Inamura N, Nakahara K, Kino T, Gotoh T, Kawamura I, Aoki H, Imanaka H, Sone S
J Biol Response Mod. 1985 Aug;4(4):408-17.
The effect of FK-565, a novel low molecular weight (MW) acyltripeptide, on tumoricidal properties of murine macrophages is reported here. Peritoneal macrophages (PMs) harvested from C57BL/6 mice and beige mice were rendered cytotoxic to syngeneic B16 melanoma cells following their interaction in vitro with FK-565. Maximal and reproducible activation of tumoricidal properties in PM were obtained by interaction in vitro with 25 micrograms/ml of FK-565 for a 24 h period, and as little as 0.5 microgram/ml of FK-565 was sufficient to induce significant cytotoxicity. Murine PMs activated by FK-565 in vitro were cytotoxic to syngeneic and xenogeneic tumor cells, but did not affect allogeneic nontumor cells. The PMs were also activated to kill B16 melanoma cells by intraperitoneal injections of FK-565 (10 mg/kg). Multiple injections of FK-565 into mice also slightly but significantly inhibited lung metastases. These results suggest that FK-565 has potential as an effective immunopotentiator in immunotherapy.
本文报道了一种新型低分子量(MW)酰基三肽FK-565对小鼠巨噬细胞杀肿瘤特性的影响。从C57BL/6小鼠和米色小鼠收集的腹腔巨噬细胞(PMs)在体外与FK-565相互作用后,对同基因B16黑色素瘤细胞产生细胞毒性。通过在体外与25微克/毫升的FK-565相互作用24小时,可在PM中获得最大且可重复的杀肿瘤特性激活,而低至0.5微克/毫升的FK-565就足以诱导显著的细胞毒性。体外经FK-565激活的小鼠PMs对同基因和异基因肿瘤细胞具有细胞毒性,但不影响同种异体非肿瘤细胞。通过腹腔注射FK-565(10毫克/千克),PMs也被激活以杀死B16黑色素瘤细胞。多次向小鼠注射FK-565也轻微但显著地抑制了肺转移。这些结果表明,FK-565在免疫治疗中具有作为有效免疫增强剂的潜力。