获得由重组腺病毒转导的细胞系产生的重组抗体的方法

E. Sedova, D. N. Shcherbinin, A. S. Bandelyuk, L. V. Verkhovskaya, N. Viskova, E. D. Avdonina, V. V. Prokofiev, E. I. Ryabova, I. Esmagambetov, K. A. Pervoykina, E. Bogacheva, A. Lysenko, M. Shmarov
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摘要

目标。以两种广谱抗流感抗体27F3和cr9114为例,利用携带重链和轻链抗体基因的重组腺病毒血清型5 (rAd5)转导人HEK293细胞悬浮培养获得重组抗体的技术。Ad5-27F3-H、ad5 - cr914 - h和Ad5-27F3-L重组腺病毒分别携带27F3抗体重链基因、CR9114抗体重链基因和27F3轻链基因,采用AdEasy™腺病毒载体系统制备。为了积累制备量的重组r27F3和rCR9114抗体,用携带抗体重链和轻链基因的重组腺病毒转导HEK293悬浮细胞系。细胞在波浪型生物反应器中培养。用层析法从培养基中纯化重组抗体。用蛋白电泳分析纯化抗体的分子量后,用Western blot技术分析其与甲型流感病毒和乙型流感病毒的相互作用能力,并用病毒中和试验评价其中和甲型流感病毒和乙型流感病毒的能力。本研究建立了一种从人细胞悬浮培养培养基中积累和纯化重组r27F3和CR9114抗体的方法,该方法通过转染重组腺病毒获得重组r27F3和CR9114抗体的重链和轻链基因。r27F3抗体能够与甲型流感病毒1组(除甲型流感病毒亚型H2外)和甲型流感病毒2组相互作用和中和。结果表明,rCR9114抗体能与甲型流感病毒和乙型流感病毒相互作用,并能中和甲型流感病毒。在HEK293细胞悬浮培养中,利用携带表达重链和轻链抗体基因的重组腺病毒转导获得重组抗体的技术得到了发展,并证实了它们的特异性。
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Method for obtaining recombinant antibodies produced by a cell line transduced with recombinant adenoviruses
Objectives. To develop a technology for obtaining recombinant antibodies in a suspension culture of human HEK293 cells using transduction with recombinant adenovirus serotype 5 (rAd5) carrying genes expressing heavy and light chains of antibodies on the example of two broadspectrum anti-influenza antibodies 27F3 and CR9114.Methods. Ad5-27F3-H, Ad5-CR9114-H, and Ad5-27F3-L recombinant adenoviruses carrying the 27F3 antibody heavy chain gene, CR9114 antibody heavy chain gene, and 27F3 light chain gene, respectively, were generated using the AdEasy™ Adenoviral vector system. To accumulate preparative amounts of recombinant r27F3 and rCR9114 antibodies, the HEK293 suspension cell line was transduced with recombinant adenoviruses carrying genes for heavy and light chains of antibodies. The cells were cultured in a wave-type bioreactor. Chromatography was used to purify recombinant antibodies from the culture medium. After analyzing the molecular weights of purified antibodies using protein electrophoresis, their ability to interact with influenza A and B viruses was analyzed using the Western blot technique, while their ability to neutralize influenza A and B viruses was evaluated using the virus neutralization assay.Results. A method for the accumulation and purification of recombinant r27F3 and CR9114 antibodies from the culture medium of a suspension culture of human cells following transduction with its recombinant adenoviruses carrying the genes for heavy and light chains of these antibodies was developed. The ability of the r27F3 antibody to interact with and neutralize influenza A viruses of group 1 (except influenza A virus subtype H2) and group 2 was shown. The ability of the rCR9114 antibody to interact with influenza A viruses of group 1 and influenza B viruses, as well as to neutralize influenza A viruses of group 1, was demonstrated.Conclusions. A technology for obtaining recombinant antibodies in a suspension culture of HEK293 cells using transduction with recombinant adenoviruses carrying genes expressing heavy and light chains of antibodies was developed along with a confirmation of their specificity.
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