Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes

The rabbit hemorrhagic disease virus (RHDV) vaccine platform is a nanoparticle composed of 180 copies of the viral capsid protein, VP60, self-assembled into virus-like particles (VLPs). RHDV VLPs are able to accept the simultaneous incorporation of target epitopes at different insertion sites. The r...

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Main Authors: María Zamora-Ceballos, Noelia Moreno, David Gil-Cantero, José R. Castón, Esther Blanco, Juan Bárcena
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/10/2/229
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author María Zamora-Ceballos
Noelia Moreno
David Gil-Cantero
José R. Castón
Esther Blanco
Juan Bárcena
author_facet María Zamora-Ceballos
Noelia Moreno
David Gil-Cantero
José R. Castón
Esther Blanco
Juan Bárcena
author_sort María Zamora-Ceballos
collection DOAJ
description The rabbit hemorrhagic disease virus (RHDV) vaccine platform is a nanoparticle composed of 180 copies of the viral capsid protein, VP60, self-assembled into virus-like particles (VLPs). RHDV VLPs are able to accept the simultaneous incorporation of target epitopes at different insertion sites. The resulting chimeric RHDV VLPs displaying immunogenic foreign antigens have been shown to induce specific protective immune responses against inserted heterologous T-cytotoxic and B-cell epitopes in the mouse and pig models. In this study, we explored whether RHDV-based engineered VLPs can be developed as efficient multivalent vaccines co-delivering different foreign B-cell antigens. We generated bivalent chimeric RHDV VLPs displaying two model B-cell epitopes at different surface-exposed insertion sites, as well as the corresponding monovalent chimeric VLPs. The immunogenic potential of the bivalent chimeric VLPs versus the monovalent constructs was assessed in the mouse model. We found that the bivalent chimeric VLPs elicited a strong and balanced antibody response towards the two target epitopes tested, although slight reductions were observed in the levels of specific serum antibody titers induced by bivalent chimeric VLPs as compared with the corresponding monovalent constructs. These results suggest that RHDV VLPs could represent a promising platform for the development of efficient multivalent vaccines.
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spelling doaj.art-a66ddbaf98754c0cb8ae28eb7a30cc4e2023-11-23T22:25:37ZengMDPI AGVaccines2076-393X2022-02-0110222910.3390/vaccines10020229Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell EpitopesMaría Zamora-Ceballos0Noelia Moreno1David Gil-Cantero2José R. Castón3Esther Blanco4Juan Bárcena5Instituto Centro de Investigación en Sanidad Animal (CISA-INIA/CSIC), Valdeolmos, 28130 Madrid, SpainInstituto Centro de Investigación en Sanidad Animal (CISA-INIA/CSIC), Valdeolmos, 28130 Madrid, SpainDepartment of Structure of Macromolecules, Centro Nacional de Biotecnología/CSIC, Cantoblanco, 28049 Madrid, SpainDepartment of Structure of Macromolecules, Centro Nacional de Biotecnología/CSIC, Cantoblanco, 28049 Madrid, SpainInstituto Centro de Investigación en Sanidad Animal (CISA-INIA/CSIC), Valdeolmos, 28130 Madrid, SpainInstituto Centro de Investigación en Sanidad Animal (CISA-INIA/CSIC), Valdeolmos, 28130 Madrid, SpainThe rabbit hemorrhagic disease virus (RHDV) vaccine platform is a nanoparticle composed of 180 copies of the viral capsid protein, VP60, self-assembled into virus-like particles (VLPs). RHDV VLPs are able to accept the simultaneous incorporation of target epitopes at different insertion sites. The resulting chimeric RHDV VLPs displaying immunogenic foreign antigens have been shown to induce specific protective immune responses against inserted heterologous T-cytotoxic and B-cell epitopes in the mouse and pig models. In this study, we explored whether RHDV-based engineered VLPs can be developed as efficient multivalent vaccines co-delivering different foreign B-cell antigens. We generated bivalent chimeric RHDV VLPs displaying two model B-cell epitopes at different surface-exposed insertion sites, as well as the corresponding monovalent chimeric VLPs. The immunogenic potential of the bivalent chimeric VLPs versus the monovalent constructs was assessed in the mouse model. We found that the bivalent chimeric VLPs elicited a strong and balanced antibody response towards the two target epitopes tested, although slight reductions were observed in the levels of specific serum antibody titers induced by bivalent chimeric VLPs as compared with the corresponding monovalent constructs. These results suggest that RHDV VLPs could represent a promising platform for the development of efficient multivalent vaccines.https://www.mdpi.com/2076-393X/10/2/229virus-like particles (VLPs)chimeric VLPsnanoparticlesvaccine platformmultivalent vaccineRHDV
spellingShingle María Zamora-Ceballos
Noelia Moreno
David Gil-Cantero
José R. Castón
Esther Blanco
Juan Bárcena
Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
Vaccines
virus-like particles (VLPs)
chimeric VLPs
nanoparticles
vaccine platform
multivalent vaccine
RHDV
title Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
title_full Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
title_fullStr Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
title_full_unstemmed Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
title_short Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
title_sort immunogenicity of multi target chimeric rhdv virus like particles delivering foreign b cell epitopes
topic virus-like particles (VLPs)
chimeric VLPs
nanoparticles
vaccine platform
multivalent vaccine
RHDV
url https://www.mdpi.com/2076-393X/10/2/229
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