Cargando…

The effect of CpG-ODN on antigen presenting cells of the foal

BACKGROUND: Cytosine-phosphate-guanosine oligodeoxynucleotide (CpG-ODN) has been used successfully to induce immune responses against viral and intracellular organisms in mammals. The main objective of this study was to test the effect of CpG-ODN on antigen presenting cells of young foals. METHODS:...

Descripción completa

Detalles Bibliográficos
Autores principales: Flaminio, M Julia BF, Borges, Alexandre S, Nydam, Daryl V, Horohov, David W, Hecker, Rolf, Matychak, Mary Beth
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797044/
https://www.ncbi.nlm.nih.gov/pubmed/17254326
http://dx.doi.org/10.1186/1476-8518-5-1
_version_ 1782132291722543104
author Flaminio, M Julia BF
Borges, Alexandre S
Nydam, Daryl V
Horohov, David W
Hecker, Rolf
Matychak, Mary Beth
author_facet Flaminio, M Julia BF
Borges, Alexandre S
Nydam, Daryl V
Horohov, David W
Hecker, Rolf
Matychak, Mary Beth
author_sort Flaminio, M Julia BF
collection PubMed
description BACKGROUND: Cytosine-phosphate-guanosine oligodeoxynucleotide (CpG-ODN) has been used successfully to induce immune responses against viral and intracellular organisms in mammals. The main objective of this study was to test the effect of CpG-ODN on antigen presenting cells of young foals. METHODS: Peripheral blood monocytes of foals (n = 7) were isolated in the first day of life and monthly thereafter up to 3 months of life. Adult horse (n = 7) monocytes were isolated and tested once for comparison. Isolated monocytes were stimulated with IL-4 and GM-CSF (to obtain dendritic cells, DC) or not stimulated (to obtain macrophages). Macrophages and DCs were stimulated for 14–16 hours with either CpG-ODN, LPS or not stimulated. The stimulated and non-stimulated cells were tested for cell surface markers (CD86 and MHC class II) using flow cytometry, mRNA expression of cytokines (IL-12, IFNα, IL-10) and TLR-9 using real time quantitative RT-PCR, and for the activation of the transcription factor NF-κB p65 using a chemiluminescence assay. RESULTS: The median fluorescence of the MHC class II molecule in non-stimulated foal macrophages and DCs at birth were 12.5 times and 11.2 times inferior, respectively, than adult horse cells (p = 0.009). That difference subsided at 3 months of life (p = 0.3). The expression of the CD86 co-stimulatory molecule was comparable in adult horse and foal macrophages and DCs, independent of treatment. CpG-ODN stimulation induced IL-12p40 (53 times) and IFNα (23 times) mRNA expression in CpG-ODN-treated adult horse DCs (p = 0.078), but not macrophages, in comparison to non-stimulated cells. In contrast, foal APCs did not respond to CpG-ODN stimulation with increased cytokine mRNA expression up to 3 months of age. TLR-9 mRNA expression and NF-kB activation (NF-kB p65) in foal DCs and macrophages were comparable (p > 0.05) to adult horse cells. CONCLUSION: CpG-ODN treatment did not induce specific maturation and cytokine expression in foal macrophages and DCs. Nevertheless, adult horse DCs, but not macrophages, increased their expression of IL-12 and IFNα cytokines upon CpG-ODN stimulation. Importantly, foals presented an age-dependent limitation in the expression of MHC class II in macrophages and DCs, independent of treatment.
format Text
id pubmed-1797044
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-17970442007-02-13 The effect of CpG-ODN on antigen presenting cells of the foal Flaminio, M Julia BF Borges, Alexandre S Nydam, Daryl V Horohov, David W Hecker, Rolf Matychak, Mary Beth J Immune Based Ther Vaccines Original Research BACKGROUND: Cytosine-phosphate-guanosine oligodeoxynucleotide (CpG-ODN) has been used successfully to induce immune responses against viral and intracellular organisms in mammals. The main objective of this study was to test the effect of CpG-ODN on antigen presenting cells of young foals. METHODS: Peripheral blood monocytes of foals (n = 7) were isolated in the first day of life and monthly thereafter up to 3 months of life. Adult horse (n = 7) monocytes were isolated and tested once for comparison. Isolated monocytes were stimulated with IL-4 and GM-CSF (to obtain dendritic cells, DC) or not stimulated (to obtain macrophages). Macrophages and DCs were stimulated for 14–16 hours with either CpG-ODN, LPS or not stimulated. The stimulated and non-stimulated cells were tested for cell surface markers (CD86 and MHC class II) using flow cytometry, mRNA expression of cytokines (IL-12, IFNα, IL-10) and TLR-9 using real time quantitative RT-PCR, and for the activation of the transcription factor NF-κB p65 using a chemiluminescence assay. RESULTS: The median fluorescence of the MHC class II molecule in non-stimulated foal macrophages and DCs at birth were 12.5 times and 11.2 times inferior, respectively, than adult horse cells (p = 0.009). That difference subsided at 3 months of life (p = 0.3). The expression of the CD86 co-stimulatory molecule was comparable in adult horse and foal macrophages and DCs, independent of treatment. CpG-ODN stimulation induced IL-12p40 (53 times) and IFNα (23 times) mRNA expression in CpG-ODN-treated adult horse DCs (p = 0.078), but not macrophages, in comparison to non-stimulated cells. In contrast, foal APCs did not respond to CpG-ODN stimulation with increased cytokine mRNA expression up to 3 months of age. TLR-9 mRNA expression and NF-kB activation (NF-kB p65) in foal DCs and macrophages were comparable (p > 0.05) to adult horse cells. CONCLUSION: CpG-ODN treatment did not induce specific maturation and cytokine expression in foal macrophages and DCs. Nevertheless, adult horse DCs, but not macrophages, increased their expression of IL-12 and IFNα cytokines upon CpG-ODN stimulation. Importantly, foals presented an age-dependent limitation in the expression of MHC class II in macrophages and DCs, independent of treatment. BioMed Central 2007-01-25 /pmc/articles/PMC1797044/ /pubmed/17254326 http://dx.doi.org/10.1186/1476-8518-5-1 Text en Copyright © 2007 Flaminio et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Flaminio, M Julia BF
Borges, Alexandre S
Nydam, Daryl V
Horohov, David W
Hecker, Rolf
Matychak, Mary Beth
The effect of CpG-ODN on antigen presenting cells of the foal
title The effect of CpG-ODN on antigen presenting cells of the foal
title_full The effect of CpG-ODN on antigen presenting cells of the foal
title_fullStr The effect of CpG-ODN on antigen presenting cells of the foal
title_full_unstemmed The effect of CpG-ODN on antigen presenting cells of the foal
title_short The effect of CpG-ODN on antigen presenting cells of the foal
title_sort effect of cpg-odn on antigen presenting cells of the foal
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797044/
https://www.ncbi.nlm.nih.gov/pubmed/17254326
http://dx.doi.org/10.1186/1476-8518-5-1
work_keys_str_mv AT flaminiomjuliabf theeffectofcpgodnonantigenpresentingcellsofthefoal
AT borgesalexandres theeffectofcpgodnonantigenpresentingcellsofthefoal
AT nydamdarylv theeffectofcpgodnonantigenpresentingcellsofthefoal
AT horohovdavidw theeffectofcpgodnonantigenpresentingcellsofthefoal
AT heckerrolf theeffectofcpgodnonantigenpresentingcellsofthefoal
AT matychakmarybeth theeffectofcpgodnonantigenpresentingcellsofthefoal
AT flaminiomjuliabf effectofcpgodnonantigenpresentingcellsofthefoal
AT borgesalexandres effectofcpgodnonantigenpresentingcellsofthefoal
AT nydamdarylv effectofcpgodnonantigenpresentingcellsofthefoal
AT horohovdavidw effectofcpgodnonantigenpresentingcellsofthefoal
AT heckerrolf effectofcpgodnonantigenpresentingcellsofthefoal
AT matychakmarybeth effectofcpgodnonantigenpresentingcellsofthefoal