INHIBITORY-ACTION OF A (1-]6)-BETA-D-GLUCAN-PROTEIN COMPLEX (F-III-2-B) ISOLATED FROM AGARICUS-BLAZEI MURILL (HIMEMATSUTAKE) ON METH-A FIBROSARCOMA-BEARING MICE AND ITS ANTITUMOR MECHANISM

The effects of FIII-2-b (Agaricus blazei Murill polysaccharide) with or without 5-fluorouracil (5-FU) on immune responses were investigated in Meth A tumor-bearing and normal mice. The i.p. administration of FIII-2-b (10 mg/kg/day x 30) moderately inhibited the growth of Meth A tumor cells implanted s.c. in mice. Development of implanted tumors was strongly inhibited by the combination of FIII-2-b and 5-FU. The picryl chloride-induced delayed type hypersensitivity (PC-DTH) response in mice was depressed after the implantation of tumor and treatment with 5-FU. FIII-2-b restored the suppression of PC-DTH by 5-FU, but did not increase the PC-DTH of normal mice. FIII-2-b not only enhanced the degree of spleen cell-mediated sheep red blood cells (SRBC) hemolysis (quantitative hemolysis of SRBC), the indexes of the spleen and thymus, and the number of spleen cells but also restored the suppressive effect of 5-FU. In the group receiving FIII-2-b, the percentages of splenic Thy1.2-, L3T4- and asialo GM1-positive cells were significantly increased as compared with the tumor-bearing mice treated with saline. Furthermore, the L3T4(+)/Lyt2(+) ratio showed a tendency to increase, and the Lyt2(+)/Thy1.2(+) ratio was markedly decreased. These results suggest that the antitumor effect of FIII-2-b may be correlated with the changing pattern of the Thy1.2-, L3T4- and asialo GM1-positive cells.