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Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken
Live intermediate plus infectious bursal disease virus (IBDV) vaccines (hot vaccines) are used for protection against the virulent IBDV strains in young chickens. We evaluated the potential of Toll-like receptor (TLR) agonists to alleviate hot vaccine-induced immunosuppression. The combination of Pa...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547722/ https://www.ncbi.nlm.nih.gov/pubmed/31160675 http://dx.doi.org/10.1038/s41598-019-44578-5 |
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author | Bashir, Khalid Kappala, Deepthi Singh, Yogendra Dar, Javeed Ahmad Mariappan, Asok Kumar Kumar, Ajay Krishnaswamy, Narayanan Dey, Sohini Chellappa, Madhan Mohan Goswami, Tapas Kumar Gupta, Vivek Kumar Ramakrishnan, Saravanan |
author_facet | Bashir, Khalid Kappala, Deepthi Singh, Yogendra Dar, Javeed Ahmad Mariappan, Asok Kumar Kumar, Ajay Krishnaswamy, Narayanan Dey, Sohini Chellappa, Madhan Mohan Goswami, Tapas Kumar Gupta, Vivek Kumar Ramakrishnan, Saravanan |
author_sort | Bashir, Khalid |
collection | PubMed |
description | Live intermediate plus infectious bursal disease virus (IBDV) vaccines (hot vaccines) are used for protection against the virulent IBDV strains in young chickens. We evaluated the potential of Toll-like receptor (TLR) agonists to alleviate hot vaccine-induced immunosuppression. The combination of Pam3CSK4 and poly I:C synergistically upregulated IFN-β, IFN-γ, IL-12, IL-4, and IL-13 transcripts and cross-inhibited IL-1β, IL-10, and iNOS transcripts in the chicken peripheral blood mononuclear cells (PBMCs) as analyzed by quantitative real-time PCR. Further, four-week old specific pathogen free White Leghorn chickens (n = 60) were randomly divided into six groups and either immunized with hot IBDV vaccine with or without Pam3CSK4 and/or poly I:C or not vaccinated to serve as controls. The results indicated that poly I:C alone and in combination with Pam3CSK4 alleviated vaccine-induced immunosuppression, as evidenced by greater weight gain, increased overall antibody responses to both sheep erythrocytes and live infectious bronchitis virus vaccine, upregulated IFN-γ transcripts and nitric oxide production by PBMCs (P < 0.05), and lower bursal lesion score in the experimental birds. In conclusion, poly I:C alone and its combination with Pam3CSK4 reduced the destruction of B cells as well as bursal damage with restoration of function of T cells and macrophages when used with a hot IBDV vaccine. |
format | Online Article Text |
id | pubmed-6547722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65477222019-06-10 Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken Bashir, Khalid Kappala, Deepthi Singh, Yogendra Dar, Javeed Ahmad Mariappan, Asok Kumar Kumar, Ajay Krishnaswamy, Narayanan Dey, Sohini Chellappa, Madhan Mohan Goswami, Tapas Kumar Gupta, Vivek Kumar Ramakrishnan, Saravanan Sci Rep Article Live intermediate plus infectious bursal disease virus (IBDV) vaccines (hot vaccines) are used for protection against the virulent IBDV strains in young chickens. We evaluated the potential of Toll-like receptor (TLR) agonists to alleviate hot vaccine-induced immunosuppression. The combination of Pam3CSK4 and poly I:C synergistically upregulated IFN-β, IFN-γ, IL-12, IL-4, and IL-13 transcripts and cross-inhibited IL-1β, IL-10, and iNOS transcripts in the chicken peripheral blood mononuclear cells (PBMCs) as analyzed by quantitative real-time PCR. Further, four-week old specific pathogen free White Leghorn chickens (n = 60) were randomly divided into six groups and either immunized with hot IBDV vaccine with or without Pam3CSK4 and/or poly I:C or not vaccinated to serve as controls. The results indicated that poly I:C alone and in combination with Pam3CSK4 alleviated vaccine-induced immunosuppression, as evidenced by greater weight gain, increased overall antibody responses to both sheep erythrocytes and live infectious bronchitis virus vaccine, upregulated IFN-γ transcripts and nitric oxide production by PBMCs (P < 0.05), and lower bursal lesion score in the experimental birds. In conclusion, poly I:C alone and its combination with Pam3CSK4 reduced the destruction of B cells as well as bursal damage with restoration of function of T cells and macrophages when used with a hot IBDV vaccine. Nature Publishing Group UK 2019-06-03 /pmc/articles/PMC6547722/ /pubmed/31160675 http://dx.doi.org/10.1038/s41598-019-44578-5 Text en © The Author(s) 2019 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 Bashir, Khalid Kappala, Deepthi Singh, Yogendra Dar, Javeed Ahmad Mariappan, Asok Kumar Kumar, Ajay Krishnaswamy, Narayanan Dey, Sohini Chellappa, Madhan Mohan Goswami, Tapas Kumar Gupta, Vivek Kumar Ramakrishnan, Saravanan Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
title | Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
title_full | Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
title_fullStr | Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
title_full_unstemmed | Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
title_short | Combination of TLR2 and TLR3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
title_sort | combination of tlr2 and tlr3 agonists derepress infectious bursal disease virus vaccine-induced immunosuppression in the chicken |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547722/ https://www.ncbi.nlm.nih.gov/pubmed/31160675 http://dx.doi.org/10.1038/s41598-019-44578-5 |
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