Prevalence of anti-histone antibodies, their clinical significance and correlation with other autoantibodies in a cohort of Italian scleroderma patients
Autor: | Marilina Tampoia, Gabriella Pucci, Giovanni Lapadula, Francesca Scaccia, Antonella Simpatico, Irene Fineschi, Mauro Galeazzi, Gabriella Morozzi, Alessandra Chialà, Francesca Bellisai |
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Rok vydání: | 2011 |
Předmět: |
medicine.medical_specialty
Immunology Population Gastroenterology Scleroderma Rheumatology Anti-histone antibodies Internal medicine Pulmonary fibrosis Prevalence medicine Clinical significance education education.field_of_study biology business.industry Autoantibody medicine.disease systemic sclerosis anti-histone antibodies prevalence Clinical manifestations Cohort biology.protein Systemic sclerosis Original Article Antibody business |
Zdroj: | Auto-Immunity Highlights |
ISSN: | 2038-3274 2038-0305 |
DOI: | 10.1007/s13317-011-0015-y |
Popis: | Purpose The aim of our study was to determine the prevalence, clinical significance of antibodies to individual histone components and to evaluate their correlation with other autoantibody specificities in a cohort of Italian SSc patients. Some authors, demonstrated high prevalence of anti-histone antibodies in Italian SSc patients, associated with cardiac and renal involvement, suggesting a prognostic value of these autoantibodies; however, these data need to be confirmed. Methods Serum from 112 adult SSc patients, classified as diffuse (dc) and limited cutaneous (lc) SSc subsets were analyzed for autoantibodies by indirect immunofluorescence, fluoroenzyme immunoassay and enzyme immunoassay. Results AHA were found in 13 patients (11.6%), nine with lcSSc and four with dcSSc. Among them, five patients were anti-Scl70+ and four were anti-CENP B+. The presence of AHA was not associated with multi-organ involvement or with diffuse subset, as already described. Anti-Scl70 was detected in 43% of patients, anti-CENP B in 32% and anti-RNA polymerase III in 7.1%. We confirmed the association between anti-Scl70 antibodies and pulmonary fibrosis (OR 15.75, p |
Databáze: | OpenAIRE |
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