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Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus

A broadly protective and biosafe vaccine against foot-and-mouth disease virus (FMDV) remains an unmet need in the animal health sector. We have previously reported solid protection against serotype O FMDV afforded by dendrimeric peptide structures harboring virus-specific B- and T-cell epitopes, and...

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Autores principales: Defaus, Sira, Forner, Mar, Cañas-Arranz, Rodrigo, de León, Patricia, Bustos, María J., Rodríguez-Pulido, Miguel, Blanco, Esther, Sobrino, Francisco, Andreu, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565419/
https://www.ncbi.nlm.nih.gov/pubmed/32707834
http://dx.doi.org/10.3390/vaccines8030406
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author Defaus, Sira
Forner, Mar
Cañas-Arranz, Rodrigo
de León, Patricia
Bustos, María J.
Rodríguez-Pulido, Miguel
Blanco, Esther
Sobrino, Francisco
Andreu, David
author_facet Defaus, Sira
Forner, Mar
Cañas-Arranz, Rodrigo
de León, Patricia
Bustos, María J.
Rodríguez-Pulido, Miguel
Blanco, Esther
Sobrino, Francisco
Andreu, David
author_sort Defaus, Sira
collection PubMed
description A broadly protective and biosafe vaccine against foot-and-mouth disease virus (FMDV) remains an unmet need in the animal health sector. We have previously reported solid protection against serotype O FMDV afforded by dendrimeric peptide structures harboring virus-specific B- and T-cell epitopes, and also shown such type of multivalent presentations to be advantageous over simple B-T-epitope linear juxtaposition. Chemically, our vaccine platforms are modular constructions readily made from specified B- and T-cell epitope precursor peptides that are conjugated in solution. With the aim of developing an improved version of our formulations to be used for on-demand vaccine applications, we evaluate in this study a novel design for epitope presentation to the immune system based on a multiple antigen peptide (MAP) containing six immunologically relevant motifs arranged in dendrimeric fashion (named B(2)T-TB(2)). Interestingly, two B(2)T units fused tail-to-tail into a single homodimer platform elicited higher B- and T-cell specific responses than former candidates, with immunization scores remaining stable even after 4 months. Moreover, this macromolecular assembly shows consistent immune response in swine, the natural FMDV host, at reduced dose. Thus, our versatile, immunogenic prototype can find application in the development of peptide-based vaccine candidates for various therapeutic uses using safer and more efficacious vaccination regimens.
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spelling pubmed-75654192020-10-26 Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus Defaus, Sira Forner, Mar Cañas-Arranz, Rodrigo de León, Patricia Bustos, María J. Rodríguez-Pulido, Miguel Blanco, Esther Sobrino, Francisco Andreu, David Vaccines (Basel) Article A broadly protective and biosafe vaccine against foot-and-mouth disease virus (FMDV) remains an unmet need in the animal health sector. We have previously reported solid protection against serotype O FMDV afforded by dendrimeric peptide structures harboring virus-specific B- and T-cell epitopes, and also shown such type of multivalent presentations to be advantageous over simple B-T-epitope linear juxtaposition. Chemically, our vaccine platforms are modular constructions readily made from specified B- and T-cell epitope precursor peptides that are conjugated in solution. With the aim of developing an improved version of our formulations to be used for on-demand vaccine applications, we evaluate in this study a novel design for epitope presentation to the immune system based on a multiple antigen peptide (MAP) containing six immunologically relevant motifs arranged in dendrimeric fashion (named B(2)T-TB(2)). Interestingly, two B(2)T units fused tail-to-tail into a single homodimer platform elicited higher B- and T-cell specific responses than former candidates, with immunization scores remaining stable even after 4 months. Moreover, this macromolecular assembly shows consistent immune response in swine, the natural FMDV host, at reduced dose. Thus, our versatile, immunogenic prototype can find application in the development of peptide-based vaccine candidates for various therapeutic uses using safer and more efficacious vaccination regimens. MDPI 2020-07-22 /pmc/articles/PMC7565419/ /pubmed/32707834 http://dx.doi.org/10.3390/vaccines8030406 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Defaus, Sira
Forner, Mar
Cañas-Arranz, Rodrigo
de León, Patricia
Bustos, María J.
Rodríguez-Pulido, Miguel
Blanco, Esther
Sobrino, Francisco
Andreu, David
Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus
title Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus
title_full Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus
title_fullStr Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus
title_full_unstemmed Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus
title_short Designing Functionally Versatile, Highly Immunogenic Peptide-Based Multiepitopic Vaccines against Foot-and-Mouth Disease Virus
title_sort designing functionally versatile, highly immunogenic peptide-based multiepitopic vaccines against foot-and-mouth disease virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565419/
https://www.ncbi.nlm.nih.gov/pubmed/32707834
http://dx.doi.org/10.3390/vaccines8030406
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