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Updated: Jan 30, 2026

Expression and Purification of Virus-like Particles for Vaccination
Published on: June 2, 2016
Efficient oral vaccination by bioengineering virus-like particles with protozoan surface proteins
Marianela C Serradell1, Lucía L Rupil1,2, Román A Martino1,3
1Centro de Investigación y Desarrollo en Inmunología y Enfermedades Infecciosas (CIDIE), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)/Universidad Católica de Córdoba (UCC), Córdoba, X5016DHK, Argentina.
Variant-specific surface proteins (VSPs) from Giardia lamblia offer protection and stimulate immunity. This discovery enables a novel oral vaccine platform using VSP-decorated virus-like particles (VLPs) for enhanced efficacy and stability.
Area of Science:
- Parasitology
- Immunology
- Vaccinology
Background:
- Protozoa like Giardia lamblia use variant-specific surface proteins (VSPs) for protection.
- VSPs exhibit resistance to harsh conditions and modulate host immune responses via TLR-4.
- These VSP properties present an opportunity for developing oral vaccine adjuvants and delivery systems.
Purpose of the Study:
- To investigate the potential of VSPs as protective and adjuvant components for oral vaccines.
- To develop and evaluate chimeric virus-like particles (VLPs) decorated with VSPs for antigen delivery.
- To assess the immunogenicity and protective efficacy of VSP-pseudotyped VLPs against influenza and tumors.
Main Methods:
- Constructed chimeric VLPs displaying VSPs and model antigens (influenza HA and NA).
- Assessed VLP stability against degradation and their ability to activate antigen-presenting cells in vitro.
- Administered VSP-pseudotyped VLPs orally to mice and evaluated immune responses and protection against influenza infection and tumors.
Main Results:
- VSP-decorated VLPs demonstrated resistance to degradation and activated antigen-presenting cells.
- Oral administration of VSP-pseudotyped VLPs induced robust immune responses in mice.
- Mice vaccinated with VSP-VLPs were protected from influenza infection and showed reduced growth of HA-expressing tumors.
Conclusions:
- VSPs can be leveraged to create stable and immunogenic oral vaccine platforms.
- VSP-pseudotyped VLPs represent a promising strategy for developing safe and effective oral vaccines.
- This versatile platform demonstrates potential for combating infectious diseases and cancer.
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