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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7565419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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