Bruley-Rosset M, Florentin I, Khalil A M, Mathé G
Int Arch Allergy Appl Immunol. 1976;51(5):594-607. doi: 10.1159/000231638.
Six systemic adjuvants: living bacillus Calmette-Guérin (BCG), hydrosoluble extracts from BCG and from Mycobacterium smegmatis, bacterial lipopolysaccharide, lentinan and levamisole, have been tested for their ability to induce macrophage activation in mice. The first four adjuvants mentioned increase phosphatase activity of peritoneal macrophages and make them nonspecifically cytotoxic for tumor cells in vitro. The intensity of these phenomena vary with route and time of administration. In contrast, lentinan and levamisole depress both these macrophage activities. Living BCG, extracts from BCG and from M. smegmatis, and the lipopolysaccharide increase the cytotoxic potential of normal macrophages in vitro, suggesting that these agents may exert a direct action on macrophages. Levamisole did not activate normal macrophages in vitro. The existence of a correlation between the capacity of adjuvants to stimulate macrophage tumoricidal activity and their efficiency in active cancer immunotherapy is discussed.
活卡介苗(BCG)、卡介苗和耻垢分枝杆菌的水溶性提取物、细菌脂多糖、香菇多糖和左旋咪唑,已对它们在小鼠体内诱导巨噬细胞活化的能力进行了测试。上述前四种佐剂可提高腹膜巨噬细胞的磷酸酶活性,并使其在体外对肿瘤细胞具有非特异性细胞毒性。这些现象的强度随给药途径和时间而变化。相比之下,香菇多糖和左旋咪唑会抑制这两种巨噬细胞活性。活卡介苗、卡介苗和耻垢分枝杆菌的提取物以及脂多糖可增强正常巨噬细胞在体外的细胞毒性潜力,表明这些制剂可能对巨噬细胞产生直接作用。左旋咪唑在体外未激活正常巨噬细胞。文中讨论了佐剂刺激巨噬细胞杀肿瘤活性的能力与其在主动癌症免疫治疗中的效率之间的相关性。