Cross-protection of Lactococcus lactis-displayed HA2 subunit against homologous and heterologous influenza A viruses in mice.

Arch Virol

Department of Biotechnology, College of Life Science, Nanchang University, 330031, Nanchang, Jiangxi, China.

Published: December 2015

AI Article Synopsis

  • Current influenza vaccines are strain-specific and require annual updates, highlighting the need for a universal vaccine for broader protection.
  • The HA2 subunit of the virus shows promise for this universal vaccine, and the study explores its delivery via Lactococcus lactis using an anchor protein.
  • Results indicate that this method elicits strong immune responses and provides complete protection against both homologous and heterologous influenza strains in mice, suggesting its potential effectiveness in humans and the poultry industry.

Article Abstract

Current influenza vaccines provide strain-specific protection against homologous subtypes and need to be updated annually. Therefore, it is essential to develop a universal vaccine that would induce broadly cross-protective immunity against homologous and heterologous influenza A viruses. The highly conserved HA2 subunit is a promising candidate for developing a universal influenza vaccine. Here, we hypothesized that the HA2 subunit could be displayed on the surface of Lactococcus lactis (L. lactis), using Spax as an anchor protein (L. lactis/pNZ8008-Spax-HA2) and that L. lactis/pNZ8008-Spax-HA2 would have immunogenicity by oral administration without the use of adjuvant in the mouse model. To address this hypothesis, we show that oral vaccination of mice with L. lactis/pNZ8008-Spax-HA2 elicited significant humoral and mucosal immune responses. Importantly, L. lactis/pNZ8008-Spax-HA2 provided 100% protection against homologous H5N1 or heterologous H1N1 virus challenge. These results suggest that an HA2 subunit presented on the surface of L. lactis is an effective universal vaccine candidate against influenza A viruses in the poultry industry and in humans.

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Source
http://dx.doi.org/10.1007/s00705-015-2587-8DOI Listing

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