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Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs

Saponin-based adjuvants have been widely used to enhance humoral and cellular immune responses in many species, but their mode of action is not fully understood. A characterization of the porcine transcriptional response to Matrix-M was performed in vitro using lymphocytes, monocytes or monocyte-der...

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Autores principales: Ahlberg, Viktor, Hjertner, Bernt, Wallgren, Per, Hellman, Stina, Lövgren Bengtsson, Karin, Fossum, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441066/
https://www.ncbi.nlm.nih.gov/pubmed/28532492
http://dx.doi.org/10.1186/s13567-017-0437-2
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author Ahlberg, Viktor
Hjertner, Bernt
Wallgren, Per
Hellman, Stina
Lövgren Bengtsson, Karin
Fossum, Caroline
author_facet Ahlberg, Viktor
Hjertner, Bernt
Wallgren, Per
Hellman, Stina
Lövgren Bengtsson, Karin
Fossum, Caroline
author_sort Ahlberg, Viktor
collection PubMed
description Saponin-based adjuvants have been widely used to enhance humoral and cellular immune responses in many species, but their mode of action is not fully understood. A characterization of the porcine transcriptional response to Matrix-M was performed in vitro using lymphocytes, monocytes or monocyte-derived dendritic cells (MoDCs) and in vivo. The effect of Matrix-M was also evaluated in specific pathogen free (SPF) pigs exposed to conventionally reared pigs. The pro-inflammatory cytokine genes IL1B and CXCL8 were up-regulated in monocytes and lymphocytes after Matrix-M exposure. Matrix-M also induced IL12B, IL17A and IFNG in lymphocytes and IFN-α gene expression in MoDCs. Several genes were indicated as up-regulated by Matrix-M in blood 18 h after injection, of which the genes for IFN-α and TLR2 could be statistically confirmed. Respiratory disease developed in all SPF pigs mixed with conventional pigs within 1–3 days. Two out of four SPF pigs injected with saline prior to contact exposure displayed systemic symptoms that was not recorded for the four pigs administered Matrix-M. Granulocyte counts, serum amyloid A levels and transcription of IL18 and TLR2 coincided with disease progression in the pigs. These results support further evaluation of Matrix-M as a possible enhancer of innate immune responses during critical moments in pig management. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-017-0437-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-54410662017-05-24 Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs Ahlberg, Viktor Hjertner, Bernt Wallgren, Per Hellman, Stina Lövgren Bengtsson, Karin Fossum, Caroline Vet Res Research Article Saponin-based adjuvants have been widely used to enhance humoral and cellular immune responses in many species, but their mode of action is not fully understood. A characterization of the porcine transcriptional response to Matrix-M was performed in vitro using lymphocytes, monocytes or monocyte-derived dendritic cells (MoDCs) and in vivo. The effect of Matrix-M was also evaluated in specific pathogen free (SPF) pigs exposed to conventionally reared pigs. The pro-inflammatory cytokine genes IL1B and CXCL8 were up-regulated in monocytes and lymphocytes after Matrix-M exposure. Matrix-M also induced IL12B, IL17A and IFNG in lymphocytes and IFN-α gene expression in MoDCs. Several genes were indicated as up-regulated by Matrix-M in blood 18 h after injection, of which the genes for IFN-α and TLR2 could be statistically confirmed. Respiratory disease developed in all SPF pigs mixed with conventional pigs within 1–3 days. Two out of four SPF pigs injected with saline prior to contact exposure displayed systemic symptoms that was not recorded for the four pigs administered Matrix-M. Granulocyte counts, serum amyloid A levels and transcription of IL18 and TLR2 coincided with disease progression in the pigs. These results support further evaluation of Matrix-M as a possible enhancer of innate immune responses during critical moments in pig management. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-017-0437-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-22 2017 /pmc/articles/PMC5441066/ /pubmed/28532492 http://dx.doi.org/10.1186/s13567-017-0437-2 Text en © The Author(s) 2017 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 Article
Ahlberg, Viktor
Hjertner, Bernt
Wallgren, Per
Hellman, Stina
Lövgren Bengtsson, Karin
Fossum, Caroline
Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs
title Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs
title_full Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs
title_fullStr Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs
title_full_unstemmed Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs
title_short Innate immune responses induced by the saponin adjuvant Matrix-M in specific pathogen free pigs
title_sort innate immune responses induced by the saponin adjuvant matrix-m in specific pathogen free pigs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441066/
https://www.ncbi.nlm.nih.gov/pubmed/28532492
http://dx.doi.org/10.1186/s13567-017-0437-2
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