Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE
To better define the relationships between circulating autoantibodies and renal involvement in systemic lupus erythematosus (SLE), antibodies to both dsDNA and soluble cellular antigens were detected in sera from a large series of SLE patients. Significantly higher dsDNA binding activities and lower...
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Veröffentlicht in: | Autoimmunity (Chur, Switzerland) Switzerland), 1990, Vol.7 (1), p.13-21 |
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creator | Asero, R. Banfi, G. Radelli, L. Origgi, L. Bertetti, E. Vanoli, M. Riboldi, P. |
description | To better define the relationships between circulating autoantibodies and renal involvement in systemic lupus erythematosus (SLE), antibodies to both dsDNA and soluble cellular antigens were detected in sera from a large series of SLE patients. Significantly higher dsDNA binding activities and lower complement levels at onset were found in patients with renal disease; however, this was uniquely due to subjects with diffuse or focal proliferative glomerulonephritis. Patients with membranous nephropathy (MGN) showed very low dsDNA binding activities (6/9 of them being negative for dsDNA antibodies) and normal mean C3 and C4 levels. A comparison between patients with proliferative nephritis and patients without renal involvement with high dsDNA binding activities revealed significantly lower complement levels in the former group. No significant difference was observed in the prevalence of antibodies to soluble cellular antigens between patients with or without renal disease; however, nRNP antibody was two-fold more frequent in patients with MGN than in all other subgroups. This study highlights the close relationship between concurrently high anti-dsDNA and low complement levels and proliferative glomerulonephritis in SLE, and suggests that subjects with MGN may represent a subgroup of SLE patients showing peculiar serological features. Different mechanisms possibly involved in the pathogenesis of MGN in SLE are discussed. |
doi_str_mv | 10.3109/08916939009041046 |
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Significantly higher dsDNA binding activities and lower complement levels at onset were found in patients with renal disease; however, this was uniquely due to subjects with diffuse or focal proliferative glomerulonephritis. Patients with membranous nephropathy (MGN) showed very low dsDNA binding activities (6/9 of them being negative for dsDNA antibodies) and normal mean C3 and C4 levels. A comparison between patients with proliferative nephritis and patients without renal involvement with high dsDNA binding activities revealed significantly lower complement levels in the former group. No significant difference was observed in the prevalence of antibodies to soluble cellular antigens between patients with or without renal disease; however, nRNP antibody was two-fold more frequent in patients with MGN than in all other subgroups. This study highlights the close relationship between concurrently high anti-dsDNA and low complement levels and proliferative glomerulonephritis in SLE, and suggests that subjects with MGN may represent a subgroup of SLE patients showing peculiar serological features. Different mechanisms possibly involved in the pathogenesis of MGN in SLE are discussed.</description><identifier>ISSN: 0891-6934</identifier><identifier>EISSN: 1607-842X</identifier><identifier>DOI: 10.3109/08916939009041046</identifier><identifier>PMID: 2103306</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Adolescent ; Adult ; Antibodies, Antinuclear - analysis ; Antigens - immunology ; Biopsy ; complement ; Complement C3 - analysis ; Complement C4 - analysis ; DNA - immunology ; dsDNA antibody ; Female ; glomerulonephritis ; Glomerulonephritis - immunology ; Glomerulonephritis, Membranous - immunology ; Humans ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - immunology ; Lupus Erythematosus, Systemic - pathology ; Male ; Middle Aged ; soluble cellular antigens ; Systemic lupus erythematosus</subject><ispartof>Autoimmunity (Chur, Switzerland), 1990, Vol.7 (1), p.13-21</ispartof><rights>1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1990</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-208e41b9c7040fa73457ffce682822f3800b705304b5df323c617b271a6408723</citedby><cites>FETCH-LOGICAL-c401t-208e41b9c7040fa73457ffce682822f3800b705304b5df323c617b271a6408723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/08916939009041046$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/08916939009041046$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,4024,27923,27924,27925,59647,60436,61221,61402</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2103306$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asero, R.</creatorcontrib><creatorcontrib>Banfi, G.</creatorcontrib><creatorcontrib>Radelli, L.</creatorcontrib><creatorcontrib>Origgi, L.</creatorcontrib><creatorcontrib>Bertetti, E.</creatorcontrib><creatorcontrib>Vanoli, M.</creatorcontrib><creatorcontrib>Riboldi, P.</creatorcontrib><title>Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE</title><title>Autoimmunity (Chur, Switzerland)</title><addtitle>Autoimmunity</addtitle><description>To better define the relationships between circulating autoantibodies and renal involvement in systemic lupus erythematosus (SLE), antibodies to both dsDNA and soluble cellular antigens were detected in sera from a large series of SLE patients. Significantly higher dsDNA binding activities and lower complement levels at onset were found in patients with renal disease; however, this was uniquely due to subjects with diffuse or focal proliferative glomerulonephritis. Patients with membranous nephropathy (MGN) showed very low dsDNA binding activities (6/9 of them being negative for dsDNA antibodies) and normal mean C3 and C4 levels. A comparison between patients with proliferative nephritis and patients without renal involvement with high dsDNA binding activities revealed significantly lower complement levels in the former group. No significant difference was observed in the prevalence of antibodies to soluble cellular antigens between patients with or without renal disease; however, nRNP antibody was two-fold more frequent in patients with MGN than in all other subgroups. This study highlights the close relationship between concurrently high anti-dsDNA and low complement levels and proliferative glomerulonephritis in SLE, and suggests that subjects with MGN may represent a subgroup of SLE patients showing peculiar serological features. Different mechanisms possibly involved in the pathogenesis of MGN in SLE are discussed.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antibodies, Antinuclear - analysis</subject><subject>Antigens - immunology</subject><subject>Biopsy</subject><subject>complement</subject><subject>Complement C3 - analysis</subject><subject>Complement C4 - analysis</subject><subject>DNA - immunology</subject><subject>dsDNA antibody</subject><subject>Female</subject><subject>glomerulonephritis</subject><subject>Glomerulonephritis - immunology</subject><subject>Glomerulonephritis, Membranous - immunology</subject><subject>Humans</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Erythematosus, Systemic - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>soluble cellular antigens</subject><subject>Systemic lupus erythematosus</subject><issn>0891-6934</issn><issn>1607-842X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd2KFDEQhYMo67j6AF4IufKutfIznW70Zp39EwYUV8G7Jt1d2c6STmaTNMO8gw-9PTuDIKJXRTjfOVWpIuQ1g3eCQf0eqpqVtagBapAMZPmELFgJqqgk__mULPZ6MQPyOXmR0h0AcFXKE3LCGQgB5YL8-oZOZxt8GuyGfsK8RfT0zGfbht5iojnQ89R7TbXv94-b4KbWIV2hc5PT8ZG9RZ8egWubcnDh1nbauR09R2M99vTKhRHj5ILHzRBttolaT7_OjdHnRLc2D_RmffGSPDPaJXx1rKfkx-XF99V1sf5y9Xl1ti46CSwXHCqUrK07BRKMVkIulTEdlhWvODeiAmgVLAXIdtkbwUVXMtVyxXQpoVJcnJK3h9xNDPcTptyMNnXzh7THMKWmAlEpKMUMsgPYxZBSRNNsoh113DUMmv0Fmr8uMHveHMOndsT-t-O48ln_eNCtNyGOehui65usdy5EE7XvbNpH_zv-wx_2AbXLQ6cjNndhin7e23-GewBWiqcG</recordid><startdate>1990</startdate><enddate>1990</enddate><creator>Asero, R.</creator><creator>Banfi, G.</creator><creator>Radelli, L.</creator><creator>Origgi, L.</creator><creator>Bertetti, E.</creator><creator>Vanoli, M.</creator><creator>Riboldi, P.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1990</creationdate><title>Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE</title><author>Asero, R. ; Banfi, G. ; Radelli, L. ; Origgi, L. ; Bertetti, E. ; Vanoli, M. ; Riboldi, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-208e41b9c7040fa73457ffce682822f3800b705304b5df323c617b271a6408723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antibodies, Antinuclear - analysis</topic><topic>Antigens - immunology</topic><topic>Biopsy</topic><topic>complement</topic><topic>Complement C3 - analysis</topic><topic>Complement C4 - analysis</topic><topic>DNA - immunology</topic><topic>dsDNA antibody</topic><topic>Female</topic><topic>glomerulonephritis</topic><topic>Glomerulonephritis - immunology</topic><topic>Glomerulonephritis, Membranous - immunology</topic><topic>Humans</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Erythematosus, Systemic - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>soluble cellular antigens</topic><topic>Systemic lupus erythematosus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asero, R.</creatorcontrib><creatorcontrib>Banfi, G.</creatorcontrib><creatorcontrib>Radelli, L.</creatorcontrib><creatorcontrib>Origgi, L.</creatorcontrib><creatorcontrib>Bertetti, E.</creatorcontrib><creatorcontrib>Vanoli, M.</creatorcontrib><creatorcontrib>Riboldi, P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Autoimmunity (Chur, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asero, R.</au><au>Banfi, G.</au><au>Radelli, L.</au><au>Origgi, L.</au><au>Bertetti, E.</au><au>Vanoli, M.</au><au>Riboldi, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE</atitle><jtitle>Autoimmunity (Chur, Switzerland)</jtitle><addtitle>Autoimmunity</addtitle><date>1990</date><risdate>1990</risdate><volume>7</volume><issue>1</issue><spage>13</spage><epage>21</epage><pages>13-21</pages><issn>0891-6934</issn><eissn>1607-842X</eissn><abstract>To better define the relationships between circulating autoantibodies and renal involvement in systemic lupus erythematosus (SLE), antibodies to both dsDNA and soluble cellular antigens were detected in sera from a large series of SLE patients. Significantly higher dsDNA binding activities and lower complement levels at onset were found in patients with renal disease; however, this was uniquely due to subjects with diffuse or focal proliferative glomerulonephritis. Patients with membranous nephropathy (MGN) showed very low dsDNA binding activities (6/9 of them being negative for dsDNA antibodies) and normal mean C3 and C4 levels. A comparison between patients with proliferative nephritis and patients without renal involvement with high dsDNA binding activities revealed significantly lower complement levels in the former group. No significant difference was observed in the prevalence of antibodies to soluble cellular antigens between patients with or without renal disease; however, nRNP antibody was two-fold more frequent in patients with MGN than in all other subgroups. This study highlights the close relationship between concurrently high anti-dsDNA and low complement levels and proliferative glomerulonephritis in SLE, and suggests that subjects with MGN may represent a subgroup of SLE patients showing peculiar serological features. Different mechanisms possibly involved in the pathogenesis of MGN in SLE are discussed.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>2103306</pmid><doi>10.3109/08916939009041046</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Antibodies, Antinuclear - analysis Antigens - immunology Biopsy complement Complement C3 - analysis Complement C4 - analysis DNA - immunology dsDNA antibody Female glomerulonephritis Glomerulonephritis - immunology Glomerulonephritis, Membranous - immunology Humans Lupus Erythematosus, Systemic - complications Lupus Erythematosus, Systemic - immunology Lupus Erythematosus, Systemic - pathology Male Middle Aged soluble cellular antigens Systemic lupus erythematosus |
title | Relationship Between Antibodies to Dsdna and to Soluble Cellular Antigens and Histologically Defined Glomerulonephritis in Patients with SLE |
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