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Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
Safety and Biocompatibility of a Spray-Dried Influenza Microparticle Vaccine in Mice
A C Siddoway1,2, D Verhoeven3,2, T A Harm4
1Department of Chemical & Biological Engineering, Iowa State University, Ames, IA 50011 USA.
Abstract:
Influenza virus is a persistent source of morbidity and moribundity, and effective disease control requires ever-evolving effective vaccines. In this work, we evaluate the safety and biocompatibility of two novel polymeric particle-based influenza vaccines. Mice were immunized either intranasally or subcutaneously with these two formulations and examined at 1 h, 1 day, and 14 days post-immunization for histopathology in liver, kidneys, and lungs and serum biomarker analysis. Mice that received an intranasal vaccination were also observed for pulmonary disruption via whole body plethysmography. Examination of tissues post-immunization found only limited inflammation, with no difference observed in plethysmography measurements and no serum biomarkers (e.g., AST, AlkPhos) indicating tissue damage. Collectively, these data support the conclusion that these polymeric particle-based influenza vaccine formulations were well tolerated by the animals and did not induce any adverse side effects.
Lay Summary:
Particle-based influenza vaccines were safety tolerated by mice and did not induce any adverse side effects.
Supplementary Information:
The online version contains supplementary material available at 10.1007/s40883-025-00473-2.
Insights
Novel polymeric particle-based influenza vaccines show excellent safety and biocompatibility in mice. Studies confirmed no adverse effects or tissue damage, supporting their potential for effective influenza disease control.
Area of Science:
- Immunology
- Vaccinology
- Biomaterials Science
Background:
- Influenza virus poses a significant global health threat, necessitating continuous development of effective vaccines.
- Novel vaccine platforms are crucial for overcoming challenges associated with traditional influenza vaccines.
Purpose of the Study:
- To evaluate the safety and biocompatibility of two new polymeric particle-based influenza vaccine formulations.
- To assess potential adverse effects following intranasal and subcutaneous immunization in a mouse model.
Main Methods:
- Mice were immunized with polymeric particle-based influenza vaccines via intranasal or subcutaneous routes.
- Histopathological examination of liver, kidneys, and lungs was performed at 1 hour, 1 day, and 14 days post-immunization.
- Serum biomarker analysis and whole-body plethysmography were used to assess tissue damage and pulmonary function.
Main Results:
- Histopathology revealed only limited inflammation in immunized mice.
- No significant differences were observed in whole-body plethysmography measurements.
- Serum analysis showed no biomarkers (e.g., AST, AlkPhos) indicative of tissue damage.
Conclusions:
- The evaluated polymeric particle-based influenza vaccine formulations demonstrated good tolerability in mice.
- No adverse side effects were induced by the novel vaccine formulations.
- These findings support the potential of these particle-based vaccines for safe and effective influenza control.
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