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Cell Culture Processes for the Production of Viral Vectors for Gene Therapy Purposes

机译:细胞培养过程用于基因治疗目的的病毒载体的生产

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摘要

Gene therapy is a promising technology for the treatment of several acquired and inherited diseases. However, for gene therapy to be a commercial and clinical success, scalable cell culture processes must be in place to produce the required amount of viral vectors to meet market demand. Each type of vector has its own distinct characteristics and consequently its own challenges for production. This article reviews the current technology that has been developed for the efficient, large-scale manufacture of retrovirus, lentivirus, adenovirus, adeno-associated virus and herpes simplex virus vectors.
机译:基因疗法是一种用于治疗多种获得性和遗传性疾病的有前途的技术。然而,为了使基因疗法在商业上和临床上取得成功,必须采用可扩展的细胞培养方法以产生所需量的病毒载体以满足市场需求。每种类型的载体都有其独特的特性,因此也具有生产上的挑战。本文介绍了为高效,大规模生产逆转录病毒,慢病毒,腺病毒,腺相关病毒和单纯疱疹病毒载体而开发的当前技术。

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