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Comparative qualitative and quantitative analysis of scleroderma (systemic sclerosis) serologic immunoassays

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dc.contributor.author Picha, L en
dc.contributor.author Pakas, I en
dc.contributor.author Guialis, A en
dc.contributor.author Moutsopoulos, HM en
dc.contributor.author Vlachoyiannopoulos, PG en
dc.date.accessioned 2014-03-01T01:57:20Z
dc.date.available 2014-03-01T01:57:20Z
dc.date.issued 2008 en
dc.identifier.issn 0896-8411 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/28403
dc.subject Antigenic source en
dc.subject Autoantibodies en
dc.subject Immunoblot en
dc.subject Systemic sclerosis (scleroderma) en
dc.subject.classification Immunology en
dc.subject.other LINKED-IMMUNOSORBENT-ASSAY en
dc.subject.other TOPOISOMERASE-I SCL-70 en
dc.subject.other ANTICENTROMERE ANTIBODIES en
dc.subject.other ANTIHISTONE ANTIBODIES en
dc.subject.other CLINICAL ASSOCIATIONS en
dc.subject.other LUPUS-ERYTHEMATOSUS en
dc.subject.other RIBONUCLEOPROTEIN PARTICLE en
dc.subject.other PULMONARY-HYPERTENSION en
dc.subject.other POLYMYOSITIS OVERLAP en
dc.subject.other NUCLEOLAR ANTIBODIES en
dc.title Comparative qualitative and quantitative analysis of scleroderma (systemic sclerosis) serologic immunoassays en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2008 en
heal.abstract The heterogeneity of autoantibody specificities occurring in sera from patients with systemic sclerosis (SSc) raised the necessity of developing various methodologies for their detection. A cohort of 150 SSc patients were selected and tested by Indirect Immunofluorescence (IIF), Counterimmunoelectrophoresis (CIE), Immunoblot (IB) using various extracts as antigenic source and RNA precipitation. By preparing a nuclear (IB-nuclear) and a metaphase chromosomal-enriched extract (IB-MC-pellet) from HeLa cells as well as a nucleolar (IB-nucleolar) and a histone (IB-histone) extract from rat liver nuclei, we assessed their sensitivity and specificity for anti-Topo 1, anti-U3RNP, anti-H-1, anti-snRNPs antibodies and ACA. IB-nuclear revealed the highest frequency of anti-Topo I antibodies, while CIE, IB-nucleolar and IB-MC-pellet, when compared to IB-nuclear showed a sensitivity of 89%, 87% and 95%, respectively. IB-MC-pellet was unique for ACA recognition, while IB-nucleolar and IB-MC-pellet showed excellent sensitivity for anti-U3RNP and anti-H, antibody detection. We conclude that IB-nuclear is a highly sensitive system for anti Topo I antibodies determination, but CIE reveals a good sensitivity to be used as a first screening test. IB-nucleolar or IB-MC-pellet are important techniques to detect the variety of antibodies to nucleolus and chromatin-related constituents. A novel specificity against a 28 kD nucleolar protein, non-associated with RNAs is also presented. (C) 2008 Elsevier Ltd. All rights reserved. en
heal.publisher ACADEMIC PRESS LTD ELSEVIER SCIENCE LTD en
heal.journalName JOURNAL OF AUTOIMMUNITY en
dc.identifier.isi ISI:000259880700012 en
dc.identifier.volume 31 en
dc.identifier.issue 2 en
dc.identifier.spage 166 en
dc.identifier.epage 174 en


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