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Structure and expression of integrated hepatitis B virus genes in an HBs antigen producing human cell line (huGK-14)

机译:合成乙型肝炎病毒基因在产生HBs抗原的人类细胞系(huGK-14)中的结构和表达

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摘要

A human continuous cell line (huGK-14) within a lineage of passaged cultures was investigated in the mode of integration and expression of hepatitis B virus (HBV) genes. HBV DNA was integrated in eight different sites of the cellular DNA, in each of which HBV genome was rearranged, fragmented, and/or partly deleted. Complete HBV genome that may lead to production of infectious virus particles was not detected in the cells nor in the culture medium. Clones of cDNA containing a complete coding frame for small HBs antigen protein (type adr) were obtained from mRNA of the cells. The cells were stable over the period of six months of cultivation and more than 60 population doublings in the mode of HBV integration and HBs mRNA expression.These results provide substantial evidence for the absence of an ability for the integrated DNA to create an infectious product in the cell; for the stable production of HBs mRNA from the cells, and suggest the usefulness of this cell line as a substrate for HBV vaccine production.
机译:以乙型肝炎病毒(HBV)基因的整合和表达模式研究了传代培养谱系中的人类连续细胞系(huGK-14)。 HBV DNA被整合到细胞DNA的八个不同位点,在每个位点中,HBV基因组都被重新排列,片段化和/或部分缺失。在细胞或培养基中均未检测到可能导致感染性病毒颗粒产生的完整HBV基因组。从细胞的mRNA中获得了含有完整的小HBs抗原蛋白(adr型)编码框架的cDNA克隆。这些细胞在六个月的培养过程中保持稳定,并以HBV整合和HBs mRNA表达的方式增加了60倍以上的种群数量,这些结果为整合的DNA缺乏创造传染性产物的能力提供了充分的证据。细胞;从细胞中稳定产生HBs mRNA的证据,并暗示该细胞系可用作HBV疫苗生产的底物。

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