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Production of a novel influenza vaccine using insect cells: protection against drifted strains

A recombinant trivalent hemagglutinin (HA) vaccine produced in cell culture using the baculovirus expression system provides an attractive alternative to the current egg‐based influenza vaccine (Trivalent Inactivated Influenza Vaccine [TIV]) manufacturing process. The HA genes from the annual World...

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Detalles Bibliográficos
Autores principales: Cox, Manon M. J., Karl Anderson, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634664/
https://www.ncbi.nlm.nih.gov/pubmed/19453478
http://dx.doi.org/10.1111/j.1750-2659.2006.00007.x
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author Cox, Manon M. J.
Karl Anderson, D.
author_facet Cox, Manon M. J.
Karl Anderson, D.
author_sort Cox, Manon M. J.
collection PubMed
description A recombinant trivalent hemagglutinin (HA) vaccine produced in cell culture using the baculovirus expression system provides an attractive alternative to the current egg‐based influenza vaccine (Trivalent Inactivated Influenza Vaccine [TIV]) manufacturing process. The HA genes from the annual World Health Organization‐recommended strains are cloned, expressed, and purified using a general purification process. Here, we provide an overview of the expression technology used to make the annual adjustment of the vaccine and the clinical studies completed to date with recombinant HA. The highly purified protein vaccine, administered at three times higher antigen content than TIV, results in stronger immunogenicity, a long‐lasting immune response and provides cross‐protection against drift variant influenza viruses. Furthermore, the vaccine does not contain egg proteins, adjuvants, preservatives, endotoxins, or antibiotics and can therefore be used in a broader population.
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spelling pubmed-46346642015-11-20 Production of a novel influenza vaccine using insect cells: protection against drifted strains Cox, Manon M. J. Karl Anderson, D. Influenza Other Respir Viruses Review Articles A recombinant trivalent hemagglutinin (HA) vaccine produced in cell culture using the baculovirus expression system provides an attractive alternative to the current egg‐based influenza vaccine (Trivalent Inactivated Influenza Vaccine [TIV]) manufacturing process. The HA genes from the annual World Health Organization‐recommended strains are cloned, expressed, and purified using a general purification process. Here, we provide an overview of the expression technology used to make the annual adjustment of the vaccine and the clinical studies completed to date with recombinant HA. The highly purified protein vaccine, administered at three times higher antigen content than TIV, results in stronger immunogenicity, a long‐lasting immune response and provides cross‐protection against drift variant influenza viruses. Furthermore, the vaccine does not contain egg proteins, adjuvants, preservatives, endotoxins, or antibiotics and can therefore be used in a broader population. Blackwell Publishing Ltd 2007-01-19 2007-01 /pmc/articles/PMC4634664/ /pubmed/19453478 http://dx.doi.org/10.1111/j.1750-2659.2006.00007.x Text en
spellingShingle Review Articles
Cox, Manon M. J.
Karl Anderson, D.
Production of a novel influenza vaccine using insect cells: protection against drifted strains
title Production of a novel influenza vaccine using insect cells: protection against drifted strains
title_full Production of a novel influenza vaccine using insect cells: protection against drifted strains
title_fullStr Production of a novel influenza vaccine using insect cells: protection against drifted strains
title_full_unstemmed Production of a novel influenza vaccine using insect cells: protection against drifted strains
title_short Production of a novel influenza vaccine using insect cells: protection against drifted strains
title_sort production of a novel influenza vaccine using insect cells: protection against drifted strains
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634664/
https://www.ncbi.nlm.nih.gov/pubmed/19453478
http://dx.doi.org/10.1111/j.1750-2659.2006.00007.x
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