Related Experiment Video
Updated: Aug 6, 2026

Detection of Neutralization-sensitive Epitopes in Antigens Displayed on Virus-Like Particle (VLP)-Based Vaccines Using a Capture Assay
Published on: February 10, 2022
Virus-like particles derived from major capsid protein VP1 of different polyomaviruses differ in their ability to
Alma Gedvilaite1, David C Dorn, Kestutis Sasnauskas
1Institute of Biotechnology, V Graiciuno 8, LT-02241 Vilnius, Lithuania.
Abstract:
As polyomavirus major capsid protein VP1-derived virus-like particles (VLPs) have been demonstrated to be highly immunogenic, we studied their interaction with human dendritic cells (hDCs). Exposure of hDCs to VLPs originating from murine (MPyV) or hamster polyomavirus (HaPyV) induced hDC maturation. In contrast, exposure of hDCs to VLPs derived from human polyomaviruses (BK and JC) and simian virus 40 (SV40) only marginally induced DC maturation. The hDCs stimulated by HaPyV- or MPyV-derived VLPs readily produced interleukin-12 and stimulated CD8-positive T-cell responses in vitro. The highest frequencies of activated T cells were again observed after pulsing with HaPyV- and MPyV-derived VLPs. Monocyte-derived hDCs both bound and internalized the various tested polyomavirus VP1-derived VLPs with different levels of efficiency, partially explaining their individual maturation potentials. In conclusion, our data suggest a high variability in uptake of polyomavirus-derived VLPs and potency to induce hDC maturation.
Insights
Murine and hamster polyomavirus VP1 virus-like particles (VLPs) effectively mature human dendritic cells (hDCs) and stimulate T-cell responses. Other polyomavirus VLPs showed limited impact, indicating variable VLP potency.
Area of Science:
- Immunology
- Virology
- Cell Biology
Background:
- Polyomavirus major capsid protein VP1-derived virus-like particles (VLPs) are known for their high immunogenicity.
- Understanding VLP interactions with immune cells is crucial for vaccine development.
Purpose of the Study:
- To investigate the interaction between various polyomavirus VP1-derived VLPs and human dendritic cells (hDCs).
- To assess the capacity of different polyomavirus VLPs to induce hDC maturation and T-cell responses.
Main Methods:
- Exposure of human dendritic cells (hDCs) to VLPs from murine (MPyV), hamster (HaPyV), human (BK, JC), and simian virus 40 (SV40) polyomaviruses.
- Analysis of hDC maturation markers, cytokine production (interleukin-12), and CD8-positive T-cell activation in vitro.
- Assessment of VLP binding and internalization by monocyte-derived hDCs.
Main Results:
- VLPs from MPyV and HaPyV significantly induced hDC maturation, interleukin-12 production, and CD8+ T-cell responses.
- VLPs from human polyomaviruses (BK, JC) and SV40 showed only marginal effects on hDC maturation.
- Differential binding and internalization efficiencies of polyomavirus VLPs by hDCs were observed, correlating with maturation potential.
Conclusions:
- Polyomavirus-derived VLPs exhibit significant variability in their uptake by hDCs and their potency to induce hDC maturation.
- MPyV and HaPyV VLPs are potent inducers of hDC maturation and T-cell responses, suggesting potential for immunomodulatory applications.
More Related Videos
09:08Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
Published on: July 27, 2021
08:10Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses
Published on: January 15, 2020
Related Concept Videos
Inhibitors of Virion Maturation and Assembly
Viral Structure
Immune Response Against Viral Pathogens
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
Introduction to Virus
Subviral Agents
Poliomyelitis