Multiple subtypes of avian influenza virus (AIV), including H5N1, H5N6, and H5N8 viruses, are currently co-circulating in wild birds and poultry and causing sporadic human infections. Vaccine development is essential for pandemic preparedness. In this study, we constructed a candidate vaccine virus (CVV) using reverse genetics (RG) based on the sequence of the first human-infected H5N8 subtype AIV, A/Astrakhan/3212/2020 (H5N8). We evaluated the immunogenicity of the rH5N8/PR8 vaccine strain in combination with Alum, ISA51, and MF59 adjuvants, and we optimized immunization strategies including dosage, administration route, and immunization interval in BALB/c mice. Our results demonstrated that a 10 μg dose of inactivated rH5N8/PR8 with MF59 adjuvant, administered intramuscularly twice at 7-day intervals, induced the strongest immune response and effectively protected mice against challenge with wild-type H5N8 AIVs. Since pandemic influenza vaccines typically require tailored vaccination doses and routes specific to their characteristics, this study provides valuable insights for the development of similar vaccine strains with pandemic potential.
Construction and Immune Strategy Optimization of a Vaccine Strain for Influenza A (H5N8) Subtype
Shuxia Zhang,Jing Tang,Li-qi Liu,He-jiang Wei,Li Xin,Kang Xiao,Jinbo Xiao,Jie Dong,Zi Li,Hongyan Bai,Shuaixing Wang,Wenfei Zhu,Lei Yang,Shu-mei Zou,Dayan Wang
Published 2025 in Viruses
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- Publication year
2025
- Venue
Viruses
- Publication date
2025-04-01
- Fields of study
Biology, Medicine, Environmental Science
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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