Analysis of the efficacy of an adjuvant-based inactivated pandemic H5N1 influenza virus vaccine
Autor: | Amanzhol Makbuz, N. M. Rametov, Yevgeniy Volgin, Markhabat Kassenov, Altynay Sagymbay, Ainur Nurpeisova, Berik Khairullin, Kaissar Tabynov, Abylay Sansyzbay, Gourapura J. Renukaradhya |
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Rok vydání: | 2019 |
Předmět: |
Male
medicine.medical_treatment Hemagglutinin (influenza) Hemagglutinin Glycoproteins Influenza Virus Biology Antibodies Viral medicine.disease_cause Virus Mice 03 medical and health sciences Adjuvants Immunologic Antigen Neutralization Tests Virology Influenza Human Influenza A virus medicine Animals Humans Microneutralization Assay Pandemics 030304 developmental biology Mice Inbred BALB C 0303 health sciences Influenza A Virus H5N1 Subtype 030306 microbiology Immunogenicity Ferrets General Medicine Influenza A virus subtype H5N1 Vaccines Inactivated Influenza Vaccines biology.protein Female Adjuvant |
Zdroj: | Archives of Virology. 164:1027-1036 |
ISSN: | 1432-8798 0304-8608 |
DOI: | 10.1007/s00705-019-04147-7 |
Popis: | This paper describes a preclinical study analyzing the immunogenicity and protective efficacy of Kazfluvac®, an adjuvant-based inactivated pandemic influenza A/H5N1 virus vaccine. In this study, laboratory animals (ferrets and mice) were vaccinated by the intramuscular or intraperitoneal route at an interval of 14 days with two doses of the vaccine containing different concentrations of influenza virus hemagglutinin (HA) protein. HA protein without adjuvant (aluminum hydroxide and Merthiolate) was used as a control. As a negative control, we utilized PBS. We assessed the protective efficacy of the candidate vaccine by analyzing the response to challenge with the influenza virus strain A/chicken/Astana/6/05 (H5N1). Our experimental results revealed substantially reduced clinical disease and an increased antibody response, as determined by hemagglutination-inhibition (HAI) test and microneutralization assay (MNA). This study showed that the candidate vaccine is safe and elicits an antigen-dose-dependent serum antibody response. In summary, we determined the optimum antigen dose in a Kazfluvac® adjuvant formulation required for induction of heightened immunogenicity and protective efficacy to mitigate H5N1 disease in experimental animals, suggesting its readiness for clinical studies in humans. |
Databáze: | OpenAIRE |
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