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基于爱泼斯坦-巴尔病毒的附加型载体在人淋巴瘤细胞中表达细胞因子基因的适用性。

Suitability of Epstein-Barr virus-based episomal vectors for expression of cytokine genes in human lymphoma cells.

作者信息

Mũcke S, Polack A, Pawlita M, Zehnpfennig D, Massoudi N, Bohlen H, Doerfler W, Bornkamm G, Diehl V, Wolf J

机构信息

University of Cologne, Department of Internal Medicine I, Munich, Germany.

出版信息

Gene Ther. 1997 Feb;4(2):82-92. doi: 10.1038/sj.gt.3300363.

Abstract

Plasmids carrying the Epstein-Barr virus (EBV) latent gene EBNA1 and the EBV latent origin of replication (oriP) stay in transfected human cells as autonomously replicating extrachromosomal genetic units. They thus might represent a suitable tool for cytokine gene introduction into human tumor cells with the prospect of therapeutic antitumor vaccination. The aim of this study was to analyze whether such plasmids permit stable and efficient expression of cytokine genes in human non-Hodgkin lymphoma cells. We tested physical stability and expression levels of plasmids carrying EBNA1 and oriP for episomal maintenance, immunoglobulin light chain enhancer elements for augmentation of expression, and cytokine or marker genes after introduction into human NHL cell lines in vitro and in vivo after inoculation into nude mice. Data obtained with these EBV-based vectors were compared with another plasmid, not carrying EBNA1 and oriP. cDNAs coding for GM-CSF, IL6, TNF alpha, the chloramphenicolacetyltransferase (CAT) and the beta-galactosidase (lacZ) gene were transfected into the EBV-positive Burkitt's lymphoma cell line BL60 and the EBV-negative B cell lymphoma cell line BJA-B. EBV-derived vectors permitted a high, host cell independent transfection efficiency and high and host cell independent levels of expression. After removal of the selection pressure (hygromycin B) cytokine expression could be detected for several weeks in vitro and in vivo but, however, declined continuously. These experiments suggest that episomal BC-derived vectors represent an effective tool for cytokine gene transfer in human lymphoma cells.

摘要

携带爱泼斯坦-巴尔病毒(EBV)潜伏基因EBNA1和EBV潜伏复制起点(oriP)的质粒作为自主复制的染色体外遗传单位存在于转染的人类细胞中。因此,它们可能是将细胞因子基因导入人类肿瘤细胞的合适工具,有望用于治疗性抗肿瘤疫苗接种。本研究的目的是分析此类质粒是否能使人非霍奇金淋巴瘤细胞稳定、高效地表达细胞因子基因。我们测试了携带EBNA1和oriP用于游离维持的质粒、用于增强表达的免疫球蛋白轻链增强子元件以及在体外导入人NHL细胞系后和接种到裸鼠体内后细胞因子或标记基因的物理稳定性和表达水平。将这些基于EBV的载体获得的数据与另一种不携带EBNA1和oriP的质粒进行比较。将编码GM-CSF、IL6、TNFα、氯霉素乙酰转移酶(CAT)和β-半乳糖苷酶(lacZ)基因的cDNA转染到EBV阳性的伯基特淋巴瘤细胞系BL60和EBV阴性的B细胞淋巴瘤细胞系BJA-B中。EBV衍生的载体允许高的、不依赖宿主细胞的转染效率以及高的、不依赖宿主细胞的表达水平。去除选择压力(潮霉素B)后,在体外和体内都能在数周内检测到细胞因子表达,但会持续下降。这些实验表明,游离的BC衍生载体是将细胞因子基因转移到人类淋巴瘤细胞中的有效工具。

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