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流感病毒样颗粒生物工艺的进展。

Advances in influenza virus-like particles bioprocesses.

机构信息

Virologie et Pathologie Humaine - VirPath team - Centre International de Recherche en Infectiologie (CIRI), INSERM U1111, CNRS UMR5308, ENS Lyon, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.

VirNext, Faculté de Médecine RTH Laennec, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.

出版信息

Expert Rev Vaccines. 2019 Dec;18(12):1285-1300. doi: 10.1080/14760584.2019.1704262.

DOI:10.1080/14760584.2019.1704262
PMID:31829068
Abstract

: Influenza Virus-like Particles (VLPs) are one of the most promising vaccine strategies to complement traditional egg-based processes and contribute to shortening the response time when facing future pandemics. Research programs have taken advantage of the potential of this approach to produce influenza VLPs on a variety of cellular platforms, reaching the industrial level of development and recent commercialization.: This review aims to give an overview of available strategies for influenza-VLP production and their respective stages of development, from small-scale preclinical studies to large-scale industrial processes. Recent trends and fulfillments in purification schemes of influenza VLP were also reviewed with regards to quality and potency requirements that go along with influenza vaccine manufacturing.: In the next five years, it is expected that there will be licensing of new influenza vaccine products based on VLP strategy. Few VLP upstream processes are mature enough and close to fully complement or seriously concurrence the ovoculture process. Nevertheless, many improvements have yet to be achieved in downstream processes. In the next few years, research efforts in this field are expected to provide purification strategies and tools to achieve higher recovery yields and improve the cost-effectiveness of VLP processes.

摘要

流感病毒样颗粒(VLPs)是最有前途的疫苗策略之一,可以补充传统的基于鸡蛋的工艺,并有助于缩短未来大流行时的应对时间。研究计划利用这种方法的潜力,在各种细胞平台上生产流感 VLPs,达到了工业发展水平,并实现了最近的商业化。

本综述旨在概述流感-VLP 生产的可用策略及其各自的开发阶段,从小规模临床前研究到大规模工业生产。还回顾了流感 VLP 纯化方案的最新趋势和进展,以及与流感疫苗生产相关的质量和效力要求。

在未来五年内,预计将有基于 VLP 策略的新流感疫苗产品获得许可。少数 VLP 上游工艺已经足够成熟,接近于完全补充或严重竞争卵培养工艺。然而,下游工艺仍有许多改进之处。在未来几年,预计该领域的研究工作将提供纯化策略和工具,以提高回收率和提高 VLP 工艺的成本效益。

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