemotherapeutics, G-CSF and OK-432 (streptococcal preparation), the tumors completely disappeared from all of the treated mice. When these survivors were rechallenged with Colon26 tumor cells on Day 120, all of them survived without showing any sign of reccurence or metastases. The results indicate that mice with malignant solid tumors, which can not be cured using chemotherapeutics alone, may be completely healed with a combination immuno-chemotherapy. During the course of this combination therapy study, it was found that there was a clear positive correlation between immunosuppressive acidic protein (IAP) levels and tumor sizes. Suppressor macrophages (sM phi) which produce IAP were found to be decreased in bone marrow and spleen of treated mice. This suggests that the combination therapy may make the mice recover from a suppressed immune state caused by sM phi. In conclusion, the combination therapy with chemotherapeutics and BRMs could cure the solid tumor-bearing mice very effectively through not only synergistic direct tumor cell destruction but also indirect immunomodulation of the host.
引用
收藏
页码:235 / 243
页数:9
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