Baba N, Kawami H, Sato Y, Takayama T, Toge T
Department of Surgery, Hiroshima University, Japan.
Biotherapy. 1991;3(4):359-64. doi: 10.1007/BF02221329.
The enhancement of antitumor activities of the tumoricidal soluble factor (SF) from a streptococcal preparation (OK-432)-activated macrophages by the pretreatment with a protein-bound polysaccharide (PSK) was investigated in tumor-bearing mice. Two-step stimulations with OK-432 at in vivo priming and in vitro eliciting were required for the production of the tumoricidal SF by macrophages, and the tumoricidal activity of the SF apparently correlated with the uptake of OK-432 by macrophages at priming phase. Tumoricidal activity of the SF from OK-432-activated macrophages in proteose-peptone (P-P)-pretreated mice significantly decreased with the development of the tumor, whereas in PSK-pretreated mice did not. Pretreatment of tumor-bearing mice with PSK saved a decrease in the macrophages carrying Iak or asialo GM1 antigens and an increase in wheat germ agglutinin (WGA) receptors. Furthermore, the uptake of OK-432 by macrophages at priming phase was enhanced. The tumoricidal activity of the SF from OK-432-activated macrophages was augmented. Thus, PSK may restore the depressed functions of macrophages, and the combination therapy with PSK and OK-432 may be effective to enhance the production of tumoricidal SF in tumor-bearing mice.
在荷瘤小鼠中研究了用蛋白结合多糖(PSK)预处理对链球菌制剂(OK-432)激活的巨噬细胞产生的杀肿瘤可溶性因子(SF)的抗肿瘤活性的增强作用。巨噬细胞产生杀肿瘤SF需要在体内启动和体外诱导时用OK-432进行两步刺激,并且SF的杀肿瘤活性显然与启动阶段巨噬细胞对OK-432的摄取相关。在蛋白胨(P-P)预处理的小鼠中,OK-432激活的巨噬细胞产生的SF的杀肿瘤活性随着肿瘤的发展而显著降低,而在PSK预处理的小鼠中则没有。用PSK预处理荷瘤小鼠可避免携带Iak或去唾液酸GM1抗原的巨噬细胞减少以及麦胚凝集素(WGA)受体增加。此外,启动阶段巨噬细胞对OK-432的摄取增强。OK-432激活的巨噬细胞产生的SF的杀肿瘤活性增强。因此,PSK可能恢复巨噬细胞的功能抑制,并且PSK与OK-432的联合治疗可能有效地增强荷瘤小鼠中杀肿瘤SF的产生。