Lotze M T, Rosenberg S A
Immunobiology. 1986 Sep;172(3-5):420-37. doi: 10.1016/S0171-2985(86)80122-X.
The administration of transferred lymphokine-activated killer (LAK) cells in conjunction with the administration of recombinant interleukin 2 (IL 2) at high doses has led to objective remissions in 14/41 cancer patients. Sequential studies with both Jurkat-derived IL 2, recombinant IL 2 and activated cells were conducted in a total of sixty-seven patients with cancer which established the safety, toxicity and immunologic effects of these treatments prior to their successful combination in humans. This regimen was developed in pulmonary and hepatic metastases models in mice using a variety of transplantable tumors. More recently we have demonstrated both in mice and in patients with melanoma that very high doses of recombinant IL 2 (greater than 100,000 units/kg administered three times daily) can lead to objective regressions. The future development of these immunotherapies will include their evaluation in adjuvant settings as well as in combination with other conventional cancer treatments.
给予转移的淋巴因子激活的杀伤细胞(LAK)并同时大剂量给予重组白细胞介素2(IL-2),已使41例癌症患者中的14例出现客观缓解。对总共67例癌症患者进行了有关源自Jurkat细胞的IL-2、重组IL-2和活化细胞的序贯研究,这些研究在这些治疗成功用于人体之前确定了其安全性、毒性和免疫效应。该方案是在小鼠的肺和肝转移模型中使用多种可移植肿瘤制定的。最近,我们在小鼠和黑色素瘤患者中均证明,非常高剂量的重组IL-2(每日三次给予大于100,000单位/千克)可导致客观消退。这些免疫疗法的未来发展将包括在辅助治疗环境中以及与其他传统癌症治疗方法联合使用时对它们进行评估。