Platelet antibodies in idiopathic thrombocytopenic purpura

An immunofluorescence (IF) technique for the detection of antibodies was applied to idiopathic thrombocytopenic purpura (ITP). Serum platelet antibodies were found in thirteen out of twenty-two patients (59 percent) with active disease, but in only four out of fifteen patients (27 percent) who had a...

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Veröffentlicht in:Clinical and experimental immunology 1980-03, Vol.39 (3), p.645-651
Hauptverfasser: Veenhoven, W A, Van der Schans, G S, Nieweg, H O
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creator Veenhoven, W A
Van der Schans, G S
Nieweg, H O
description An immunofluorescence (IF) technique for the detection of antibodies was applied to idiopathic thrombocytopenic purpura (ITP). Serum platelet antibodies were found in thirteen out of twenty-two patients (59 percent) with active disease, but in only four out of fifteen patients (27 percent) who had attained remission. Direct tests for platelet-associated IgG were positive in 36 and 44 percent of these patients respectively. In two cases IgM was observed on the patients' platelet membranes. C3 was not detedted on patients' platelets. Platelet-associated IgG was also found in several other disorders and its occurrence is not therefore diagnostic of ITP. In addition, serum platelet antibodies do not indicate specifically ITP as they may also be due to previous isoimmunization. Antibodies in the sera of patients with ITP generally did not fix Clq and in most cases bound to platelets only in the presence of EDTA. In contrast, isoantibodies often fixed Clq and they had equal affinity for platelets suspended in ACD or EDTA plasma. This was confirmed by quantitative data on IgG binding by platelets obtained by measuring 125-I-labelled protein A uptake. The simplicity of the IF technique permits its routine application and the technique may give useful information with respect to the nature of the antibodies. It must, however, be considered of limited value in the diagnosis of ITP.
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Serum platelet antibodies were found in thirteen out of twenty-two patients (59 percent) with active disease, but in only four out of fifteen patients (27 percent) who had attained remission. Direct tests for platelet-associated IgG were positive in 36 and 44 percent of these patients respectively. In two cases IgM was observed on the patients' platelet membranes. C3 was not detedted on patients' platelets. Platelet-associated IgG was also found in several other disorders and its occurrence is not therefore diagnostic of ITP. In addition, serum platelet antibodies do not indicate specifically ITP as they may also be due to previous isoimmunization. Antibodies in the sera of patients with ITP generally did not fix Clq and in most cases bound to platelets only in the presence of EDTA. In contrast, isoantibodies often fixed Clq and they had equal affinity for platelets suspended in ACD or EDTA plasma. This was confirmed by quantitative data on IgG binding by platelets obtained by measuring 125-I-labelled protein A uptake. The simplicity of the IF technique permits its routine application and the technique may give useful information with respect to the nature of the antibodies. It must, however, be considered of limited value in the diagnosis of ITP.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>PMID: 6991171</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Antibodies - analysis ; Blood Platelets - immunology ; Female ; Fluorescent Antibody Technique ; Humans ; Immunoglobulin G - immunology ; Male ; Protein Binding ; Purpura, Thrombocytopenic - immunology ; Staphylococcal Protein A - immunology</subject><ispartof>Clinical and experimental immunology, 1980-03, Vol.39 (3), p.645-651</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538143/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538143/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6991171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Veenhoven, W A</creatorcontrib><creatorcontrib>Van der Schans, G S</creatorcontrib><creatorcontrib>Nieweg, H O</creatorcontrib><title>Platelet antibodies in idiopathic thrombocytopenic purpura</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>An immunofluorescence (IF) technique for the detection of antibodies was applied to idiopathic thrombocytopenic purpura (ITP). Serum platelet antibodies were found in thirteen out of twenty-two patients (59 percent) with active disease, but in only four out of fifteen patients (27 percent) who had attained remission. Direct tests for platelet-associated IgG were positive in 36 and 44 percent of these patients respectively. In two cases IgM was observed on the patients' platelet membranes. C3 was not detedted on patients' platelets. Platelet-associated IgG was also found in several other disorders and its occurrence is not therefore diagnostic of ITP. In addition, serum platelet antibodies do not indicate specifically ITP as they may also be due to previous isoimmunization. Antibodies in the sera of patients with ITP generally did not fix Clq and in most cases bound to platelets only in the presence of EDTA. In contrast, isoantibodies often fixed Clq and they had equal affinity for platelets suspended in ACD or EDTA plasma. This was confirmed by quantitative data on IgG binding by platelets obtained by measuring 125-I-labelled protein A uptake. The simplicity of the IF technique permits its routine application and the technique may give useful information with respect to the nature of the antibodies. It must, however, be considered of limited value in the diagnosis of ITP.</description><subject>Adult</subject><subject>Antibodies - analysis</subject><subject>Blood Platelets - immunology</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Humans</subject><subject>Immunoglobulin G - immunology</subject><subject>Male</subject><subject>Protein Binding</subject><subject>Purpura, Thrombocytopenic - immunology</subject><subject>Staphylococcal Protein A - immunology</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkElLxEAQhRtRxjj6E4ScvAXSS3rxIMjgBgN60HPTS8VpSdIx3RHm3xtwEIWCR71XfA_qCBWY8qYihKljVNR1rSqFa3aKzlL6WFbOOVmhFVcKY4ELdP3SmQwd5NIMOdjoA6QyDGXwIY4m74Ir826KvY1un-MIw2KM87SMOUcnrekSXBx0jd7u7143j9X2-eFpc7utRsJxrrytHXEtw84S6xUnFhyTzFriBRdEUrDKKuMbQUEKYNhIhVslwbSkkYrRNbr54Y6z7cE7GPJkOj1OoTfTXkcT9P9kCDv9Hr80bqjEjC6AqwNgip8zpKz7kBx0nRkgzkmLBhPJBFkOL_82_VYcvkW_AZE4aZ4</recordid><startdate>19800301</startdate><enddate>19800301</enddate><creator>Veenhoven, W A</creator><creator>Van der Schans, G S</creator><creator>Nieweg, H O</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19800301</creationdate><title>Platelet antibodies in idiopathic thrombocytopenic purpura</title><author>Veenhoven, W A ; Van der Schans, G S ; Nieweg, H O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p261t-db0c2cf41cb2bd962bec484bb2d767283eb9b9ad573e87e41a891f98eaf258943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Adult</topic><topic>Antibodies - analysis</topic><topic>Blood Platelets - immunology</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Humans</topic><topic>Immunoglobulin G - immunology</topic><topic>Male</topic><topic>Protein Binding</topic><topic>Purpura, Thrombocytopenic - immunology</topic><topic>Staphylococcal Protein A - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Veenhoven, W A</creatorcontrib><creatorcontrib>Van der Schans, G S</creatorcontrib><creatorcontrib>Nieweg, H O</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Veenhoven, W A</au><au>Van der Schans, G S</au><au>Nieweg, H O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Platelet antibodies in idiopathic thrombocytopenic purpura</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>1980-03-01</date><risdate>1980</risdate><volume>39</volume><issue>3</issue><spage>645</spage><epage>651</epage><pages>645-651</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><abstract>An immunofluorescence (IF) technique for the detection of antibodies was applied to idiopathic thrombocytopenic purpura (ITP). Serum platelet antibodies were found in thirteen out of twenty-two patients (59 percent) with active disease, but in only four out of fifteen patients (27 percent) who had attained remission. Direct tests for platelet-associated IgG were positive in 36 and 44 percent of these patients respectively. In two cases IgM was observed on the patients' platelet membranes. C3 was not detedted on patients' platelets. Platelet-associated IgG was also found in several other disorders and its occurrence is not therefore diagnostic of ITP. In addition, serum platelet antibodies do not indicate specifically ITP as they may also be due to previous isoimmunization. Antibodies in the sera of patients with ITP generally did not fix Clq and in most cases bound to platelets only in the presence of EDTA. In contrast, isoantibodies often fixed Clq and they had equal affinity for platelets suspended in ACD or EDTA plasma. This was confirmed by quantitative data on IgG binding by platelets obtained by measuring 125-I-labelled protein A uptake. The simplicity of the IF technique permits its routine application and the technique may give useful information with respect to the nature of the antibodies. It must, however, be considered of limited value in the diagnosis of ITP.</abstract><cop>England</cop><pmid>6991171</pmid><tpages>7</tpages></addata></record>
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subjects Adult
Antibodies - analysis
Blood Platelets - immunology
Female
Fluorescent Antibody Technique
Humans
Immunoglobulin G - immunology
Male
Protein Binding
Purpura, Thrombocytopenic - immunology
Staphylococcal Protein A - immunology
title Platelet antibodies in idiopathic thrombocytopenic purpura
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