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Journal ArticleDOI

Eight-plasmid system for rapid generation of influenza virus vaccines.

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TLDR
These findings demonstrate that the eight-plasmid system allows the rapid and reproducible generation of reassortant influenza A viruses for use in the manufacture of vaccines.
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This article is published in Vaccine.The article was published on 2002-08-19. It has received 443 citations till now. The article focuses on the topics: Influenza A virus & Orthomyxoviridae.

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The Intracellular Sensor NLRP3 Mediates Key Innate and Healing Responses to Influenza A Virus via the Regulation of Caspase-1

TL;DR: It is demonstrated that Nlrp3 and Casp1(-/-) mice were more susceptible than wild-type mice after infection with a pathogenic influenza A virus, and cryopyrin and caspase-1 are central to both innate immunity and to moderating lung pathology in influenza pneumonia.
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Are we ready for pandemic influenza

TL;DR: Here, progress to date in preparedness for an influenza pandemic is considered and what remains to be done is reviewed, with prioritizing the remaining needs and exploring the reasons for the current lack of preparedness.
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Virus glycosylation: role in virulence and immune interactions

TL;DR: This review focuses on recent findings on the importance of glycosylation to viral virulence and immune evasion for several prominent human pathogens.
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Age-associated decline in T cell repertoire diversity leads to holes in the repertoire and impaired immunity to influenza virus

TL;DR: It is shown in a mouse infection model that naturally occurring contraction of the naive T cell repertoire can result in impaired CD8 T cell responses to known immunodominant epitopes and decline in heterosubtypic immunity, which has important implications for the design of vaccine strategies for the elderly.
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Evolution of H5N1 avian influenza viruses in Asia

Jean Thierry Aubin, +93 more
TL;DR: Human infections were from a virus clade undergoing antigenic drift that showed resistance to adamantanes but sensitivity to neuraminidase inhibitors.
References
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Journal ArticleDOI

Universal primer set for the full-length amplification of all influenza A viruses.

TL;DR: The resultant primer set is suitable for all influenza A viruses to generate full-length cDNAs, to subtype viruses, to sequence their DNA, and to construct expression plasmids for reverse genetics systems.
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A DNA transfection system for generation of influenza A virus from eight plasmids

TL;DR: An eight-plasmid DNA transfection system for the rescue of infectious influenza A virus from cloned cDNA facilitates the design and recovery of both recombinant and reassortant influenza A viruses, and may also be applicable to the recovery of other RNA viruses entirely from cloning cDNA.
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Human influenza A H5N1 virus related to a highly pathogenic avian influenza virus

TL;DR: The results suggest transmission of the virus from infected chickens to the child without another intermediate mammalian host acting as a "mixing vessel" illustrates the importance of intensive global influenza surveillance.
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Generation of influenza A viruses entirely from cloned cDNAs

TL;DR: A new reverse-genetics system that allows one to efficiently generate influenza A viruses entirely from cloned cDNAs is described, which should be useful in viral mutagenesis studies and in the production of vaccines and gene therapy vectors.
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