Anti-endothelial cell antibodies are prevalent in juvenile idiopathic arthritis: implications for clinical disease course and pathogenesis
To determine the prevalence of anti-endothelial cell antibodies (AECA) in children with juvenile idiopathic arthritis (JIA) versus healthy control children. Twenty-eight children with active JIA were studied (ten each with polyarticular and oligoarticular disease, and eight with systemic onset disea...
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Veröffentlicht in: | Rheumatology international 2007-05, Vol.27 (7), p.655-660 |
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description | To determine the prevalence of anti-endothelial cell antibodies (AECA) in children with juvenile idiopathic arthritis (JIA) versus healthy control children. Twenty-eight children with active JIA were studied (ten each with polyarticular and oligoarticular disease, and eight with systemic onset disease). AECA were determined by a cell-based ELISA from samples obtained every 3 months over a 2 year period in each subject. These levels were compared against previously determined levels of von Willebrand factor antigen, fibrin d-dimer, and soluble forms of ICAM-1 and E-selectin, as well as clinical measures of disease activity. AECA were detected in 5/10 oligoarticular, 6/10 polyarticular, and 7/8 systemic JIA subjects and 0/14 controls. Mean levels of AECA were significantly higher in subjects with oligoarticular, and especially systemic disease as compared to polyarticular and control groups when analyzed by ANOVA. AECA are prevalent in JIA and are present more often and at higher levels in systemic disease. |
doi_str_mv | 10.1007/s00296-006-0276-3 |
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Twenty-eight children with active JIA were studied (ten each with polyarticular and oligoarticular disease, and eight with systemic onset disease). AECA were determined by a cell-based ELISA from samples obtained every 3 months over a 2 year period in each subject. These levels were compared against previously determined levels of von Willebrand factor antigen, fibrin d-dimer, and soluble forms of ICAM-1 and E-selectin, as well as clinical measures of disease activity. AECA were detected in 5/10 oligoarticular, 6/10 polyarticular, and 7/8 systemic JIA subjects and 0/14 controls. Mean levels of AECA were significantly higher in subjects with oligoarticular, and especially systemic disease as compared to polyarticular and control groups when analyzed by ANOVA. 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Twenty-eight children with active JIA were studied (ten each with polyarticular and oligoarticular disease, and eight with systemic onset disease). AECA were determined by a cell-based ELISA from samples obtained every 3 months over a 2 year period in each subject. These levels were compared against previously determined levels of von Willebrand factor antigen, fibrin d-dimer, and soluble forms of ICAM-1 and E-selectin, as well as clinical measures of disease activity. AECA were detected in 5/10 oligoarticular, 6/10 polyarticular, and 7/8 systemic JIA subjects and 0/14 controls. Mean levels of AECA were significantly higher in subjects with oligoarticular, and especially systemic disease as compared to polyarticular and control groups when analyzed by ANOVA. AECA are prevalent in JIA and are present more often and at higher levels in systemic disease.</description><subject>Adolescent</subject><subject>Antibody Specificity</subject><subject>Arthritis, Juvenile - epidemiology</subject><subject>Arthritis, Juvenile - immunology</subject><subject>Autoantibodies - blood</subject><subject>Autoantibodies - immunology</subject><subject>Biomarkers</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Drug therapy</subject><subject>Endothelial Cells - immunology</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Infant</subject><subject>Seroepidemiologic Studies</subject><issn>0172-8172</issn><issn>1437-160X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkU2LFDEQhoMou-O6P8CLBA97a81Hd6fH27K47sKCFwVvIR_VTg2ZpE3SC_4Ff7UZZkDwUFWkeN5KFS8hbzn7wBlTHwtjYjt2jLUQauzkC7LhvVQdH9mPl2TDuBLd1NIleV3KnrX3OLILcskVHwc2DRvy5zZW7CD6VHcQ0ATqIARqWtcmj1CoyUCXDM8mQKwUI92vzxAxAEWPaTF1h65BdZexYvlE8bAEdKZiioXOKVMXMLZGoB4LmALUpTW3YqKnR3n6CREKljfk1WxCgetzvSLf7z9_u3vonr5-eby7feqcFGPtJOuVnJXxvl0vxnmWFqwHBXYLbphkP089nzwbttbySTDDnZUglRFWGOhneUVuTnOXnH6tUKo-YDlebSKktWjF5HaSom_g-__Afds8tt301P4Q_SSHBvET5HIqJcOsl4wHk39rzvTRJX1ySTeX9NElLZvm3Xnwag_g_ynOtsi_fjaQ4A</recordid><startdate>200705</startdate><enddate>200705</enddate><creator>Bloom, Bradley J</creator><creator>Toyoda, Mieko</creator><creator>Petrosian, Anna</creator><creator>Jordan, Stanley</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200705</creationdate><title>Anti-endothelial cell antibodies are prevalent in juvenile idiopathic arthritis: implications for clinical disease course and pathogenesis</title><author>Bloom, Bradley J ; 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Twenty-eight children with active JIA were studied (ten each with polyarticular and oligoarticular disease, and eight with systemic onset disease). AECA were determined by a cell-based ELISA from samples obtained every 3 months over a 2 year period in each subject. These levels were compared against previously determined levels of von Willebrand factor antigen, fibrin d-dimer, and soluble forms of ICAM-1 and E-selectin, as well as clinical measures of disease activity. AECA were detected in 5/10 oligoarticular, 6/10 polyarticular, and 7/8 systemic JIA subjects and 0/14 controls. Mean levels of AECA were significantly higher in subjects with oligoarticular, and especially systemic disease as compared to polyarticular and control groups when analyzed by ANOVA. 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subjects | Adolescent Antibody Specificity Arthritis, Juvenile - epidemiology Arthritis, Juvenile - immunology Autoantibodies - blood Autoantibodies - immunology Biomarkers Child Child, Preschool Drug therapy Endothelial Cells - immunology Health risk assessment Humans Infant Seroepidemiologic Studies |
title | Anti-endothelial cell antibodies are prevalent in juvenile idiopathic arthritis: implications for clinical disease course and pathogenesis |
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