Analytical technologies for influenza virus-like particle candidate vaccines: Challenges and emerging approaches

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DOITrouver le DOI : http://doi.org/10.1186/1743-422X-10-141
AuteurRechercher : ; Rechercher : ; Rechercher : ; Rechercher : ; Rechercher :
TypeArticle
Titre de la revueVirology Journal
ISSN1743-422X
Volume10
Numéro d'article141
Sujetinfluenza vaccine; influenza virus like particle vaccine; unclassified drug; virus protein; cell strain HEK293; DNA vector; electron microscopy; enzyme activity; enzyme linked immunosorbent assay; HeLa cell; immunodiffusion; Influenza virus; insect cell; protein analysis; reversed phase high performance liquid chromatography; review; Vero cell; virion; virus hemagglutination; virus strain; Western blotting; Orthomyxoviridae
RésuméInfluenza virus-like particle vaccines are one of the most promising ways to respond to the threat of future influenza pandemics. VLPs are composed of viral antigens but lack nucleic acids making them non-infectious which limit the risk of recombination with wild-type strains. By taking advantage of the advancements in cell culture technologies, the process from strain identification to manufacturing has the potential to be completed rapidly and easily at large scales. After closely reviewing the current research done on influenza VLPs, it is evident that the development of quantification methods has been consistently overlooked. VLP quantification at all stages of the production process has been left to rely on current influenza quantification methods (i.e. Hemagglutination assay (HA), Single Radial Immunodiffusion assay (SRID), NA enzymatic activity assays, Western blot, Electron Microscopy). These are analytical methods developed decades ago for influenza virions and final bulk influenza vaccines. Although these methods are time-consuming and cumbersome they have been sufficient for the characterization of final purified material. Nevertheless, these analytical methods are impractical for in-line process monitoring because VLP concentration in crude samples generally falls out of the range of detection for these methods. This consequently impedes the development of robust influenza-VLP production and purification processes. Thus, development of functional process analytical techniques, applicable at every stage during production, that are compatible with different production platforms is in great need to assess, optimize and exploit the full potential of novel manufacturing platforms. © 2013 Thompson et al.; licensee BioMed Central Ltd.
Date de publication
Langueanglais
AffiliationConseil national de recherches Canada (CNRC-NRC); Thérapeutiques en santé humaine (TSH-HHT)
Publications évaluées par des pairsOui
Numéro NPARC21269975
Exporter la noticeExport en format RIS
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Identificateur de l’enregistrementc21848bf-d808-44a0-a341-ec9e862aad69
Enregistrement créé2013-12-13
Enregistrement modifié2016-05-09
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