Yaita H, Yasumoto K, Nagashima A, Sugimachi K, Nomoto K
Second Department of Surgery, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
J Surg Oncol. 1988 Jul;38(3):165-72. doi: 10.1002/jso.2930380308.
Cytotoxic activities of regional lymph node lymphocytes (RLNL) and peripheral blood lymphocytes (PBL) of 49 primary lung cancer patients who were subjected to surgical resection were examined by 4 h 51Cr release assay. PBL showed significantly lower cytotoxicity against autologous tumor cells than against K562 and QG-56. On the other hand, RLNL exhibited the same level of cytotoxicity against autologous tumor cells as PBL, although the cytotoxicities against K562 and QG-56 were low. Cytotoxicity of RLNL against autologous tumor cells exhibited a significant degree of depression with the advance of stage, T and N factors. Cytotoxicity of PBL did not significantly change as the stage progressed. When both PBL and RLNL were cultured with purified interleukin-2 (p-IL2) in vitro, their cytotoxic activities were markedly augmented and the cytotoxicities could not be diminished by the treatment with anti-Leu-7 + anti-Leu-11b + C'. These facts indicate that the augmented cytotoxicity may be due to lymphokine activated killer (LAK) cells.
采用4小时51Cr释放试验检测了49例接受手术切除的原发性肺癌患者区域淋巴结淋巴细胞(RLNL)和外周血淋巴细胞(PBL)的细胞毒性活性。PBL对自体肿瘤细胞的细胞毒性显著低于对K562和QG-56的细胞毒性。另一方面,RLNL对自体肿瘤细胞的细胞毒性与PBL相同,尽管对K562和QG-56的细胞毒性较低。随着分期、T和N因子的进展,RLNL对自体肿瘤细胞的细胞毒性显著降低。随着分期进展,PBL的细胞毒性无显著变化。当PBL和RLNL在体外与纯化的白细胞介素-2(p-IL2)一起培养时,它们的细胞毒性活性显著增强,并且用抗Leu-7 +抗Leu-11b + C'处理不能降低细胞毒性。这些事实表明,增强的细胞毒性可能归因于淋巴因子激活的杀伤(LAK)细胞。