Jacobs S K, Wilson D J, Kornblith P L, Grimm E A
Cancer Res. 1986 Apr;46(4 Pt 2):2101-4.
In a Phase I study, recombinant interleukin-2 (IL-2) or autochthohous lymphokine-activated killer (LAK) cells were used to treat nine patients with malignant glioma. One patient received the combination of IL-2 and LAK cells. LAK cells were generated by culturing IL-2 with peripheral blood lymphocytes obtained from brain tumor patients. Escalating doses of LAK cells (10(8)-10(10) or recombinant IL-2 (10(4)-10(6) units) were administered by direct injection into the brain tissue surrounding the cavity left following operative tumor removal. There have been no signs of systemic or neurotoxicity following treatment. The tumor selective killing of the LAK cells used for these treatments was demonstrated by their ability to lyse glioma cells but not normal cells in vitro using a chromium release microcytotoxicity assay.
在一项I期研究中,使用重组白细胞介素-2(IL-2)或自体淋巴因子激活的杀伤细胞(LAK)治疗9例恶性胶质瘤患者。1例患者接受了IL-2和LAK细胞的联合治疗。LAK细胞通过用从脑肿瘤患者获得的外周血淋巴细胞培养IL-2产生。递增剂量的LAK细胞(10⁸ - 10¹⁰)或重组IL-2(10⁴ - 10⁶单位)通过直接注射到手术切除肿瘤后留下的腔周围的脑组织中给药。治疗后未出现全身或神经毒性迹象。用于这些治疗的LAK细胞对肿瘤的选择性杀伤作用通过其在体外使用铬释放微量细胞毒性试验裂解胶质瘤细胞而不裂解正常细胞的能力得到证明。