THE AIM
A preclinical study of the immunogenicity and protective properties of the influenza trivalent vaccine AdeVac-FluTM in laboratory mice BALB/c strain.
MATERIAL AND METHODS
The vaccine AdeVac-FluTM is a mixture of recombinant human adenovirus 5 serotype encoding the hemagglutinin genes of influenza virus vaccine strains: A/California/07/2009 (H1N1), A/Perth/16/2009(H3N2), B/Brisbane/60/2008, as well as the molecular adjuvant Immunomax. As a reference drug, was used the live influenza virus vaccine Ultravak, produced by the FSUE SPA «Microgen». Balb/c mice were immunized once with AdeVac-FluTM intranasally and 28 days after immunization were infected with a lethal dose of influenza viruses A H1N1, H3N2 and influenza virus B. The level of virus accumulation in the lungs of infected mice was evaluated at 3 and 6 days after infection by titration the lung homogenates in MDCK cells. Evaluation of the humoral immune response to influenza viruses was performed by ELISA, HIA and VNA.
RESULTS
It was shown that the influenza vaccine AdeVac-FluTM is more immunogenic than the reference drug. Protection quality against homologous strains of influenza viruses via AdeVac-FluTM are either slightly lower or comparable to the reference drug. At the same time, it was shown that AdeVac-FluTM, as well as a live influenza virus vaccine, protects mice from a heterologous strain of the influenza virus, despite the fact that mice immunized with AdeVac-FluTM showed virus excretion from the lungs and a slight decrease in body weight (less than 10%).
CONCLUSIONS
AdeVac-FluTM vaccine based on recombinant human adenoviruses 5 serotype encoding the hemagglutinin genes of influenza viruses A/California/07/2009(H1N1), A/Perth/16/2009(H3N2), B/Brisbane/60/2008, possesses immunogenicity and protective properties in relation to both homologous and heterologous (within the subtype) strains of the influenza virus.