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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/69542
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dc.contributor.authorJulia, M. Julia B.F.-
dc.contributor.authorBorges, Alexandre Secorun-
dc.contributor.authorNydam, Daryl V.-
dc.contributor.authorHorohov, David W.-
dc.contributor.authorHecker, Rolf-
dc.contributor.authorMatychak, Mary Beth-
dc.date.accessioned2014-05-27T11:22:25Z-
dc.date.accessioned2016-10-25T18:23:37Z-
dc.date.available2014-05-27T11:22:25Z-
dc.date.available2016-10-25T18:23:37Z-
dc.date.issued2007-03-01-
dc.identifierhttp://dx.doi.org/10.1186/1476-8518-5-1-
dc.identifier.citationJournal of Immune Based Therapies and Vaccines, v. 5.-
dc.identifier.issn1476-8518-
dc.identifier.urihttp://hdl.handle.net/11449/69542-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69542-
dc.description.abstractBackground: 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. © 2007 Flaminio et al; licensee BioMed Central Ltd.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectalpha interferon-
dc.subjectCD86 antigen-
dc.subjectcell surface marker-
dc.subjectCpG oligodeoxynucleotide-
dc.subjectcytokine-
dc.subjectgranulocyte macrophage colony stimulating factor-
dc.subjectimmunoglobulin enhancer binding protein-
dc.subjectinterleukin 10-
dc.subjectinterleukin 12-
dc.subjectinterleukin 4-
dc.subjectlipopolysaccharide-
dc.subjectmajor histocompatibility antigen class 2-
dc.subjectmessenger RNA-
dc.subjecttoll like receptor 9-
dc.subjectanimal cell-
dc.subjectantigen presenting cell-
dc.subjectcell isolation-
dc.subjectcell stimulation-
dc.subjectchemoluminescence-
dc.subjectcontrolled study-
dc.subjectdendritic cell-
dc.subjectflow cytometry-
dc.subjectfoal-
dc.subjectgene expression-
dc.subjecthorse-
dc.subjectmacrophage-
dc.subjectmonocyte-
dc.subjectnonhuman-
dc.subjectreverse transcription polymerase chain reaction-
dc.titleThe effect of CpG-ODN on antigen presenting cells of the foalen
dc.typeoutro-
dc.contributor.institutionCornell University-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversity of Kentucky-
dc.contributor.institutionQiagen GmbH-
dc.description.affiliationDepartment of Clinical Sciences College of Veterinary Medicine Cornell University, Ithaca, NY-
dc.description.affiliationDepartamento de Clinica Veterinaria Faculdade de Medicina Veterinaria e Zootecnia Universidade Estadual Paulista 'Julio de Mesquita Filho', UNESP-Campus de Botucatu, Botucatu, SP-
dc.description.affiliationDepartment of Population Medicine and Diagnostics Sciences College of Veterinary Medicine Cornell University, Ithaca, NY-
dc.description.affiliationDepartment of Veterinary Science Maxwell H. Gluck Equine Research Center University of Kentucky, Lexington, KY-
dc.description.affiliationQiagen GmbH, Hilden-
dc.description.affiliationUnespDepartamento de Clinica Veterinaria Faculdade de Medicina Veterinaria e Zootecnia Universidade Estadual Paulista 'Julio de Mesquita Filho', UNESP-Campus de Botucatu, Botucatu, SP-
dc.identifier.doi10.1186/1476-8518-5-1-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-33847190253.pdf-
dc.relation.ispartofJournal of Immune Based Therapies and Vaccines-
dc.identifier.scopus2-s2.0-33847190253-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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