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cells, patients, article, arthritis, spa, google, scholar, pubmed, analysis, cas, staining, antibody, frequency, stimulation, study, peripheral, joints, hpf, figure, controls, spondylitis, cell, data, facet, compared, ankylosing, neutrophils, rheumatoid, inflammatory, rheum, spondyloarthritis, germany, ccr, higher, mncs, mpo, cdil, response, analysed, results, diseases, mast, immune, healthy, significantly, group, elisa, berlin, clone, authors,

Topics {✒️}

hla-b27/human β2-microglobulin-transgenic rats australo-anglo-american spondylitis consortium b27/β2-microglobulin-transgenic rats t-cell-derived growth factor open-label pilot study polyclonal anti-il-17a antibody anti-cd56 monoclonal antibody anti-glucocortin monoclonal antibody lipopolysaccharide-induced airway neutrophilia anti-cd56 antibody directed t-cell-driven disease [1] t-cell surface markers anti-il-17 antibody secukinumab rabbit anti-human myeloperoxidase anti-cd20 antibody directed t-cell-derived il-17 article download pdf hla-b27-restricted cd8+ phorbol 12-myristate 13-acetate/ionomycin anti-il-17a antibody t-cell response il-17-producing cell type including psoriatic arthritis van der linden detect il-17-expressing cells paraffin-embedded zygapophyseal joints discontinued adalimumab therapy t-cell responses related subjects kidney reperfusion injury il-17-secreting mononuclear cells il-17a producing cells full access 10 μg/ml brefeldin innate immune response privacy choices/manage cookies phorbol 12-myristate 13-acetate staphylococcus aureus enterotoxin published recently investigating isotype control antibody t-cell stimulation van der heijde il23 differentially regulates fully human antibody 1 μg/ml ionomycin asymmetrical arthritis predominantly il-17-producing neutrophils participated authors’ original file th1/th17 balance european economic area

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         headline:Analysis of IL-17+cells in facet joints of patients with spondyloarthritis suggests that the innate immune pathway might be of greater relevance than the Th17-mediated adaptive immune response
         description:In this study, we analysed the number of IL-17+ cells in facet joints, in the peripheral blood (PB) and synovial fluid (SF) of spondyloarthritis (SpA) patients and compared these results with those of patients with other rheumatic diseases and controls. Immunohistochemical analysis of IL-17+ cells was performed in facet joints of 33 ankylosing spondylitis (AS) patients and compared with data from 20 osteoarthritis (OA) patients. The frequency of IL-17+CD4+ T cells in PB and SF of SpA patients (PB n = 30, SF n = 11), rheumatoid arthritis (RA) patients (PB n = 14, SF n = 7), OA patients (PB n = 10) and healthy controls (PB n = 12) was analysed after stimulation with Staphylococcus aureus Enterotoxin B and phorbol 12-myristate 13-acetate/ionomycin and quantified by flow cytometry. In AS facet joints, the frequency of IL-17-secreting cells was significantly higher than in samples obtained from OA patients (P < 0.001), with a slight predominance of IL-17+ cells among the mononuclear cells (61.5% ± 14.9%) compared to cells with polysegmental nuclei. Immunofluorescence microscopy revealed that the majority of IL-17+ cells were myeloperoxidase-positive (35.84 ± 13.06/high-power field (HPF) and CD15+ neutrophils (24.25 ± 10.36/HPF), while CD3+ T cells (0.51 ± 0.49/HPF) and AA-1+ mast cells (2.28 ± 1.96/HPF) were less often IL-17-positive. The frequency of IL-17+CD4+ T cells in the PB and SF of SpA patients did not differ significantly compared to RA patients, OA patients or healthy controls. Our data suggest an important role for IL-17 in the inflammatory processes in AS. However, the innate immune pathway might be of greater relevance than the Th17-mediated adaptive immune response.
         datePublished:2011-06-20T00:00:00Z
         dateModified:2011-06-20T00:00:00Z
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            Ankylose Spondylitis
            Synovial Fluid
            Th17 Cell
            Facet Joint
            Rheumatology
            Orthopedics
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      headline:Analysis of IL-17+cells in facet joints of patients with spondyloarthritis suggests that the innate immune pathway might be of greater relevance than the Th17-mediated adaptive immune response
      description:In this study, we analysed the number of IL-17+ cells in facet joints, in the peripheral blood (PB) and synovial fluid (SF) of spondyloarthritis (SpA) patients and compared these results with those of patients with other rheumatic diseases and controls. Immunohistochemical analysis of IL-17+ cells was performed in facet joints of 33 ankylosing spondylitis (AS) patients and compared with data from 20 osteoarthritis (OA) patients. The frequency of IL-17+CD4+ T cells in PB and SF of SpA patients (PB n = 30, SF n = 11), rheumatoid arthritis (RA) patients (PB n = 14, SF n = 7), OA patients (PB n = 10) and healthy controls (PB n = 12) was analysed after stimulation with Staphylococcus aureus Enterotoxin B and phorbol 12-myristate 13-acetate/ionomycin and quantified by flow cytometry. In AS facet joints, the frequency of IL-17-secreting cells was significantly higher than in samples obtained from OA patients (P < 0.001), with a slight predominance of IL-17+ cells among the mononuclear cells (61.5% ± 14.9%) compared to cells with polysegmental nuclei. Immunofluorescence microscopy revealed that the majority of IL-17+ cells were myeloperoxidase-positive (35.84 ± 13.06/high-power field (HPF) and CD15+ neutrophils (24.25 ± 10.36/HPF), while CD3+ T cells (0.51 ± 0.49/HPF) and AA-1+ mast cells (2.28 ± 1.96/HPF) were less often IL-17-positive. The frequency of IL-17+CD4+ T cells in the PB and SF of SpA patients did not differ significantly compared to RA patients, OA patients or healthy controls. Our data suggest an important role for IL-17 in the inflammatory processes in AS. However, the innate immune pathway might be of greater relevance than the Th17-mediated adaptive immune response.
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      dateModified:2011-06-20T00:00:00Z
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         Rheumatoid Arthritis Patient
         Ankylose Spondylitis
         Synovial Fluid
         Th17 Cell
         Facet Joint
         Rheumatology
         Orthopedics
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      name:Department of Gastroenterology, Infectiology and Rheumatology, Charité Berlin, Berlin, Germany
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