Kimura H, Yamaguchi Y
Department of Surgery, School of Medicine, Chiba University.
Jpn J Clin Oncol. 1989 Sep;19(3):222-8.
Comparative cytotoxic activity and specificity studies of lymphokine activated killer (LAK) cells from different sources and preparations were carried out. Cytotoxic studies of lymphocytes from regional lymph nodes (Rn-LAK), peripheral blood (Pb-LAK) and those stimulated by autologous tumor cells and then activated by recombinant interleukine 2 (St-LAK) against autologous lung cancer cells, were conducted using the 51Cr-releasing test. The cytotoxic activities of these three LAK cells against autologous fibroblasts, allogeneic tumor cells, K-562 and Daudi cells were also compared. A time course experiment disclosed that the cytotoxic activity of Pb-LAK cells against autologous tumor cells reached a maximum on day 3 and declined shortly after the peak while that of Rn-LAK cells gradually increased to a maximum on day 7 and remained at a high titer for at least two weeks. The cytotoxic activity of Rn-LAK cells was significantly higher than that of Pb-LAK cells in seven out of 10 individual experiments and that of stimulated LAK (St-LAK) cells was higher than the cytotoxic activities of the other LAK cells in eight out of nine experiments. A specificity study showed that Rn-LAK cells possessed a higher cytotoxic activity against autologous tumor cells and a lower cytotoxic activity against autologous fibroblasts and allogeneic tumor cells than Pb-LAK cells. A comparative study of cytotoxic activities against K-562, Daudi cells and autologous tumor cells between St- and Rn-LAK cells demonstrated that although there was no difference in natural killer activity, cytotoxic activity against autologous tumor cells as well as the LAK activity of St-LAK cells were higher than that of Rn-LAK cells. These results indicate that the activities and specificities of LAK cells differ according to their source and preparation.
对来自不同来源和制剂的淋巴因子激活的杀伤(LAK)细胞的细胞毒性活性和特异性进行了比较研究。使用51Cr释放试验,对来自区域淋巴结(Rn-LAK)、外周血(Pb-LAK)的淋巴细胞以及那些由自体肿瘤细胞刺激然后由重组白细胞介素2激活的淋巴细胞(St-LAK)针对自体肺癌细胞的细胞毒性进行了研究。还比较了这三种LAK细胞对自体成纤维细胞、同种异体肿瘤细胞、K-562和Daudi细胞的细胞毒性活性。一项时间进程实验表明,Pb-LAK细胞对自体肿瘤细胞的细胞毒性活性在第3天达到最大值,并在峰值后不久下降,而Rn-LAK细胞的细胞毒性活性在第7天逐渐增加到最大值,并在至少两周内保持在高滴度。在10个个体实验中的7个实验中,Rn-LAK细胞的细胞毒性活性显著高于Pb-LAK细胞,在9个实验中的8个实验中,刺激的LAK(St-LAK)细胞的细胞毒性活性高于其他LAK细胞。一项特异性研究表明,与Pb-LAK细胞相比,Rn-LAK细胞对自体肿瘤细胞具有更高的细胞毒性活性,对自体成纤维细胞和同种异体肿瘤细胞具有更低的细胞毒性活性。对St-LAK细胞和Rn-LAK细胞针对K-562、Daudi细胞和自体肿瘤细胞的细胞毒性活性的比较研究表明,虽然自然杀伤活性没有差异,但St-LAK细胞对自体肿瘤细胞的细胞毒性活性以及LAK活性高于Rn-LAK细胞。这些结果表明,LAK细胞的活性和特异性因其来源和制剂而异。