Inactivated influenza vaccines (IIVs) lack broad efficacy. Cellular immunity to a conserved internal antigen, the nucleoprotein (NP), has been correlated to protection against pandemic and seasonal influenza and thus could have the potential to broaden vaccine efficacy. We developed OVX836, a recombinant protein vaccine based on an oligomerized NP, which shows increased uptake by dendritic cells and immunogenicity compared with NP. Intramuscular immunization in mice with OVX836 induced strong NP-specific CD4+ and CD8+ T-cell systemic responses and established CD8+ tissue memory T cells in the lung parenchyma. Strikingly, OVX836 protected mice against viral challenge with three different influenza A subtypes, isolated several decades apart and induced a reduction in viral load. When co-administered with IIV, OVX836 was even more effective in reducing lung viral load.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344521PMC
http://dx.doi.org/10.1038/s41541-019-0098-4DOI Listing

Publication Analysis

Top Keywords

ovx836 recombinant
8
influenza subtypes
8
viral load
8
ovx836
5
recombinant nucleoprotein
4
nucleoprotein vaccine
4
vaccine inducing
4
inducing cellular
4
cellular responses
4
responses protective
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!