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Updated: Jun 15, 2026

Expression and Purification of Virus-like Particles for Vaccination
Published on: June 2, 2016
Norwalk virus-like particles as vaccines
Melissa Herbst-Kralovetz1, Hugh S Mason, Qiang Chen
1Center for Infectious Diseases and Vaccinology, Biodesign Institute at Arizona State University, Tempe, AZ 85287, USA and Dept of Basic Medical Sciences, The University of Arizona College of Medicine-Phoenix in Partnership with Arizona State University, Phoenix, AZ 85004, USA. melissa.herbst-kralovetz@asu.edu
Norovirus virus-like particles (VLPs) are immunogenic and can be produced in various systems. These norovirus VLPs show potential as effective vaccine delivery vehicles for heterologous peptide antigens.
Area of Science:
- Virology
- Vaccinology
- Biotechnology
Background:
- Noroviruses (NoV) are a leading cause of epidemic nonbacterial gastroenteritis in humans.
- Recombinant expression of norovirus capsid proteins yields virus-like particles (VLPs) that mimic authentic virions.
- Norwalk virus-like particles (NVLPs) are acid- and heat-stable, and immunogenic.
Purpose of the Study:
- To evaluate the potential of norovirus VLPs as vaccine-delivery vehicles.
- To investigate the immunogenicity of NVLPs via oral and nasal delivery.
- To explore the feasibility of using NVLPs for delivering heterologous peptide antigens.
Main Methods:
- Expression of norovirus capsid proteins in insect and plant cells to produce VLPs.
- Oral and intranasal administration of NVLPs in mice and humans.
- Analysis of systemic and mucosal antibody responses.
- Identification of potential sites for foreign peptide insertion on VLP surface structures.
Main Results:
- NVLPs produced in insect cells and plants are immunogenic in mice and humans upon oral delivery.
- Intranasal delivery of NVLPs elicits high antibody levels at lower doses compared to oral delivery.
- Oral and nasal NVLP delivery stimulate antibodies at distal mucosal sites.
- Surface structure analysis identified suitable sites for foreign peptide insertion without compromising VLP assembly or receptor binding.
Conclusions:
- Norovirus VLPs, particularly NVLPs, are promising vaccine candidates due to their immunogenicity and stability.
- NVLPs can be effectively delivered orally and intranasally, inducing robust mucosal immunity.
- Norovirus VLPs have significant potential as versatile vaccine-delivery platforms for heterologous antigens.
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