Cargando…

Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections

The Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) is the etiological agent of one of the most important swine diseases with a significant economic burden worldwide. Unfortunately, available vaccines are partially effective highlighting the need of novel approaches. Previously, antigeni...

Descripción completa

Detalles Bibliográficos
Autores principales: Montaner-Tarbes, Sergio, Novell, Elena, Tarancón, Vicens, Borrás, Francesc E., Montoya, Maria, Fraile, Lorenzo, del Portillo, Hernando A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269534/
https://www.ncbi.nlm.nih.gov/pubmed/30504834
http://dx.doi.org/10.1038/s41598-018-36141-5
_version_ 1783376491370774528
author Montaner-Tarbes, Sergio
Novell, Elena
Tarancón, Vicens
Borrás, Francesc E.
Montoya, Maria
Fraile, Lorenzo
del Portillo, Hernando A.
author_facet Montaner-Tarbes, Sergio
Novell, Elena
Tarancón, Vicens
Borrás, Francesc E.
Montoya, Maria
Fraile, Lorenzo
del Portillo, Hernando A.
author_sort Montaner-Tarbes, Sergio
collection PubMed
description The Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) is the etiological agent of one of the most important swine diseases with a significant economic burden worldwide. Unfortunately, available vaccines are partially effective highlighting the need of novel approaches. Previously, antigenic viral proteins were described in serum-derived extracellular vesicles (EVs) from pigs previously infected with PRRSV. Here, a targeted-pig trial was designed to determine the safety and immunogenicity of such extracellular vesicles enriched fractions. Our results showed that immunizations with EV-enriched fractions from convalescence animals in combination with montanide is safe and free of virus as immunizations with up-to two milligrams of EV-enriched fractions did not induce clinical symptoms, adverse effects and detectable viral replication. In addition, this vaccine formulation was able to elicit specific humoral IgG immune response in vaccinated animals, albeit variably. Noticeably, sera from vaccinated animals was diagnosed negative when tested for PRRSV using a commercial ELISA test; thus, indicating that this new approach differentiates vaccinated from infected animals. Lastly, after priming animals with EV-enriched fractions from sera of convalescence animals and boosting them with synthetic viral peptides identified by mass spectrometry, a distinctive high and specific IFN-γ response was elicited. Altogether, our data strongly suggest the use of serum EV-enriched fractions as a novel vaccine strategy against PRRSV.
format Online
Article
Text
id pubmed-6269534
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62695342018-12-04 Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections Montaner-Tarbes, Sergio Novell, Elena Tarancón, Vicens Borrás, Francesc E. Montoya, Maria Fraile, Lorenzo del Portillo, Hernando A. Sci Rep Article The Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) is the etiological agent of one of the most important swine diseases with a significant economic burden worldwide. Unfortunately, available vaccines are partially effective highlighting the need of novel approaches. Previously, antigenic viral proteins were described in serum-derived extracellular vesicles (EVs) from pigs previously infected with PRRSV. Here, a targeted-pig trial was designed to determine the safety and immunogenicity of such extracellular vesicles enriched fractions. Our results showed that immunizations with EV-enriched fractions from convalescence animals in combination with montanide is safe and free of virus as immunizations with up-to two milligrams of EV-enriched fractions did not induce clinical symptoms, adverse effects and detectable viral replication. In addition, this vaccine formulation was able to elicit specific humoral IgG immune response in vaccinated animals, albeit variably. Noticeably, sera from vaccinated animals was diagnosed negative when tested for PRRSV using a commercial ELISA test; thus, indicating that this new approach differentiates vaccinated from infected animals. Lastly, after priming animals with EV-enriched fractions from sera of convalescence animals and boosting them with synthetic viral peptides identified by mass spectrometry, a distinctive high and specific IFN-γ response was elicited. Altogether, our data strongly suggest the use of serum EV-enriched fractions as a novel vaccine strategy against PRRSV. Nature Publishing Group UK 2018-11-30 /pmc/articles/PMC6269534/ /pubmed/30504834 http://dx.doi.org/10.1038/s41598-018-36141-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Montaner-Tarbes, Sergio
Novell, Elena
Tarancón, Vicens
Borrás, Francesc E.
Montoya, Maria
Fraile, Lorenzo
del Portillo, Hernando A.
Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections
title Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections
title_full Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections
title_fullStr Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections
title_full_unstemmed Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections
title_short Targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from Porcine Respiratory and Reproductive virus infections
title_sort targeted-pig trial on safety and immunogenicity of serum-derived extracellular vesicles enriched fractions obtained from porcine respiratory and reproductive virus infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269534/
https://www.ncbi.nlm.nih.gov/pubmed/30504834
http://dx.doi.org/10.1038/s41598-018-36141-5
work_keys_str_mv AT montanertarbessergio targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections
AT novellelena targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections
AT taranconvicens targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections
AT borrasfrancesce targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections
AT montoyamaria targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections
AT frailelorenzo targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections
AT delportillohernandoa targetedpigtrialonsafetyandimmunogenicityofserumderivedextracellularvesiclesenrichedfractionsobtainedfromporcinerespiratoryandreproductivevirusinfections