细胞因子对肿瘤细胞特异性和非特异性细胞毒性的不同影响。

H Naganuma, E Halapi, G Masucci, M Hansson, P Wersäll, C Hising, S Venkateswaran, H Mellstedt, R Kiessling
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引用次数: 2

摘要

分析了ifn - γ和tnf - α对卵巢癌细胞系特异性CTL克隆和从腹水分离的非特异性肿瘤相关淋巴细胞(TAL)裂解敏感性的影响。体外建立的TAL细胞系对自体肿瘤和几种异体肿瘤均表现出非特异性的裂解活性。单独使用ifn - γ或与tnf - α联合进行预处理,使癌细胞不容易被自体TAL细胞系溶解。相反,从TAL细胞系中分离出来的肿瘤特异性T细胞克隆对裂解的敏感性由于细胞因子预处理而增加。几个tcr - α / β +, CD8+ t细胞克隆对自体肿瘤表现出更特异性的裂解模式。根据抗体阻断研究推断,这些克隆通过依赖于粘附分子ICAM-1和LFA-3的mhc类I限制性机制裂解自体肿瘤涉及tcr - α / β。细胞因子处理后卵巢癌细胞对特异性CTL克隆的敏感性增强可能与ICAM-1分子在卵巢癌细胞上的表达增强有关。这些结果对基于细胞因子的免疫治疗具有启示意义,其中ifn - γ可能增强肿瘤相关特异性CTL的作用,同时降低非特异性效应细胞的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diverse effect of cytokine treatment of tumor cells on specific versus non-specific cytotoxicity.

The effect of IFN-gamma and TNF-alpha treatment of an ovarian carcinoma line on the sensitivity to lysis by specific CTL clones and non-specific Tumor Associated Lymphocytes (TAL), isolated from the ascites fluid, was analyzed. The in vitro established TAL line displayed a non-specific lytic activity against the autologous tumor as well as against several allogeneic tumor lines. Pretreatment with IFN-gamma alone, or in combination with TNF-alpha, rendered the carcinoma line less susceptible to lysis by the autologous TAL line. Conversely, susceptibility to lysis by tumor specific T cell clones, isolated from the TAL line, was increased as a result of cytokine pretreatment. Several TCR-alpha/beta+, CD8+ T-cell clones showing a more specific pattern of lysis against the autologous tumor were isolated. Lysis of the autologous tumor by these clones involved the TCR-alpha/beta via a MHC-class I restricted mechanism dependent on the adhesion molecules ICAM-1 and LFA-3, as inferred from antibody blocking studies. The enhanced sensitivity to specific CTL clones seen after cytokine treatment may be related to the enhanced expression of ICAM-1 molecules on the ovarian carcinoma. These results have implications for cytokine based immunotherapy, where IFN-gamma may enhance the effects of tumor associated specific CTL while decreasing that of non-specific effector cells.

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