Taguchi T, Domoto K
Gan To Kagaku Ryoho. 1987 Mar;14(3 Pt 2):914-21.
We have examined the effects of recombinant human interleukin-2 (rIL-2) on generation of lymphokine-activated killer (LAK) cells and adoptive immunotherapy. rIL-2 generated LAK activity dose- and time-dependently. The generated LAK cells by rIL-2 killed autologous and various allogenic tumor cells but not normal cells. No difference was found in the generation of LAK activity by rIL-2 between healthy donors and cancer patients rIL-2 generated LAK activity of lymphocytes obtained from peripheral blood, spleen, pleural fluid and ascites in cancer patients. Two cancer patients with pleuritis carcinomatosa, who had not responded to various chemotherapeutic agents, were treated with adoptive immunotherapy. LAK cells were generated from the lymphocytes of pleural fluid or peripheral blood incubated with rIL-2 (5 U/ml) for 5 days. LAK cells (0.1-1.0 X 10(9)/100 ml in total) were administered into the pleural cavity followed by injection of rIL-2 (1,000 U) 1 to 7 times. No significant adverse effect was observed except for fever and eosinophilia. Complete disappearance of pleural tumor cells was observed in one patient and decrease in the other.
我们研究了重组人白细胞介素 -2(rIL -2)对淋巴因子激活的杀伤(LAK)细胞生成及过继性免疫治疗的影响。rIL -2呈剂量和时间依赖性地产生LAK活性。rIL -2产生的LAK细胞可杀伤自体及多种异体肿瘤细胞,但不杀伤正常细胞。健康供者和癌症患者之间,rIL -2产生LAK活性的情况未发现差异。rIL -2可产生癌症患者外周血、脾脏、胸水和腹水中淋巴细胞的LAK活性。两名患有癌性胸膜炎且对多种化疗药物无反应的癌症患者接受了过继性免疫治疗。用rIL -2(5 U/ml)将胸水或外周血淋巴细胞孵育5天来产生LAK细胞。将LAK细胞(总量为0.1 - 1.0×10⁹/100 ml)注入胸腔,随后注射rIL -2(1000 U)1至7次。除发热和嗜酸性粒细胞增多外,未观察到明显的不良反应。一名患者胸腔肿瘤细胞完全消失,另一名患者肿瘤细胞减少。