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致癌性逆转录病毒和慢病毒基因治疗载体的下游处理

Downstream processing of oncoretroviral and lentiviral gene therapy vectors.

作者信息

Segura María de Las Mercedes, Kamen Amine, Garnier Alain

机构信息

Department of Chemical Engineering, Centre de Recherche sur la fonction, la structure et l'ingénierie des protéines, Université Laval, Québec, Canada G1K 7P4.

出版信息

Biotechnol Adv. 2006 May-Jun;24(3):321-37. doi: 10.1016/j.biotechadv.2005.12.001. Epub 2006 Jan 30.

Abstract

Retroviral vectors from both oncoretroviral and lentiviral origins have a great potential as gene delivery vehicles. A number of research groups have devoted considerable effort to the development of large-scale production strategies for retroviral vectors. However, the manufacturing of clinical-grade vectors for gene therapy, especially for in vivo applications, additionally requires scaleable purification strategies to remove the contaminants present in the harvested supernatants while preserving the functionality of the vectors. In this article, we review recent advances made in the field of downstream processing of retroviral vectors. The methods currently described in the literature for clarification, concentration and purification of retroviral vectors will be presented, with special emphasis on novel chromatography methods that open up the possibility to selectively and efficiently purify retroviruses on a large-scale. Problems associated with stability and quantification of retroviral particles will be outlined and future challenges will be discussed.

摘要

源自嗜肝DNA病毒逆转录病毒和慢病毒的逆转录病毒载体作为基因传递载体具有巨大潜力。许多研究小组在开发逆转录病毒载体的大规模生产策略方面投入了大量精力。然而,用于基因治疗的临床级载体的生产,尤其是体内应用,还需要可扩展的纯化策略,以去除收获的上清液中存在的污染物,同时保留载体的功能。在本文中,我们综述了逆转录病毒载体下游加工领域的最新进展。将介绍目前文献中描述的用于逆转录病毒载体澄清、浓缩和纯化的方法,特别强调新型色谱方法,这些方法为大规模选择性和高效纯化逆转录病毒开辟了可能性。将概述与逆转录病毒颗粒稳定性和定量相关的问题,并讨论未来的挑战。

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