An immunoenzymatic technique for the detection of antinuclear antibodies
In the present work, we propose, for the detection of the anti-nuclear antibodies (ANA) an immunoenzymatic test in simple sandwich in heterogeneous phase (ANA-EIA) allowing the screening of the antinuclear antibodies, and its assessment in comparison with the indirect immunofluorescent assay (IFA) f...
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Veröffentlicht in: | Annales de biologie clinique (Paris) 2000-11, Vol.58 (6), p.711-714 |
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creator | Meriche, H Meriche-Gadiri, S Ghaffor, M Abbadi, M C |
description | In the present work, we propose, for the detection of the anti-nuclear antibodies (ANA) an immunoenzymatic test in simple sandwich in heterogeneous phase (ANA-EIA) allowing the screening of the antinuclear antibodies, and its assessment in comparison with the indirect immunofluorescent assay (IFA) for 292 sera of patients affected by rheumatic diseases and 40 sera of individuals presenting no pathology. The ANA-EIA test proved to have a sensitivity of 97% and a specificity of 96%. Moreover, it gives a global concordance of 96.6% and a discordance of 3.4% compared to IFA. Also, the analysis of correlation between this test and IFA for the positive individual gives a very good concordance according to homogeneous, speckled and nucleolar aspects. On the other hand, the results obtained for cytoplasmic aspect (74%), although acceptable, needs to be confirmed a second time with a more important sampling. According to the results obtained, this test could have an interesting routine application in laboratory of immunopathology given its analytic characteristics similar to those of IFA, and its great easiness of realisation. |
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The ANA-EIA test proved to have a sensitivity of 97% and a specificity of 96%. Moreover, it gives a global concordance of 96.6% and a discordance of 3.4% compared to IFA. Also, the analysis of correlation between this test and IFA for the positive individual gives a very good concordance according to homogeneous, speckled and nucleolar aspects. On the other hand, the results obtained for cytoplasmic aspect (74%), although acceptable, needs to be confirmed a second time with a more important sampling. 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The ANA-EIA test proved to have a sensitivity of 97% and a specificity of 96%. Moreover, it gives a global concordance of 96.6% and a discordance of 3.4% compared to IFA. Also, the analysis of correlation between this test and IFA for the positive individual gives a very good concordance according to homogeneous, speckled and nucleolar aspects. On the other hand, the results obtained for cytoplasmic aspect (74%), although acceptable, needs to be confirmed a second time with a more important sampling. According to the results obtained, this test could have an interesting routine application in laboratory of immunopathology given its analytic characteristics similar to those of IFA, and its great easiness of realisation.</description><subject>Antibodies, Antinuclear - analysis</subject><subject>Autoimmune Diseases - diagnosis</subject><subject>Autoimmune Diseases - immunology</subject><subject>Connective Tissue Diseases - diagnosis</subject><subject>Connective Tissue Diseases - immunology</subject><subject>Data Interpretation, Statistical</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Humans</subject><subject>Immunoenzyme Techniques - methods</subject><subject>Indicators and Reagents</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><issn>0003-3898</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1jzFPwzAUhD2AaCn8BeSJLdJz7CT2WFVAkSqxdI9s51k1iu0QO0P59VRQpjudPp3ubsgaAHjFpZIrcp_zJwCrJed3ZMUYKMnabk3220h9CEtMGL_PQRdvaUF7iv5rQerSTMsJ6YCXrPgUaXJUx-LjYkfU8683afCYH8it02PGx6tuyPH15bjbV4ePt_fd9lBNjegqVM4oq0GJwVpohUHXSKOM6xqujdKoQXQSleCt44o5x4STLbQ4MATWWL4hz3-105wuC3Ppg88Wx1FHTEvuu1rwupFwAZ-u4GICDv00-6Dnc_9_nf8AOspVkA</recordid><startdate>200011</startdate><enddate>200011</enddate><creator>Meriche, H</creator><creator>Meriche-Gadiri, S</creator><creator>Ghaffor, M</creator><creator>Abbadi, M C</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200011</creationdate><title>An immunoenzymatic technique for the detection of antinuclear antibodies</title><author>Meriche, H ; Meriche-Gadiri, S ; Ghaffor, M ; Abbadi, M C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p547-e9fb9ca094dcc064bef58b9bf753ab9aea0478e9436f391ff14f8606ed1e015c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>fre</language><creationdate>2000</creationdate><topic>Antibodies, Antinuclear - analysis</topic><topic>Autoimmune Diseases - diagnosis</topic><topic>Autoimmune Diseases - immunology</topic><topic>Connective Tissue Diseases - diagnosis</topic><topic>Connective Tissue Diseases - immunology</topic><topic>Data Interpretation, Statistical</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Humans</topic><topic>Immunoenzyme Techniques - methods</topic><topic>Indicators and Reagents</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meriche, H</creatorcontrib><creatorcontrib>Meriche-Gadiri, S</creatorcontrib><creatorcontrib>Ghaffor, M</creatorcontrib><creatorcontrib>Abbadi, M C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Annales de biologie clinique (Paris)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meriche, H</au><au>Meriche-Gadiri, S</au><au>Ghaffor, M</au><au>Abbadi, M C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An immunoenzymatic technique for the detection of antinuclear antibodies</atitle><jtitle>Annales de biologie clinique (Paris)</jtitle><addtitle>Ann Biol Clin (Paris)</addtitle><date>2000-11</date><risdate>2000</risdate><volume>58</volume><issue>6</issue><spage>711</spage><epage>714</epage><pages>711-714</pages><issn>0003-3898</issn><abstract>In the present work, we propose, for the detection of the anti-nuclear antibodies (ANA) an immunoenzymatic test in simple sandwich in heterogeneous phase (ANA-EIA) allowing the screening of the antinuclear antibodies, and its assessment in comparison with the indirect immunofluorescent assay (IFA) for 292 sera of patients affected by rheumatic diseases and 40 sera of individuals presenting no pathology. The ANA-EIA test proved to have a sensitivity of 97% and a specificity of 96%. Moreover, it gives a global concordance of 96.6% and a discordance of 3.4% compared to IFA. Also, the analysis of correlation between this test and IFA for the positive individual gives a very good concordance according to homogeneous, speckled and nucleolar aspects. On the other hand, the results obtained for cytoplasmic aspect (74%), although acceptable, needs to be confirmed a second time with a more important sampling. According to the results obtained, this test could have an interesting routine application in laboratory of immunopathology given its analytic characteristics similar to those of IFA, and its great easiness of realisation.</abstract><cop>France</cop><pmid>11098167</pmid><tpages>4</tpages></addata></record> |
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subjects | Antibodies, Antinuclear - analysis Autoimmune Diseases - diagnosis Autoimmune Diseases - immunology Connective Tissue Diseases - diagnosis Connective Tissue Diseases - immunology Data Interpretation, Statistical Fluorescent Antibody Technique, Indirect Humans Immunoenzyme Techniques - methods Indicators and Reagents Reproducibility of Results Sensitivity and Specificity |
title | An immunoenzymatic technique for the detection of antinuclear antibodies |
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