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Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance

Bluetongue virus (BTV) and African horse sickness virus (AHSV) are widespread arboviruses that cause important economic losses in the livestock and equine industries, respectively. In addition to these, another arthropod-transmitted orbivirus known as epizootic hemorrhagic disease virus (EHDV) entai...

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Autores principales: Jiménez-Cabello, Luis, Utrilla-Trigo, Sergio, Barreiro-Piñeiro, Natalia, Pose-Boirazian, Tomás, Martínez-Costas, José, Marín-López, Alejandro, Ortego, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319458/
https://www.ncbi.nlm.nih.gov/pubmed/35891288
http://dx.doi.org/10.3390/vaccines10071124
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author Jiménez-Cabello, Luis
Utrilla-Trigo, Sergio
Barreiro-Piñeiro, Natalia
Pose-Boirazian, Tomás
Martínez-Costas, José
Marín-López, Alejandro
Ortego, Javier
author_facet Jiménez-Cabello, Luis
Utrilla-Trigo, Sergio
Barreiro-Piñeiro, Natalia
Pose-Boirazian, Tomás
Martínez-Costas, José
Marín-López, Alejandro
Ortego, Javier
author_sort Jiménez-Cabello, Luis
collection PubMed
description Bluetongue virus (BTV) and African horse sickness virus (AHSV) are widespread arboviruses that cause important economic losses in the livestock and equine industries, respectively. In addition to these, another arthropod-transmitted orbivirus known as epizootic hemorrhagic disease virus (EHDV) entails a major threat as there is a conducive landscape that nurtures its emergence in non-endemic countries. To date, only vaccinations with live attenuated or inactivated vaccines permit the control of these three viral diseases, although important drawbacks, e.g., low safety profile and effectiveness, and lack of DIVA (differentiation of infected from vaccinated animals) properties, constrain their usage as prophylactic measures. Moreover, a substantial number of serotypes of BTV, AHSV and EHDV have been described, with poor induction of cross-protective immune responses among serotypes. In the context of next-generation vaccine development, antigen delivery systems based on nano- or microparticles have gathered significant attention during the last few decades. A diversity of technologies, such as virus-like particles or self-assembled protein complexes, have been implemented for vaccine design against these viruses. In this work, we offer a comprehensive review of the nano- and microparticulated vaccine candidates against these three relevant orbiviruses. Additionally, we also review an innovative technology for antigen delivery based on the avian reovirus nonstructural protein muNS and we explore the prospective functionality of the nonstructural protein NS1 nanotubules as a BTV-based delivery platform.
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spelling pubmed-93194582022-07-27 Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance Jiménez-Cabello, Luis Utrilla-Trigo, Sergio Barreiro-Piñeiro, Natalia Pose-Boirazian, Tomás Martínez-Costas, José Marín-López, Alejandro Ortego, Javier Vaccines (Basel) Review Bluetongue virus (BTV) and African horse sickness virus (AHSV) are widespread arboviruses that cause important economic losses in the livestock and equine industries, respectively. In addition to these, another arthropod-transmitted orbivirus known as epizootic hemorrhagic disease virus (EHDV) entails a major threat as there is a conducive landscape that nurtures its emergence in non-endemic countries. To date, only vaccinations with live attenuated or inactivated vaccines permit the control of these three viral diseases, although important drawbacks, e.g., low safety profile and effectiveness, and lack of DIVA (differentiation of infected from vaccinated animals) properties, constrain their usage as prophylactic measures. Moreover, a substantial number of serotypes of BTV, AHSV and EHDV have been described, with poor induction of cross-protective immune responses among serotypes. In the context of next-generation vaccine development, antigen delivery systems based on nano- or microparticles have gathered significant attention during the last few decades. A diversity of technologies, such as virus-like particles or self-assembled protein complexes, have been implemented for vaccine design against these viruses. In this work, we offer a comprehensive review of the nano- and microparticulated vaccine candidates against these three relevant orbiviruses. Additionally, we also review an innovative technology for antigen delivery based on the avian reovirus nonstructural protein muNS and we explore the prospective functionality of the nonstructural protein NS1 nanotubules as a BTV-based delivery platform. MDPI 2022-07-14 /pmc/articles/PMC9319458/ /pubmed/35891288 http://dx.doi.org/10.3390/vaccines10071124 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jiménez-Cabello, Luis
Utrilla-Trigo, Sergio
Barreiro-Piñeiro, Natalia
Pose-Boirazian, Tomás
Martínez-Costas, José
Marín-López, Alejandro
Ortego, Javier
Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance
title Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance
title_full Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance
title_fullStr Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance
title_full_unstemmed Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance
title_short Nanoparticle- and Microparticle-Based Vaccines against Orbiviruses of Veterinary Importance
title_sort nanoparticle- and microparticle-based vaccines against orbiviruses of veterinary importance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319458/
https://www.ncbi.nlm.nih.gov/pubmed/35891288
http://dx.doi.org/10.3390/vaccines10071124
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