tetano
Editor, Senior Moderator
Expert Rev Vaccines. 2019 Dec 12. doi: 10.1080/14760584.2019.1704262. [Epub ahead of print] [h=1]Advances in Influenza Virus-Like Particles bioprocesses.[/h]
Durous L[SUP]1[/SUP], Rosa-Calatrava M[SUP]1,[/SUP][SUP]2[/SUP], Petiot E[SUP]1[/SUP].
[h=3]Author information[/h] 1 Virologie et Pathologie Humaine - VirPath teamCentre International de Recherche en Infectiologie (CIRI), INSERM U1111, CNRS UMR5308, ENS Lyon, Universit? Claude Bernard Lyon 1, Universit? de Lyon, Lyon 69008, France. 2 VirNext, Facult? de M?decine RTH Laennec, Universit? Claude Bernard Lyon 1, Universit? de Lyon, Lyon 69008, France.
[h=3]Abstract[/h] 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 industrial level of development and recent commercialization.Area Covered:This review aims to give an overview of available strategies for influenza VLP production and their respective stage 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.Expert opinion: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 and close to 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.
[h=4]KEYWORDS:[/h] Downstream Process (DSP); Influenza Virus-like Particles; Recombinant vaccine; Upstream Process (USP)
PMID: 31829068 DOI: 10.1080/14760584.2019.1704262
Durous L[SUP]1[/SUP], Rosa-Calatrava M[SUP]1,[/SUP][SUP]2[/SUP], Petiot E[SUP]1[/SUP].
[h=3]Author information[/h] 1 Virologie et Pathologie Humaine - VirPath teamCentre International de Recherche en Infectiologie (CIRI), INSERM U1111, CNRS UMR5308, ENS Lyon, Universit? Claude Bernard Lyon 1, Universit? de Lyon, Lyon 69008, France. 2 VirNext, Facult? de M?decine RTH Laennec, Universit? Claude Bernard Lyon 1, Universit? de Lyon, Lyon 69008, France.
[h=3]Abstract[/h] 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 industrial level of development and recent commercialization.Area Covered:This review aims to give an overview of available strategies for influenza VLP production and their respective stage 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.Expert opinion: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 and close to 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.
[h=4]KEYWORDS:[/h] Downstream Process (DSP); Influenza Virus-like Particles; Recombinant vaccine; Upstream Process (USP)
PMID: 31829068 DOI: 10.1080/14760584.2019.1704262