Accelerated mass production of influenza virus seed stocks in HEK-293 suspension cell cultures by reverse genetics.
Identifieur interne : 000745 ( Main/Exploration ); précédent : 000744; suivant : 000746Accelerated mass production of influenza virus seed stocks in HEK-293 suspension cell cultures by reverse genetics.
Auteurs : Ernest Milián [Canada] ; Thomas Julien [France] ; Rafael Biaggio [Canada] ; Alina Venereo-Sanchez [Canada] ; Johnny Montes [Canada] ; Aziza P. Manceur [Canada] ; Sven Ansorge [Canada] ; Emma Petiot [France] ; Manuel Rosa-Calatrava [France] ; Amine Kamen [Canada]Source :
- Vaccine [ 1873-2518 ] ; 2017.
Descripteurs français
- KwdFr :
- MESH :
- croissance et développement : Sous-type H1N1 du virus de la grippe A, Virus recombinants.
- virologie : Cellules HEK293.
- Bioréacteurs, Culture virale, Génétique inverse, Humains, Tests d'inhibition de l'hémagglutination, Transfection, Vaccins antigrippaux.
English descriptors
- KwdEn :
- MESH :
- chemical : Influenza Vaccines.
- growth & development : Influenza A Virus, H1N1 Subtype, Reassortant Viruses.
- virology : HEK293 Cells.
- Bioreactors, Hemagglutination Inhibition Tests, Humans, Reverse Genetics, Transfection, Virus Cultivation.
- mix :
- Bioreactors, Candidate Vaccine Virus (CVV), H1N1 Subtype, HEK293 Cells, Hemagglutination Inhibition Tests, Humans, Influenza A Virus, Influenza Vaccines, Influenza virus, Large-scale, Pandemic, Reassortant Viruses, Reverse Genetics, Suspension cell culture, Transfection, Transient transfection, Vaccines, Virus Cultivation.
Abstract
Despite major advances in developing capacities and alternative technologies to egg-based production of influenza vaccines, responsiveness to an influenza pandemic threat is limited by the time it takes to generate a Candidate Vaccine Virus (CVV) as reported by the 2015 WHO Informal Consultation report titled "Influenza Vaccine Response during the Start of a Pandemic". In previous work, we have shown that HEK-293 cell culture in suspension and serum free medium is an efficient production platform for cell culture manufacturing of influenza candidate vaccines. This report, took advantage of, recombinant DNA technology using Reverse Genetics of influenza strains, and advances in the large-scale transfection of suspension cultured HEK-293 cells. We demonstrate the efficient generation of H1N1 with the PR8 backbone reassortant under controlled bioreactor conditions in two sequential steps (transfection/rescue and infection/production). This approach could deliver a CVV for influenza vaccine manufacturing within two-weeks, starting from HA and NA pandemic sequences. Furthermore, the scalability of the transfection technology combined with the HEK-293 platform has been extensively demonstrated at >100L scale for several biologics, including recombinant viruses. Thus, this innovative approach is better suited to rationally engineer and mass produce influenza CVV within significantly shorter timelines to enable an effective global response in pandemic situations.
Url:
DOI: 10.1016/j.vaccine.2017.04.065
PubMed: 28495315
Affiliations:
- Canada, France
- Auvergne-Rhône-Alpes, Québec, Rhône-Alpes
- Lyon, Montréal
- Université Claude Bernard Lyon 1, Université McGill
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000418
- to stream PubMed, to step Curation: 000418
- to stream PubMed, to step Checkpoint: 000439
- to stream Ncbi, to step Merge: 001C69
- to stream Ncbi, to step Curation: 001C69
- to stream Ncbi, to step Checkpoint: 001C69
- to stream Hal, to step Corpus: 000036
- to stream Hal, to step Curation: 000036
- to stream Hal, to step Checkpoint: 000295
- to stream Main, to step Merge: 000747
- to stream Main, to step Curation: 000745
Le document en format XML
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<front><div type="abstract" xml:lang="en">Despite major advances in developing capacities and alternative technologies to egg-based production of influenza vaccines, responsiveness to an influenza pandemic threat is limited by the time it takes to generate a Candidate Vaccine Virus (CVV) as reported by the 2015 WHO Informal Consultation report titled "Influenza Vaccine Response during the Start of a Pandemic". In previous work, we have shown that HEK-293 cell culture in suspension and serum free medium is an efficient production platform for cell culture manufacturing of influenza candidate vaccines. This report, took advantage of, recombinant DNA technology using Reverse Genetics of influenza strains, and advances in the large-scale transfection of suspension cultured HEK-293 cells. We demonstrate the efficient generation of H1N1 with the PR8 backbone reassortant under controlled bioreactor conditions in two sequential steps (transfection/rescue and infection/production). This approach could deliver a CVV for influenza vaccine manufacturing within two-weeks, starting from HA and NA pandemic sequences. Furthermore, the scalability of the transfection technology combined with the HEK-293 platform has been extensively demonstrated at >100L scale for several biologics, including recombinant viruses. Thus, this innovative approach is better suited to rationally engineer and mass produce influenza CVV within significantly shorter timelines to enable an effective global response in pandemic situations.</div>
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<tree><country name="Canada"><region name="Québec"><name sortKey="Milian, Ernest" sort="Milian, Ernest" uniqKey="Milian E" first="Ernest" last="Milián">Ernest Milián</name>
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<name sortKey="Ansorge, Sven" sort="Ansorge, Sven" uniqKey="Ansorge S" first="Sven" last="Ansorge">Sven Ansorge</name>
<name sortKey="Biaggio, Rafael" sort="Biaggio, Rafael" uniqKey="Biaggio R" first="Rafael" last="Biaggio">Rafael Biaggio</name>
<name sortKey="Kamen, Amine" sort="Kamen, Amine" uniqKey="Kamen A" first="Amine" last="Kamen">Amine Kamen</name>
<name sortKey="Manceur, Aziza P" sort="Manceur, Aziza P" uniqKey="Manceur A" first="Aziza P" last="Manceur">Aziza P. Manceur</name>
<name sortKey="Montes, Johnny" sort="Montes, Johnny" uniqKey="Montes J" first="Johnny" last="Montes">Johnny Montes</name>
<name sortKey="Venereo Sanchez, Alina" sort="Venereo Sanchez, Alina" uniqKey="Venereo Sanchez A" first="Alina" last="Venereo-Sanchez">Alina Venereo-Sanchez</name>
</country>
<country name="France"><region name="Auvergne-Rhône-Alpes"><name sortKey="Julien, Thomas" sort="Julien, Thomas" uniqKey="Julien T" first="Thomas" last="Julien">Thomas Julien</name>
</region>
<name sortKey="Petiot, Emma" sort="Petiot, Emma" uniqKey="Petiot E" first="Emma" last="Petiot">Emma Petiot</name>
<name sortKey="Rosa Calatrava, Manuel" sort="Rosa Calatrava, Manuel" uniqKey="Rosa Calatrava M" first="Manuel" last="Rosa-Calatrava">Manuel Rosa-Calatrava</name>
</country>
</tree>
</affiliations>
</record>
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