Kleinerman E S, Erickson K L, Schroit A J, Fogler W E, Fidler I J
Cancer Res. 1983 May;43(5):2010-4.
Peripheral blood monocytes were isolated from normal human donors by separation on a continuous Percoll gradient and adherence to yield preparations of blood monocytes with a high degree of purity (greater than 99%). The monocytes were incubated in vitro with medium alone or with multilamellar liposomes that contained either a lipophilic derivative of muramyl dipeptide, muramyl tripeptide (MTP-PE), or medium. The cytotoxic properties of the monocytes were assessed by an in vitro radioisotope release assay against various allogeneic targets. Monocytes that have phagocytosed liposomes containing MTP-PE were rendered tumoricidal. These monocytes lysed cells of three different tumorigenic lines but not cells of two nontumorigenic lines. The ability of MTP-PE-activated human blood monocytes to recognize and selectively lyse neoplastic cells was also demonstrated under cocultivation conditions. We conclude that human blood monocytes can be rendered tumoricidal after interaction with liposomes containing MTP-PE.
通过在连续的Percoll梯度上分离并贴壁,从正常人类供体中分离出外周血单核细胞,以获得高纯度(大于99%)的血液单核细胞制剂。将单核细胞在体外单独与培养基或与含有胞壁酰二肽的亲脂性衍生物、胞壁酰三肽(MTP-PE)或培养基的多层脂质体一起孵育。通过针对各种同种异体靶标的体外放射性同位素释放试验评估单核细胞的细胞毒性特性。吞噬含有MTP-PE脂质体的单核细胞具有杀肿瘤作用。这些单核细胞裂解了三种不同致瘤细胞系的细胞,但未裂解两种非致瘤细胞系的细胞。在共培养条件下也证明了MTP-PE激活的人血单核细胞识别并选择性裂解肿瘤细胞的能力。我们得出结论,人血单核细胞与含有MTP-PE的脂质体相互作用后可具有杀肿瘤作用。