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 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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Main Authors: Zamora-Ceballos, María, Moreno, Noelia, Gil-Cantero, David, Castón, José R., Blanco, Esther, Bárcena, Juan
Format: artículo biblioteca
Language:English
Published: 2022-02-02
Subjects:Virus-like particles (VLPs), Chimeric VLPs, Nanoparticles, Vaccine platform, Multivalent vaccine, RHDV, FCV, CPV, 2L21, B-cell epitope,
Online Access:http://hdl.handle.net/20.500.12792/6202
http://hdl.handle.net/10261/289603
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spelling dig-inia-es-10261-2896032023-02-16T14:54:31Z Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes Zamora-Ceballos, María Moreno, Noelia Gil-Cantero, David Castón, José R. Blanco, Esther Bárcena, Juan Virus-like particles (VLPs) Chimeric VLPs Nanoparticles Vaccine platform Multivalent vaccine RHDV FCV CPV 2L21 B-cell epitope 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. 2023-02-16T12:21:59Z 2023-02-16T12:21:59Z 2022-02-02 artículo Vaccines 10(2): e229 (2022) Multidisciplinary Digital Publishing Institute http://hdl.handle.net/20.500.12792/6202 http://hdl.handle.net/10261/289603 10.3390/vaccines10020229 2076-393X en open
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Virus-like particles (VLPs)
Chimeric VLPs
Nanoparticles
Vaccine platform
Multivalent vaccine
RHDV
FCV
CPV
2L21
B-cell epitope
Virus-like particles (VLPs)
Chimeric VLPs
Nanoparticles
Vaccine platform
Multivalent vaccine
RHDV
FCV
CPV
2L21
B-cell epitope
spellingShingle Virus-like particles (VLPs)
Chimeric VLPs
Nanoparticles
Vaccine platform
Multivalent vaccine
RHDV
FCV
CPV
2L21
B-cell epitope
Virus-like particles (VLPs)
Chimeric VLPs
Nanoparticles
Vaccine platform
Multivalent vaccine
RHDV
FCV
CPV
2L21
B-cell epitope
Zamora-Ceballos, María
Moreno, Noelia
Gil-Cantero, David
Castón, José R.
Blanco, Esther
Bárcena, Juan
Immunogenicity of Multi-Target Chimeric RHDV Virus-Like Particles Delivering Foreign B-Cell Epitopes
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.
format artículo
topic_facet Virus-like particles (VLPs)
Chimeric VLPs
Nanoparticles
Vaccine platform
Multivalent vaccine
RHDV
FCV
CPV
2L21
B-cell epitope
author Zamora-Ceballos, María
Moreno, Noelia
Gil-Cantero, David
Castón, José R.
Blanco, Esther
Bárcena, Juan
author_facet Zamora-Ceballos, María
Moreno, Noelia
Gil-Cantero, David
Castón, José R.
Blanco, Esther
Bárcena, Juan
author_sort Zamora-Ceballos, María
title 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_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_sort immunogenicity of multi-target chimeric rhdv virus-like particles delivering foreign b-cell epitopes
publishDate 2022-02-02
url http://hdl.handle.net/20.500.12792/6202
http://hdl.handle.net/10261/289603
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