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Universal Vaccines and Vaccine Platforms to Protect against Influenza Viruses in Humans and Agriculture.

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TLDR
Current vaccines to protect humans and animals against influenza are discussed, highlighting challenges faced to effective and uniform novel vaccination strategies and approaches.
Abstract
Influenza virus infections pose a significant threat to public health due to annual seasonal epidemics and occasional pandemics. Influenza is also associated with significant economic losses in animal production. The most effective way to prevent influenza infections is through vaccination. Current vaccine programs rely heavily on the vaccine's ability to stimulate neutralizing antibody responses to the hemagglutinin (HA) protein. One of the biggest challenges to an effective vaccination program lies on the fact that influenza viruses are ever-changing, leading to antigenic drift that results in escape from earlier immune responses. Efforts toward overcoming these challenges aim at improving the strength and/or breadth of the immune response. Novel vaccine technologies, the so-called universal vaccines, focus on stimulating better cross-protection against many or all influenza strains. However, vaccine platforms or manufacturing technologies being tested to improve vaccine efficacy are heterogeneous between different species and/or either tailored for epidemic or pandemic influenza. Here, we discuss current vaccines to protect humans and animals against influenza, highlighting challenges faced to effective and uniform novel vaccination strategies and approaches.

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Citations
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Mechanism of Virus Attenuation by Codon Pair Deoptimization

TL;DR: It is shown that suboptimal codon pairs cause attenuation, whereas the increase of CpG dinucleotides has no effect, and that codon pair bias can be used to increase mRNA stability and protein production of synthetic genes in many areas of biotechnology.
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Novel Approaches for The Development of Live Attenuated Influenza Vaccines

TL;DR: The discovery and implementation of plasmid-based reverse genetics has been a key advance in the rapid generation of recombinant attenuated influenza viruses that can be used for the development of new and most effective LAIVs, which reveal their possible implementation in combating influenza infections.
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A single dose of a vesicular stomatitis virus-based influenza vaccine confers rapid protection against H5 viruses from different clades

TL;DR: It was found that a single dose of VSV vectors expressing full-length hemagglutinin (HAfl) were sufficient to provide 100% protection, highlighting the potential of the VSV-based HAfl as a pan-H5 influenza virus emergency vaccine.
Journal ArticleDOI

Enhanced inhibition of influenza virus infection by peptide-noble-metal nanoparticle conjugates.

TL;DR: It is demonstrated that conjugation of FluPep to gold and silver nanoparticles enhances its antiviral potency; the antimicrobial activity of silver ions may enable the design of even more potent antimicrobial inhibitors, capable of targeting both influenza and bacterial co-infections.
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Comparing influenza vaccine effectiveness between cell-derived and egg-derived vaccines, 2017-2018 influenza season.

TL;DR: The cell-derived and egg-derived vaccines were moderately protective against all influenza types with significant VE estimates for all dependents at 46% (95% confidence interval, 33, 56) and 53% (45, 60), respectively.
References
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Journal ArticleDOI

T-cell help for cytotoxic T lymphocytes is mediated by CD40–CD40L interactions

TL;DR: In this paper, it was shown that signalling through CD40 can replace CD4+ T-helper cells in priming of helper-dependent CD8+ CTL responses.
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Origins and evolutionary genomics of the 2009 swine-origin H1N1 influenza A epidemic.

TL;DR: It is shown that the new swine-origin influenza A (H1N1) virus emerged in Mexico and the United States was derived from several viruses circulating in swine, and that the initial transmission to humans occurred several months before recognition of the outbreak.
Journal ArticleDOI

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.
Journal ArticleDOI

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.
Journal ArticleDOI

Antibody Recognition of a Highly Conserved Influenza Virus Epitope

TL;DR: TheCR6261 epitope identified here should accelerate the design and implementation of improved vaccines that can elicit CR6261-like antibodies, as well as antibody-based therapies for the treatment of influenza.
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