Asano T, Fujimaki W, McWatters A, An T, Matsushima K, Kleinerman E S
Department of Cell Biology, University of Texas M. D. Anderson Cancer Center, Houston 77030.
Cancer Immunol Immunother. 1993 Nov;37(6):408-11. doi: 10.1007/BF01526798.
Liposomal muramyl tripeptide phosphatidylethanolamine (L-MTP-PE) is a biological agent in phase I and II trials for osteosarcoma and melanoma. Its mechanism of action has been linked to its ability to activate monocyte tumoricidal function and to stimulate monocyte production of tumor necrosis factor (TNF) and interleukins(IL)-1, -6, and -8. Our ultimate goal is to combine L-MTP-PE with chemotherapy. The purpose of this study was to determine whether doxorubicin (Adriamycin) interfered with the ability of L-MTP-PE to activate monocyte cytokine production. Human monocytes were cultured with or without 5-500 ng/ml of Adriamycin for 3 h and washed before being exposed to 2 micrograms/ml L-MTP-PE for 16 h. Cultured supernatants were collected and assayed for TNF, IL-1, IL-6, and IL-8. The messenger RNA expression of IL-1 alpha, IL-1 beta, TNF alpha, IL-6, and IL-8 was quantified with northern blot analysis. Adriamycin did not suppress the up-regulation of any of these cytokines. We concluded that combination therapy with L-MTP-PE and Adriamycin is feasible and that this combination warrants further investigation in a clinical setting.
脂质体胞壁酰三肽磷脂酰乙醇胺(L-MTP-PE)是一种正在进行骨肉瘤和黑色素瘤I期和II期试验的生物制剂。其作用机制与其激活单核细胞杀瘤功能以及刺激单核细胞产生肿瘤坏死因子(TNF)和白细胞介素(IL)-1、-6和-8的能力有关。我们的最终目标是将L-MTP-PE与化疗联合使用。本研究的目的是确定阿霉素是否会干扰L-MTP-PE激活单核细胞产生细胞因子的能力。将人类单核细胞在含有或不含有5-500 ng/ml阿霉素的条件下培养3小时,然后洗涤,再暴露于2微克/毫升L-MTP-PE中16小时。收集培养上清液并检测其中的TNF、IL-1、IL-6和IL-8。用Northern印迹分析法定量检测IL-1α、IL-1β、TNFα、IL-6和IL-8的信使核糖核酸表达。阿霉素并未抑制这些细胞因子中的任何一种的上调。我们得出结论,L-MTP-PE与阿霉素联合治疗是可行的,这种联合疗法值得在临床环境中进一步研究。