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Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine
OBJECTIVE: Infection of chickens with low pathogenic avian influenza virus, such as H9N2 virus, culminates in decreased egg production and increased mortality and morbidity if co-infection with other respiratory pathogens occurs. We have previously observed the induction of antibody- and cell-mediat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029274/ https://www.ncbi.nlm.nih.gov/pubmed/29970157 http://dx.doi.org/10.1186/s13104-018-3537-9 |
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author | Astill, Jake Alkie, Tamiru Yitbarek, Alexander Taha-Abdelaziz, Khaled Bavananthasivam, Jegarubee Nagy, Éva Petrik, James John Sharif, Shayan |
author_facet | Astill, Jake Alkie, Tamiru Yitbarek, Alexander Taha-Abdelaziz, Khaled Bavananthasivam, Jegarubee Nagy, Éva Petrik, James John Sharif, Shayan |
author_sort | Astill, Jake |
collection | PubMed |
description | OBJECTIVE: Infection of chickens with low pathogenic avian influenza virus, such as H9N2 virus, culminates in decreased egg production and increased mortality and morbidity if co-infection with other respiratory pathogens occurs. We have previously observed the induction of antibody- and cell-mediated immune responses after intramuscular administration of an H9N2 beta-propiolactone inactivated virus vaccine to chickens. Given the fact that in ovo vaccination represents a practical option for vaccination against H9N2 AIV in chickens, in the current study, we set out to characterize immune responses in chickens against a beta-propiolactone inactivated H9N2 virus vaccine after primary vaccination in ovo on embryonic day 18, and secondary intramuscular vaccination on day 14 post-hatch. We also included the Toll-like receptor 21 ligand, CpG ODN 2007, and an oil emulsion adjuvant, AddaVax™, as adjuvants for the vaccines. RESULTS: Antibody-mediated immune responses were observed after administering the secondary intramuscular vaccine. Cell-mediated immune responses were observed in chickens that received the beta-propiolactone inactivated H9N2 virus combined with AddaVax™. Our results demonstrate that adaptive immune responses can be induced in chickens after a primary in ovo vaccination and secondary intramuscular vaccination. |
format | Online Article Text |
id | pubmed-6029274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60292742018-07-09 Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine Astill, Jake Alkie, Tamiru Yitbarek, Alexander Taha-Abdelaziz, Khaled Bavananthasivam, Jegarubee Nagy, Éva Petrik, James John Sharif, Shayan BMC Res Notes Research Note OBJECTIVE: Infection of chickens with low pathogenic avian influenza virus, such as H9N2 virus, culminates in decreased egg production and increased mortality and morbidity if co-infection with other respiratory pathogens occurs. We have previously observed the induction of antibody- and cell-mediated immune responses after intramuscular administration of an H9N2 beta-propiolactone inactivated virus vaccine to chickens. Given the fact that in ovo vaccination represents a practical option for vaccination against H9N2 AIV in chickens, in the current study, we set out to characterize immune responses in chickens against a beta-propiolactone inactivated H9N2 virus vaccine after primary vaccination in ovo on embryonic day 18, and secondary intramuscular vaccination on day 14 post-hatch. We also included the Toll-like receptor 21 ligand, CpG ODN 2007, and an oil emulsion adjuvant, AddaVax™, as adjuvants for the vaccines. RESULTS: Antibody-mediated immune responses were observed after administering the secondary intramuscular vaccine. Cell-mediated immune responses were observed in chickens that received the beta-propiolactone inactivated H9N2 virus combined with AddaVax™. Our results demonstrate that adaptive immune responses can be induced in chickens after a primary in ovo vaccination and secondary intramuscular vaccination. BioMed Central 2018-07-03 /pmc/articles/PMC6029274/ /pubmed/29970157 http://dx.doi.org/10.1186/s13104-018-3537-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Astill, Jake Alkie, Tamiru Yitbarek, Alexander Taha-Abdelaziz, Khaled Bavananthasivam, Jegarubee Nagy, Éva Petrik, James John Sharif, Shayan Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine |
title | Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine |
title_full | Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine |
title_fullStr | Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine |
title_full_unstemmed | Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine |
title_short | Induction of immune response in chickens primed in ovo with an inactivated H9N2 avian influenza virus vaccine |
title_sort | induction of immune response in chickens primed in ovo with an inactivated h9n2 avian influenza virus vaccine |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029274/ https://www.ncbi.nlm.nih.gov/pubmed/29970157 http://dx.doi.org/10.1186/s13104-018-3537-9 |
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