Suitability of PER.C6 (R) cells to generate epidemic and pandemic influenza vaccine strains by reverse genetics
Autor: | Jaap Goudsmit, Ronald Vogels, L. Hartgroves, C. Ophorst, Lisette A. H. M. Cornelissen, Isabelle Legastelois, Menzo J. E. Havenga, Wendy S. Barclay, Wouter Koudstaal, David Zuijdgeest, O. S. de Leeuw, Jerome Custers, Martijn Sieuwerts, E.A. de Boer-Luijtze |
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Přispěvatelé: | TNO Kwaliteit van Leven, Other departments |
Jazyk: | angličtina |
Rok vydání: | 2009 |
Předmět: |
Biomedical Research
Influenza vaccine Cell Culture Techniques Viral Plaque Assay Biology dna system medicine.disease_cause Antibodies Viral Transfection Severity of Illness Index Microbiology Cell Line Mice Influenza A Virus H1N1 Subtype CVI - Divisie Virologie establishment Reassortant Viruses Influenza Human medicine Influenza A virus Animals Humans rna-polymerase Virus quantification Plaque Assay Mice Inbred BALB C General Veterinary General Immunology and Microbiology Influenza A Virus H5N1 Subtype Influenza A Virus H3N2 Subtype Public Health Environmental and Occupational Health Hemagglutination Inhibition Tests Virology Survival Analysis Influenza A virus subtype H5N1 Reverse genetics Vaccination Infectious Diseases Influenza Vaccines Inactivated vaccine Molecular Medicine rescue Female a virus generation CVI - Division Virology |
Zdroj: | Vaccine 27 (2009) 19 Vaccine, 27(19), 2588-2593 Vaccine, 27(19), 2588-2593. Elsevier BV Vaccine, 19, 27, 2588-2593 |
ISSN: | 0264-410X |
Popis: | Reverse genetics, the generation of influenza viruses from cDNA, presents a rapid method for creating vaccine strains. The technique necessitates the use of cultured cells. Due to technical and regulatory requirements, the choice of cell lines for production of human influenza vaccines is limited. PER.C6® cells, among the most extensively characterized and documented cells, support growth of all influenza viruses tested to date, and can be grown to high densities in large bioreactors in the absence of serum or micro carriers. Here, the suitability of these cells for the generation of influenza viruses by reverse genetics was investigated. A range of viruses reflective of vaccine strains was rescued exclusively using PER.C6 cells by various transfection methods, including an animal component-free procedure. Furthermore, a whole inactivated vaccine carrying the HA and NA segments of A/HK/156/97 (H5N1) that was both rescued from and propagated on PER.C6 cells, conferred protection in a mouse model. Thus PER.C6 cells provide an attractive platform for generation of influenza vaccine strains via reverse genetics. © 2009 Elsevier Ltd. All rights reserved. |
Databáze: | OpenAIRE |
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