Fidler I J, Darnell J H, Budmen M B
Cancer Res. 1976 Oct;36(10):3608-15.
Macrophage-activating factor (MAF) was obtained from cultures of normal F344 rat lymphocytes incubated with insoluble concanavalin A. The MAF rendered macrophages from normal C57BL/6 mice cytotoxic against the syngeneic B16 melanoma and the allogeneic AC 15091. At the same time, normal syngeneic or allogeneic embryo cells were unharmed, even in the presence of susceptible tumor cells. Optimal MAF levels followed incubation of lymphocytes for 48 hr with Sepharose-bound concanavalin A. A 2-hr incubation of macrophages with MAF was sufficient to initiate activation, providing that 46 hr were allowed to elapse before tumor cells were added. The MAF activity was enhanced after heating the supernatant to 199 degrees. Control experiments largely excluded the possibility that residual unbound concanavalin A caused the observed macrophage-mediated tumoricidal effects.
巨噬细胞激活因子(MAF)是从与不溶性伴刀豆球蛋白A孵育的正常F344大鼠淋巴细胞培养物中获得的。该MAF使正常C57BL/6小鼠的巨噬细胞对同基因B16黑色素瘤和异基因AC 15091具有细胞毒性。同时,正常的同基因或异基因胚胎细胞不受损害,即使在存在易感肿瘤细胞的情况下也是如此。淋巴细胞与琼脂糖结合的伴刀豆球蛋白A孵育48小时后可达到最佳MAF水平。巨噬细胞与MAF孵育2小时足以启动激活,前提是在添加肿瘤细胞之前允许经过46小时。将上清液加热到199度后,MAF活性增强。对照实验在很大程度上排除了残留未结合的伴刀豆球蛋白A导致观察到的巨噬细胞介导的杀肿瘤作用的可能性。