Cargando…
Vectored vaccines to protect against PRRSV
PRRSV is the causative agent of the most important infectious disease affecting swine herds worldwide, producing great economic losses. Commercially available vaccines are only partially effective in protection against PRRSV. Moreover, modified live vaccines may allow virus shedding, and could rever...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114413/ https://www.ncbi.nlm.nih.gov/pubmed/20600388 http://dx.doi.org/10.1016/j.virusres.2010.06.017 |
_version_ | 1783513880289345536 |
---|---|
author | Cruz, Jazmina L.G. Zúñiga, Sonia Bécares, Martina Sola, Isabel Ceriani, Juan E. Juanola, Sandra Plana, Juan Enjuanes, Luis |
author_facet | Cruz, Jazmina L.G. Zúñiga, Sonia Bécares, Martina Sola, Isabel Ceriani, Juan E. Juanola, Sandra Plana, Juan Enjuanes, Luis |
author_sort | Cruz, Jazmina L.G. |
collection | PubMed |
description | PRRSV is the causative agent of the most important infectious disease affecting swine herds worldwide, producing great economic losses. Commercially available vaccines are only partially effective in protection against PRRSV. Moreover, modified live vaccines may allow virus shedding, and could revert generating virulent phenotypes. Therefore, new efficient vaccines are required. Vaccines based on recombinant virus genomes (virus vectored vaccines) against PRRSV could represent a safe alternative for the generation of modified live vaccines. In this paper, current vectored vaccines to protect against PRRSV are revised, including those based on pseudorabies virus, poxvirus, adenovirus, and virus replicons. Special attention has been provided to the use of transmissible gastroenteritis virus (TGEV) as vector for the expression of PRRSV antigens. This vector has the capability of expressing high levels of heterologous genes, is a potent interferon-α inducer, and presents antigens in mucosal surfaces, eliciting both secretory and systemic immunity. A TGEV derived vector (rTGEV) was generated, expressing PRRSV wild type or modified GP5 and M proteins, described as the main inducers of neutralizing antibodies and cellular immune response, respectively. Protection experiments showed that vaccinated animals developed a faster and stronger humoral immune response than the non-vaccinated ones. Partial protection in challenged animals was observed, as vaccinated pigs showed decreased lung damage when compared with the non-vaccinated ones. Nevertheless, the level of neutralizing antibodies was low, what may explain the limited protection observed. Several strategies are proposed to improve current rTGEV vectors expressing PRRSV antigens. |
format | Online Article Text |
id | pubmed-7114413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71144132020-04-02 Vectored vaccines to protect against PRRSV Cruz, Jazmina L.G. Zúñiga, Sonia Bécares, Martina Sola, Isabel Ceriani, Juan E. Juanola, Sandra Plana, Juan Enjuanes, Luis Virus Res Review PRRSV is the causative agent of the most important infectious disease affecting swine herds worldwide, producing great economic losses. Commercially available vaccines are only partially effective in protection against PRRSV. Moreover, modified live vaccines may allow virus shedding, and could revert generating virulent phenotypes. Therefore, new efficient vaccines are required. Vaccines based on recombinant virus genomes (virus vectored vaccines) against PRRSV could represent a safe alternative for the generation of modified live vaccines. In this paper, current vectored vaccines to protect against PRRSV are revised, including those based on pseudorabies virus, poxvirus, adenovirus, and virus replicons. Special attention has been provided to the use of transmissible gastroenteritis virus (TGEV) as vector for the expression of PRRSV antigens. This vector has the capability of expressing high levels of heterologous genes, is a potent interferon-α inducer, and presents antigens in mucosal surfaces, eliciting both secretory and systemic immunity. A TGEV derived vector (rTGEV) was generated, expressing PRRSV wild type or modified GP5 and M proteins, described as the main inducers of neutralizing antibodies and cellular immune response, respectively. Protection experiments showed that vaccinated animals developed a faster and stronger humoral immune response than the non-vaccinated ones. Partial protection in challenged animals was observed, as vaccinated pigs showed decreased lung damage when compared with the non-vaccinated ones. Nevertheless, the level of neutralizing antibodies was low, what may explain the limited protection observed. Several strategies are proposed to improve current rTGEV vectors expressing PRRSV antigens. Elsevier B.V. 2010-12 2010-06-25 /pmc/articles/PMC7114413/ /pubmed/20600388 http://dx.doi.org/10.1016/j.virusres.2010.06.017 Text en Copyright © 2010 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Cruz, Jazmina L.G. Zúñiga, Sonia Bécares, Martina Sola, Isabel Ceriani, Juan E. Juanola, Sandra Plana, Juan Enjuanes, Luis Vectored vaccines to protect against PRRSV |
title | Vectored vaccines to protect against PRRSV |
title_full | Vectored vaccines to protect against PRRSV |
title_fullStr | Vectored vaccines to protect against PRRSV |
title_full_unstemmed | Vectored vaccines to protect against PRRSV |
title_short | Vectored vaccines to protect against PRRSV |
title_sort | vectored vaccines to protect against prrsv |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114413/ https://www.ncbi.nlm.nih.gov/pubmed/20600388 http://dx.doi.org/10.1016/j.virusres.2010.06.017 |
work_keys_str_mv | AT cruzjazminalg vectoredvaccinestoprotectagainstprrsv AT zunigasonia vectoredvaccinestoprotectagainstprrsv AT becaresmartina vectoredvaccinestoprotectagainstprrsv AT solaisabel vectoredvaccinestoprotectagainstprrsv AT cerianijuane vectoredvaccinestoprotectagainstprrsv AT juanolasandra vectoredvaccinestoprotectagainstprrsv AT planajuan vectoredvaccinestoprotectagainstprrsv AT enjuanesluis vectoredvaccinestoprotectagainstprrsv |