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J Med Virol . Likelihood of prior exposure to circulating influenza viruses resulting in cross protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans

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  • J Med Virol . Likelihood of prior exposure to circulating influenza viruses resulting in cross protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans


    J Med Virol


    . 2021 Aug 27.
    doi: 10.1002/jmv.27299. Online ahead of print.
    Likelihood of prior exposure to circulating influenza viruses resulting in cross protection by CD8+ T cells against emergent H3N2v swine viruses infecting humans


    Naomi Komadina 1 , Sheena Sullivan 2 , Karin Leder 3 , Jodie McVernon 4



    Affiliations

    Abstract

    Outbreaks of influenza in swine can result in potential threats to human public health. A notable occurrence was the emergence of swine-origin H1N1 influenza viruses in 2009. Since then, there have been several documented outbreaks of swine origin influenza infecting humans in several countries. Sustained events have occurred when H1N1v, H1N2v and H3N2v swine origin viruses have infected humans visiting agricultural shows in the US. The predominant H3N2v viruses gained the matrix protein from the A(H1N1)pdm09 viruses, with reported human-to-human transmission raising fears of another pandemic. Current vaccines do not induce secondary cell-mediated immune responses, which may provide cross-protection against novel influenza A subtypes, however population susceptibility to infection with seasonal influenza is likely to be influenced by cross-reactive CD8+T-cells directed towards immunogenic peptides derived from viral proteins. This study involved a retrospective review of historical influenza viruses circulating in human populations from 1918 to 2020 to identify evidence of prior circulation of H3N3v immunogenic CD8+T-cells peptides found in the NP and M1 proteins. We found evidence of prior circulation of H3N2v NP and M1 immunogenic peptides in historical influenza viruses. This provides insight into the population context in which influenza viruses emerge and may help inform immunogenic peptide selection for Cytotoxic T-cell Lymphocytes (CTL)-inducing influenza vaccines. Next generation vaccines capable of eliciting CD8+T-cell mediated cross-protective immunity may offer a long-term alternative strategy for influenza vaccines. This article is protected by copyright. All rights reserved.

    Keywords: H3N2v; cross-protection; immunogenic; influenza; peptides.

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