Morikawa Y, Watanabe S, Kodama T
Jpn J Clin Oncol. 1987 Jun;17(2):129-39.
The cytotoxic activities, of the peripheral blood lymphocytes (PBL) and regional lymph node lymphocytes (LNL) generated by incubation with recombinant IL-2 (rIL-2) in vitro, have been studied to assess their effects on autologous pulmonary adenocarcinoma cells from 21 patients with lung cancer. The lymphokine-activated killer (LAK) activities of PBL were 22.9 +/- 14.8% for autologous pulmonary adenocarcinoma cells and 44.9 +/- 20% for PC-9 cells. A previous coculture of autologous tumor cells with PBL (ATS-LAK) showed no increase in induction of cytotoxicity to autologous tumor cells. The LAK activities of LNL were significantly lower than those of PBL. The cytotoxicities of rIL-2 activated lymphocytes seemed lower in well differentiated pulmonary adenocarcinoma than in moderately and poorly differentiated adenocarcinoma, and higher in patients with lymph node metastasis than in those without; they appeared, however, not to be related to clinical stage or degree of infiltration of T-zone histiocytes into the cancer stroma. The cytotoxicity to autologous tumor cells was not significantly different in the presence of the Ia antigen expressed on tumor cells, but the cytotoxicity to Ia positive PC-9 cells was significantly higher for rIL-2 activated lymphocytes from patients with lung cancer cells which were Ia positive than from those where they were Ia negative. The presence of Ia antigen on tumor cells seemed important for antitumor activity.
研究了外周血淋巴细胞(PBL)和经体外与重组白细胞介素-2(rIL-2)孵育产生的区域淋巴结淋巴细胞(LNL)的细胞毒性活性,以评估它们对21例肺癌患者自体肺腺癌细胞的作用。PBL对自体肺腺癌细胞的淋巴因子激活的杀伤(LAK)活性为22.9±14.8%,对PC-9细胞的LAK活性为44.9±20%。自体肿瘤细胞与PBL的预共培养(ATS-LAK)对自体肿瘤细胞的细胞毒性诱导未显示增加。LNL的LAK活性明显低于PBL。rIL-2激活的淋巴细胞对高分化肺腺癌的细胞毒性似乎低于中分化和低分化腺癌,对有淋巴结转移患者的细胞毒性高于无淋巴结转移患者;然而,它们似乎与临床分期或T区组织细胞浸润癌基质的程度无关。在肿瘤细胞表达Ia抗原的情况下,对自体肿瘤细胞的细胞毒性无显著差异,但来自Ia阳性肺癌细胞患者的rIL-2激活淋巴细胞对Ia阳性PC-9细胞的细胞毒性明显高于来自Ia阴性患者的淋巴细胞。肿瘤细胞上Ia抗原的存在似乎对抗肿瘤活性很重要。