Sandrelli A, De Fabritiis P, Di Nucci G D, Simone F, Di Matteo G, Mandelli F
Department of Human Biopathology, University La Sapienza, Roma, Italy.
J Biol Regul Homeost Agents. 1992 Jul-Sep;6(3):93-8.
In vitro antitumor effects of LAK cells and alpha-2b-Interferon (IFN) either alone or in combination were evaluated on NK resistant (K562) and NK sensitive (Namalwa, Raji) cell lines. Tumor cells were incubated with LAK cells for 4, 8 and 24 hours at a LAK: tumor cell ratio of 1:1, 10:1, 100:1, or with IFN for 48 and 96 h at the concentrations of 100, 1000, 10,000, 100,000 IU/ml. A clonogenic assay was utilised to enumerate residual cells after in vitro treatment. A positive correlation was found between tumor cell killing and effector: target ratio, IFN of 100:1 incubated for 4 h, and 100 IU/ml of IFN incubated for 48 h were further chosen. A synergistic effect was found when IFN was incubated before LAK cells or contemporarily, but not when IFN was incubated after LAK cells. These findings demonstrate that an additive or a synergistic effect in vitro can be obtained by adding the two agents in different sequences and suggest that a potential utility of LAK cells and IFN in vivo should be tested in clinical trials.
评估了LAK细胞和α-2b干扰素(IFN)单独或联合使用对NK抗性(K562)和NK敏感(Namalwa、Raji)细胞系的体外抗肿瘤作用。肿瘤细胞与LAK细胞以1:1、10:1、100:1的LAK:肿瘤细胞比例孵育4、8和24小时,或与IFN以100、1000、10000、100000 IU/ml的浓度孵育48和96小时。采用克隆形成试验来计数体外处理后的残留细胞。发现肿瘤细胞杀伤与效应细胞:靶细胞比例之间存在正相关,进一步选择100:1的LAK细胞孵育4小时以及100 IU/ml的IFN孵育48小时。当IFN在LAK细胞之前或同时孵育时发现有协同作用,但在LAK细胞之后孵育IFN时则没有。这些发现表明,通过以不同顺序添加这两种药物可在体外获得相加或协同作用,并提示LAK细胞和IFN在体内的潜在效用应在临床试验中进行测试。