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Updated: Oct 5, 2025

Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
Polycationic HA/CpG Nanoparticles Induce Cross-Protective Influenza Immunity in Mice
Chunhong Dong1, Ye Wang1, Wandi Zhu1
1Center for Inflammation, Immunity & Infection, Georgia State University Institute for Biomedical Sciences, Atlanta, Georgia 30303, United States.
Intranasal influenza vaccines using polyethylenimine (PEI) nanoparticles with hemagglutinin (HA) and CpG adjuvants show promise. These PEI-HA/CpG nanoparticles enhance immune responses and provide cross-protection against influenza.
Area of Science:
- Immunology
- Nanotechnology
- Vaccinology
Background:
- The intranasal (i.n.) route is optimal for respiratory disease vaccines.
- Polycationic polyethylenimine (PEI) can form nanoparticles with viral glycoproteins.
Purpose of the Study:
- To fabricate and evaluate PEI-HA and PEI-HA/CpG nanoparticles for i.n. influenza vaccination.
- To investigate their immunogenicity, protective efficacy, and immune response profiles.
Main Methods:
- Fabrication of PEI-hemagglutinin (HA) and PEI-HA/CpG nanoparticles.
- Intranasal vaccination regimen in mice.
- Assessment of immune responses, including antibody production and cellular immunity.
- Evaluation of heterologous cross-protection.
Main Results:
- Nanoparticles significantly enhanced HA immunogenicity and provided cross-protection.
- PEI-HA/CpG nanoparticles induced robust, balanced IgG1/IgG2a responses with enhanced neutralization and ADCC.
- Both local and systemic cellular immunity were augmented and sustained for six months.
- PEI and CpG demonstrated synergistic effects on immune responses.
Conclusions:
- PEI-HA/CpG nanoparticles represent a potential cross-protective influenza vaccine candidate.
- Polycationic PEI nanoplatforms are promising for mucosal vaccine development.
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