New Coupled-Particle Light-Scattering Assay for Detection of Ro/SSA (52 and 60 Kilodaltons) and La/SSB Autoantibodies in Connective Tissue Diseases
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Published in | Clinical and Diagnostic Laboratory Immunology Vol. 8; no. 5; pp. 922 - 925 |
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Format | Journal Article |
Language | English |
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01.09.2001
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ISSN | 1556-6811 1071-412X 1556-679X 1098-6588 |
DOI | 10.1128/CDLI.8.5.922-925.2001 |
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AbstractList | The diagnostic and analytical performance of the coupled-particle light-scattering assay in detecting anti-Ro/SSA autoantibodies (the 60-kDa [Ro60] and the 52-kDa [Ro52] antibodies) and anti-La/SSB autoantibodies was evaluated. The antigens were obtained by recombinant DNA procedures to include the most immunogenic epitopes for each protein by using a prokaryotic expression system. Serum samples from 151 patients with connective tissue diseases and 52 control subjects (including patients with viral infections, patients with Lyme disease, and healthy subjects) were studied. Sensitivities for detection of anti-Ro/SSA and anti-La/SSB were 88.2 and 95.2%, respectively; specificities were 97.6 and 98.1%, respectively. The intra-assay coefficient of variation (CV) ranged from 4.3 to 10.9% for anti-Ro/SSA and from 2.8 to 12.5% for anti-La/SSB; interassay CVs ranged from 6.5 to 13.2% and from 8.2 to 14.5%, respectively. Among the anti-Ro/SSA-positive samples, Ro60 was recognized by 66% of the test sera and Ro52 was recognized by 95% of the test sera. Thirty-four percent of the Ro/SSA-positive sera were reactive only with the Ro52 antigen, indicating that anti-Ro52 is the most common antibody specificity recognized by anti-Ro/SSA autoantibodies. No differences were found between the prevalences of anti-Ro60 and anti-Ro52 in relation to systemic lupus erythematosus or Sjögren's syndrome. The results of the present study indicate that this new immunoassay is an efficient diagnostic tool for the detection of anti-Ro/SSA and anti-La/SSB antibodies in patients with autoimmune disorders. The diagnostic and analytical performance of the coupled-particle light-scattering assay in detecting anti-Ro/SSA autoantibodies (the 60-kDa [Ro60] and the 52-kDa [Ro52] antibodies) and anti-La/SSB autoantibodies was evaluated. The antigens were obtained by recombinant DNA procedures to include the most immunogenic epitopes for each protein by using a prokaryotic expression system. Serum samples from 151 patients with connective tissue diseases and 52 control subjects (including patients with viral infections, patients with Lyme disease, and healthy subjects) were studied. Sensitivities for detection of anti-Ro/SSA and anti-La/SSB were 88.2 and 95.2%, respectively; specificities were 97.6 and 98.1%, respectively. The intra-assay coefficient of variation (CV) ranged from 4.3 to 10.9% for anti-Ro/SSA and from 2.8 to 12.5% for anti-La/SSB; interassay CVs ranged from 6.5 to 13.2% and from 8.2 to 14.5%, respectively. Among the anti-Ro/SSA-positive samples, Ro60 was recognized by 66% of the test sera and Ro52 was recognized by 95% of the test sera. Thirty-four percent of the Ro/SSA-positive sera were reactive only with the Ro52 antigen, indicating that anti-Ro52 is the most common antibody specificity recognized by anti-Ro/SSA autoantibodies. No differences were found between the prevalences of anti-Ro60 and anti-Ro52 in relation to systemic lupus erythematosus or Sjögren's syndrome. The results of the present study indicate that this new immunoassay is an efficient diagnostic tool for the detection of anti-Ro/SSA and anti-La/SSB antibodies in patients with autoimmune disorders.The diagnostic and analytical performance of the coupled-particle light-scattering assay in detecting anti-Ro/SSA autoantibodies (the 60-kDa [Ro60] and the 52-kDa [Ro52] antibodies) and anti-La/SSB autoantibodies was evaluated. The antigens were obtained by recombinant DNA procedures to include the most immunogenic epitopes for each protein by using a prokaryotic expression system. Serum samples from 151 patients with connective tissue diseases and 52 control subjects (including patients with viral infections, patients with Lyme disease, and healthy subjects) were studied. Sensitivities for detection of anti-Ro/SSA and anti-La/SSB were 88.2 and 95.2%, respectively; specificities were 97.6 and 98.1%, respectively. The intra-assay coefficient of variation (CV) ranged from 4.3 to 10.9% for anti-Ro/SSA and from 2.8 to 12.5% for anti-La/SSB; interassay CVs ranged from 6.5 to 13.2% and from 8.2 to 14.5%, respectively. Among the anti-Ro/SSA-positive samples, Ro60 was recognized by 66% of the test sera and Ro52 was recognized by 95% of the test sera. Thirty-four percent of the Ro/SSA-positive sera were reactive only with the Ro52 antigen, indicating that anti-Ro52 is the most common antibody specificity recognized by anti-Ro/SSA autoantibodies. No differences were found between the prevalences of anti-Ro60 and anti-Ro52 in relation to systemic lupus erythematosus or Sjögren's syndrome. The results of the present study indicate that this new immunoassay is an efficient diagnostic tool for the detection of anti-Ro/SSA and anti-La/SSB antibodies in patients with autoimmune disorders. The diagnostic and analytical performance of the coupled-particle light-scattering assay in detecting anti-Ro/SSA autoantibodies (the 60-kDa [Ro60] and the 52-kDa [Ro52] antibodies) and anti-La/SSB autoantibodies was evaluated. The antigens were obtained by recombinant DNA procedures to include the most immunogenic epitopes for each protein by using a prokaryotic expression system. Serum samples from 151 patients with connective tissue diseases and 52 control subjects (including patients with viral infections, patients with Lyme disease, and healthy subjects) were studied. Sensitivities for detection of anti-Ro/SSA and anti-La/SSB were 88.2 and 95.2%, respectively; specificities were 97.6 and 98.1%, respectively. The intra-assay coefficient of variation (CV) ranged from 4.3 to 10.9% for anti-Ro/SSA and from 2.8 to 12.5% for anti-La/SSB; interassay CVs ranged from 6.5 to 13.2% and from 8.2 to 14.5%, respectively. Among the anti-Ro/SSA-positive samples, Ro60 was recognized by 66% of the test sera and Ro52 was recognized by 95% of the test sera. Thirty-four percent of the Ro/SSA-positive sera were reactive only with the Ro52 antigen, indicating that anti-Ro52 is the most common antibody specificity recognized by anti-Ro/SSA autoantibodies. No differences were found between the prevalences of anti-Ro60 and anti-Ro52 in relation to systemic lupus erythematosus or Sjoegren's syndrome. The results of the present study indicate that this new immunoassay is an efficient diagnostic tool for the detection of anti-Ro/SSA and anti-La/SSB antibodies in patients with autoimmune disorders. Classifications Services CVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue CVI About CVI Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy CVI RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 1556-6811 Online ISSN: 1556-679X Copyright © 2014 by the American Society for Microbiology. For an alternate route to CVI .asm.org, visit: CVI The diagnostic and analytical performance of the coupled-particle light-scattering assay in detecting anti-Ro/SSA autoantibodies (the 60-kDa [Ro60] and the 52-kDa [Ro52] antibodies) and anti-La/SSB autoantibodies was evaluated. The antigens were obtained by recombinant DNA procedures to include the most immunogenic epitopes for each protein by using a prokaryotic expression system. Serum samples from 151 patients with connective tissue diseases and 52 control subjects (including patients with viral infections, patients with Lyme disease, and healthy subjects) were studied. Sensitivities for detection of anti-Ro/SSA and anti-La/SSB were 88.2 and 95.2%, respectively; specificities were 97.6 and 98.1%, respectively. The intra-assay coefficient of variation (CV) ranged from 4.3 to 10.9% for anti-Ro/SSA and from 2.8 to 12.5% for anti-La/SSB; interassay CVs ranged from 6.5 to 13.2% and from 8.2 to 14.5%, respectively. Among the anti-Ro/SSA-positive samples, Ro60 was recognized by 66% of the test sera and Ro52 was recognized by 95% of the test sera. Thirty-four percent of the Ro/SSA-positive sera were reactive only with the Ro52 antigen, indicating that anti-Ro52 is the most common antibody specificity recognized by anti-Ro/SSA autoantibodies. No differences were found between the prevalences of anti-Ro60 and anti-Ro52 in relation to systemic lupus erythematosus or Sjögren's syndrome. The results of the present study indicate that this new immunoassay is an efficient diagnostic tool for the detection of anti-Ro/SSA and anti-La/SSB antibodies in patients with autoimmune disorders. |
Author | Danilo Villalta Fabrizio Bonelli Elio Tonutti Renato Tozzoli Nicola Bizzaro |
AuthorAffiliation | Laboratorio di Patologia Clinica, Ospedale Civile, S. Donà di Piave, 1 Diasorin srl, Saluggia, 2 Istituto di Chimica Clinica, Azienda Ospedaliera S. Maria della Misericordia, Udine, 3 Laboratorio Analisi Chimico-cliniche e Microbiologia, Ospedale Civile, Latisana, 4 and Laboratorio di Microbiologia e Immunologia, Azienda Ospedaliera S. Maria degli Angeli, Pordenone, 5 Italy |
AuthorAffiliation_xml | – name: Laboratorio di Patologia Clinica, Ospedale Civile, S. Donà di Piave, 1 Diasorin srl, Saluggia, 2 Istituto di Chimica Clinica, Azienda Ospedaliera S. Maria della Misericordia, Udine, 3 Laboratorio Analisi Chimico-cliniche e Microbiologia, Ospedale Civile, Latisana, 4 and Laboratorio di Microbiologia e Immunologia, Azienda Ospedaliera S. Maria degli Angeli, Pordenone, 5 Italy |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/11527804$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_immbio_2005_11_004 crossref_primary_10_1007_BF03256416 crossref_primary_10_1016_j_aca_2004_01_021 crossref_primary_10_23736_S1825_859X_20_00049_3 crossref_primary_10_1016_j_autrev_2007_01_005 crossref_primary_10_1191_0961203306lu2326oa crossref_primary_10_3389_fimmu_2019_00444 crossref_primary_10_1016_j_autrev_2008_07_032 crossref_primary_10_1016_S1773_035X_08_71577_6 crossref_primary_10_1002_cyto_a_21009 crossref_primary_10_1111_ijcp_13679 crossref_primary_10_1515_cclm_2012_0191 crossref_primary_10_1007_s13317_011_0018_8 |
Cites_doi | 10.1128/CDLI.7.3.436-443.2000 10.1016/S0022-1759(98)00140-9 10.1016/S0021-9258(19)81321-2 10.1006/clin.1998.4560 10.1093/rheumatology/32.6.449 10.1006/jaut.1999.0298 10.1111/j.1600-0897.1992.tb00810.x 10.1073/pnas.82.7.2115 10.1016/B978-044482383-0/50120-5 10.1016/B978-044482383-0/50121-7 10.1002/art.1780330307 10.1093/nar/19.22.6337 10.1002/jcla.1860090304 10.1016/0022-1759(90)90362-Y 10.1046/j.1365-2362.1996.186316.x 10.1177/000456329803500104 10.1111/j.1365-2249.1992.tb06874.x 10.1093/ajcp/108.4.406 10.1073/pnas.85.24.9479 10.1002/art.1780330502 10.1093/clinchem/39.4.561 10.1006/jaut.1994.1027 10.1136/ard.55.2.116 10.1002/1529-0131(199904)42:3<455::AID-ANR10>3.0.CO;2-3 10.1016/S0049-0172(95)80004-2 10.1016/0896-8411(89)90167-4 10.1111/j.1365-2249.1991.tb05780.x 10.1006/geno.1994.1664 |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Corresponding author. Mailing address: Laboratorio di Patologia Clinica, Ospedale Civile, Via N. Sauro, 25, 30027 S. Donà di Piave (VE), Italy. Phone: 0421–227570 or 0421–227586. Fax: 0421–227571. E-mail: nbizzaro@dacos.it. |
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SubjectTerms | Antibodies and Mediators of Immunity Antibodies, Antinuclear - blood Antibody Specificity Autoantibodies - blood Autoimmune Diseases - blood Connective Tissue - immunology Connective Tissue - pathology Connective Tissue Diseases - blood Connective Tissue Diseases - diagnosis Connective Tissue Diseases - immunology HeLa Cells Humans La(SSB) antigen Light Lupus Erythematosus, Systemic - blood Lupus Erythematosus, Systemic - diagnosis Lupus Erythematosus, Systemic - immunology Molecular Weight Reproducibility of Results Ro(SSA) antigen Scattering, Radiation Sensitivity and Specificity Sjogren's Syndrome - blood Sjogren's Syndrome - diagnosis Sjogren's Syndrome - immunology Tumor Cells, Cultured |
Title | New Coupled-Particle Light-Scattering Assay for Detection of Ro/SSA (52 and 60 Kilodaltons) and La/SSB Autoantibodies in Connective Tissue Diseases |
URI | http://cvi.asm.org/content/8/5/922.abstract https://www.ncbi.nlm.nih.gov/pubmed/11527804 https://www.proquest.com/docview/18106498 https://www.proquest.com/docview/71137035 https://pubmed.ncbi.nlm.nih.gov/PMC96172 |
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