C. Kudo et al., CURATIVE TREATMENTS OF MURINE COLON26 SOLID TUMORS BY IMMUNOCHEMOTHERAPY WITH G-CSF AND OK-432, Immunopharmacology, 29(3), 1995, pp. 235-243
In order to study the clinical usefulness of biological response modif
iers (BRMs) in eliminating malignant solid tumors, we have investigate
d the effect of various combination therapies on the murine Colon26 so
lid tumor model. When the tumor-bearing mice were treated with chemoth
erapeutics, G-CSF and OK-432 (streptococcal preparation), the tumors c
ompletely disappeared from all of the treated mice. When these survivo
rs were rechallenged with Colon26 tumor cells on Day 120, all of them
survived without showing any sign of reccurence or metastases. The res
ults indicate that mice with malignant solid tumors, which can not be
cured using chemotherapeutics alone, may be completely healed with a c
ombination immuno-chemotherapy. During the course of this combination
therapy study, it was found that there was a clear positive correlatio
n between immunosuppressive acidic protein (IAP) levels and tumor size
s. Suppressor macrophages (sM phi) which produce IAP were found to be
decreased in bone marrow and spleen of treated mice. This suggests tha
t 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 mic
e very effectively through not only synergistic direct tumor cell dest
ruction but also indirect immunomodulation of the host.