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Expression and Purification of Virus-like Particles for Vaccination
Published on: June 2, 2016
Nano/microparticle Formulations for Universal Influenza Vaccines
Dylan A Hendy1, Eva A Amouzougan1, Isabella C Young1
1Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, 4012 Marsico Hall, 125 Mason Farm Road, Chapel Hill, North Carolina, 27599, USA.
Seasonal flu vaccines have low efficacy. Universal influenza antigens, like M2e and HA stalk, show promise when formulated with nano/microparticles, improving immunity against influenza viruses.
Area of Science:
- Vaccinology
- Nanotechnology
- Virology
Background:
- Influenza poses a significant global health threat, causing severe illness and death.
- Current seasonal influenza vaccines exhibit limited efficacy and necessitate annual updates due to viral evolution.
- Universal influenza antigens (M2e, HA stalk) offer broader protection but often lack sufficient antigenicity.
Purpose of the Study:
- To review nano/microparticle-based vaccine formulations for influenza.
- To highlight the fabrication, characterization, and immunogenicity of these advanced vaccine systems.
- To discuss future perspectives for universal influenza vaccine delivery.
Main Methods:
- Review of scientific literature on nano/microparticle carriers for influenza vaccines.
- Analysis of various materials used in particle fabrication (polymers, liposomes, metals, proteins).
- Evaluation of immune responses and protection in animal models (mice, pigs, ferrets, chickens).
Main Results:
- Nano/microparticles significantly enhance the antigenicity of universal influenza antigens.
- Diverse particle types demonstrate efficacy in inducing immunity and protection across multiple animal models.
- Physicochemical properties, fabrication methods, and biological responses are detailed for various formulations.
Conclusions:
- Nano/microparticle carriers are a promising strategy to improve the efficacy of universal influenza vaccines.
- Further research into material science and delivery systems can optimize influenza vaccine design.
- Addressing challenges in antigenicity and delivery is crucial for developing next-generation influenza vaccines.
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