Desai S A, Maniar H S, Rao R S, Fakih A R, Gangal S G
Immunology Division, Cancer Research Institute, Bombay, India.
Eur J Cancer B Oral Oncol. 1993 Jan;29B(1):69-73. doi: 10.1016/0964-1955(93)90013-5.
Cells from solid tumours are generally poor targets for natural killer (NK) cytotoxicity and antibody dependent cellular cytotoxicity (ADCC). In this paper, we have analysed NK cytotoxicity and ADCC mediated by peripheral blood mononuclear cells from healthy individuals and oral cancer patients before and after modulation with recombinant interleukin-2 (rIL-2), on target cells derived from two squamous cell carcinoma (SCC) cell lines prior to and after treatment with recombinant interferon-alpha (rIFN alpha). Target SCC cell directed monoclonal antibody 3F8E3 was used in ADCC. The results showed that the unmodulated SCC cells were poor targets for NK and ADCC compared to standard targets (K562 cells and chicken red blood cells, respectively). Modulation of targets alone with rIFN alpha showed moderate increase in their susceptibility while rIL-2 treated effectors could significantly lyse even unmodulated targets. Combined treatment of targets with rIFN alpha and effectors with rIL-2 showed additive enhancement in NK and ADCC activity against SCC cells. Lymphocytes from treated patients with recurrent disease could not efficiently lyse SCC targets even after combined modulation.
实体瘤细胞通常是自然杀伤(NK)细胞毒性和抗体依赖性细胞毒性(ADCC)的较差靶标。在本文中,我们分析了健康个体和口腔癌患者外周血单个核细胞在经重组白细胞介素-2(rIL-2)调节前后,对来自两种鳞状细胞癌(SCC)细胞系的靶细胞在重组干扰素-α(rIFNα)处理前后的NK细胞毒性和ADCC。在ADCC中使用了针对靶SCC细胞的单克隆抗体3F8E3。结果表明,与标准靶标(分别为K562细胞和鸡红细胞)相比,未调节的SCC细胞是NK细胞毒性和ADCC的较差靶标。单独用rIFNα调节靶标显示其敏感性有适度增加,而经rIL-2处理的效应细胞甚至可以显著裂解未调节的靶标。用rIFNα处理靶标和用rIL-2处理效应细胞的联合处理显示对SCC细胞的NK细胞毒性和ADCC活性有累加增强作用。患有复发性疾病的经治疗患者的淋巴细胞即使在联合调节后也不能有效裂解SCC靶标。