pmc logo imageJournal ListSearchpmc logo image
Logo of viroljBioMed Central web siteReference to the article.Search.Manuscript submission.Registration.Journal front page.
Virol J. 2008; 5: 131.
Published online 2008 October 28. doi: 10.1186/1743-422X-5-131.
PMCID: PMC2583969
Elicitation of protective immune responses using a bivalent H5N1 VLP vaccine
Corey J Crevar1 and Ted M Rosscorresponding author1,2
1Center for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA
2Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA, USA
corresponding authorCorresponding author.
Corey J Crevar: cjc63/at/pitt.edu; Ted M Ross: tmr15/at/pitt.edu
Received August 17, 2008; Accepted October 28, 2008.
Abstract

Background
Currently licensed human vaccines are subtype-specific and do not protect against pandemic H5N1 viruses. Previously, our group has reported on the construction of an influenza virus-like particle (VLP) as a new generation candidate vaccine. A mixture of influenza H5N1 VLPs representing clade 1 and 2 viruses were examined for the ability to elicit protective immunity against isolates from various clades and subclades of H5N1.

Results
Mice were vaccinated intramuscularly with each VLP individually, the mixture of VLPs, a mixture of purified recombinant hemagglutinin (rHA), or mock vaccinated. Elicited antibodies were assayed for the hemagglutination-inhibition (HAI) activity against clades 1 and clade 2 isolates. Mice vaccinated with each VLP individually or in a mixture had robust HAI responses against homologous viruses and HAI responses against the clade 2.3 virus, Anh/05. However, these vaccines did not induce an HAI response against the clade 2.2 virus, WS/05. Interestingly, clade 2 VLP vaccinated mice were protected against both clade 1 and 2 H5/PR8 viruses, but clade 1 VLP vaccinated mice were only protected against the clade 1 virus. Mice vaccinated with a mixture of VLPs were protected against both clade 1 and 2 viruses. In contrast, mice vaccinated with a mixture of rHA survived challenge, but lost ~15% of original weight by days 5–7 post-challenge.

Conclusion
These results demonstrate that a multivalent influenza VLP vaccine representing different genetic clades is a promising strategy to elicit protective immunity against isolates from emerging clades and subclades of H5N1.