Cytokine gene transduction in tumor cells: interleukin (IL)-2 or IL-4 gene transfer in human melanoma cells.

Natural immunity Pub Date : 1994-03-01
C Melani, C Chiodoni, F Arienti, C Maccalli, J Sule-Suso, A Anichini, M P Colombo, G Parmiani
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Abstract

Cytokine gene transfer into mouse tumor cells has been shown to stimulate a strong immune response resulting in the rejection of the transduced tumor when injected in vivo. Therefore, retroviral vectors containing the human interleukin (IL)-2 or IL-4 gene have been constructed to transduce human melanoma cells to explore whether their immunogenicity can be increased both in vitro and in vivo. Our preliminary results indicate that retroviral vectors can efficiently transduce the IL-2 and or IL-4 gene into melanoma clones, inducing production of either cytokine in the range of 0.5-2 ng/ml/10(5) cells in 48-72 h. No modifications of the growth rate, morphology and antigenicity of the transduced tumor cells were found.

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肿瘤细胞中的细胞因子基因转导:白细胞介素(IL)-2或IL-4基因在人类黑色素瘤细胞中的转移。
细胞因子基因转移到小鼠肿瘤细胞中已被证明在体内注射时可刺激强烈的免疫反应,导致对转导肿瘤的排斥反应。因此,我们构建了含有人白细胞介素(IL)-2或IL-4基因的逆转录病毒载体来转导人黑色素瘤细胞,以探索是否可以在体外和体内提高其免疫原性。我们的初步结果表明,逆转录病毒载体可以有效地将IL-2和/或IL-4基因转导到黑色素瘤克隆中,诱导在48-72小时内产生0.5-2 ng/ml/10(5)个细胞的细胞因子。转导后的肿瘤细胞的生长速度、形态和抗原性没有改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Author Index Vol. 16, 1998 Subject Index Vol. 16, 1998 Contents Vol. 16, 1998 Preliminary Pages Session I: Ontogeny and Differentiation of NK and NK-Like Cells
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