IgA-antigliadin antibodies in IgA mesangial nephropathy (Berger's disease)
Circulating IgA-antigliadin antibodies were detected with enzyme linked immunosorbent assay (ELISA) in four of 121 patients (3%) who had IgA mesangial nephropathy and 14 of 17 children (82%) who had untreated coeliac disease. No positive cases were present in the 54 healthy subjects of the control g...
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Veröffentlicht in: | BMJ 1987-07, Vol.295 (6590), p.78-80 |
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description | Circulating IgA-antigliadin antibodies were detected with enzyme linked immunosorbent assay (ELISA) in four of 121 patients (3%) who had IgA mesangial nephropathy and 14 of 17 children (82%) who had untreated coeliac disease. No positive cases were present in the 54 healthy subjects of the control group. Three patients who had IgA nephropathy and IgA-antigliadin antibodies underwent jejunal biopsy, and two showed mucosal atrophy. In these two patients urinary abnormalities, together with the IgA-antigliadin antibodies, disappeared completely after three months and five months, respectively, of following a gluten free diet. Circulating IgA immune complexes were found in most patients who had coeliac disease and Berger's disease associated with IgA-antigliadin antibodies, suggesting overactivity of the B cells producing IgA in both conditions. By contrast, a circulating IgA rheumatoid factor was detectable in three of the four patients who had IgA nephropathy and asymptomatic coeliac disease but was always absent in children who had coeliac disease but did not show signs of renal disease. These results suggest that a more complex abnormality in the IgA immune response is necessary for renal disease to become manifest in patients who have gluten enteropathy. |
doi_str_mv | 10.1136/bmj.295.6590.78 |
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No positive cases were present in the 54 healthy subjects of the control group. Three patients who had IgA nephropathy and IgA-antigliadin antibodies underwent jejunal biopsy, and two showed mucosal atrophy. In these two patients urinary abnormalities, together with the IgA-antigliadin antibodies, disappeared completely after three months and five months, respectively, of following a gluten free diet. Circulating IgA immune complexes were found in most patients who had coeliac disease and Berger's disease associated with IgA-antigliadin antibodies, suggesting overactivity of the B cells producing IgA in both conditions. By contrast, a circulating IgA rheumatoid factor was detectable in three of the four patients who had IgA nephropathy and asymptomatic coeliac disease but was always absent in children who had coeliac disease but did not show signs of renal disease. These results suggest that a more complex abnormality in the IgA immune response is necessary for renal disease to become manifest in patients who have gluten enteropathy.</description><identifier>ISSN: 0267-0623</identifier><identifier>ISSN: 0959-8138</identifier><identifier>EISSN: 1468-5833</identifier><identifier>DOI: 10.1136/bmj.295.6590.78</identifier><identifier>PMID: 3113643</identifier><language>eng</language><publisher>England: British Medical Journal Publishing Group</publisher><subject>Adolescent ; Adult ; Aged ; Antibodies ; Antigen-Antibody Complex - analysis ; Antigens ; Biopsies ; Celiac disease ; Celiac Disease - immunology ; Child ; Clinical Research ; Disease manifestations ; Female ; Gliadin - immunology ; Glomerulonephritis ; Glomerulonephritis, IGA - immunology ; Humans ; IgA glomerulonephritis ; Immune complex diseases ; Immunoglobulin A - analysis ; Jejunal diseases ; Kidney diseases ; Male ; Middle Aged ; Plant Proteins - immunology</subject><ispartof>BMJ, 1987-07, Vol.295 (6590), p.78-80</ispartof><rights>Copyright 1987 British Medical Journal</rights><rights>Copyright BMJ Publishing Group LTD Jul 11, 1987</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b542t-c401c1f9730ecd6aa5a5a157dbc73a5a183936c0eb6c3847831c5f21a2e433813</citedby><cites>FETCH-LOGICAL-b542t-c401c1f9730ecd6aa5a5a157dbc73a5a183936c0eb6c3847831c5f21a2e433813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/29527598$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/29527598$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3113643$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fornasieri, A</creatorcontrib><creatorcontrib>Sinico, R A</creatorcontrib><creatorcontrib>Maldifassi, P</creatorcontrib><creatorcontrib>Bernasconi, P</creatorcontrib><creatorcontrib>Vegni, M</creatorcontrib><creatorcontrib>D'Amico, G</creatorcontrib><title>IgA-antigliadin antibodies in IgA mesangial nephropathy (Berger's disease)</title><title>BMJ</title><addtitle>Br Med J (Clin Res Ed)</addtitle><description>Circulating IgA-antigliadin antibodies were detected with enzyme linked immunosorbent assay (ELISA) in four of 121 patients (3%) who had IgA mesangial nephropathy and 14 of 17 children (82%) who had untreated coeliac disease. No positive cases were present in the 54 healthy subjects of the control group. Three patients who had IgA nephropathy and IgA-antigliadin antibodies underwent jejunal biopsy, and two showed mucosal atrophy. In these two patients urinary abnormalities, together with the IgA-antigliadin antibodies, disappeared completely after three months and five months, respectively, of following a gluten free diet. Circulating IgA immune complexes were found in most patients who had coeliac disease and Berger's disease associated with IgA-antigliadin antibodies, suggesting overactivity of the B cells producing IgA in both conditions. By contrast, a circulating IgA rheumatoid factor was detectable in three of the four patients who had IgA nephropathy and asymptomatic coeliac disease but was always absent in children who had coeliac disease but did not show signs of renal disease. These results suggest that a more complex abnormality in the IgA immune response is necessary for renal disease to become manifest in patients who have gluten enteropathy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibodies</subject><subject>Antigen-Antibody Complex - analysis</subject><subject>Antigens</subject><subject>Biopsies</subject><subject>Celiac disease</subject><subject>Celiac Disease - immunology</subject><subject>Child</subject><subject>Clinical Research</subject><subject>Disease manifestations</subject><subject>Female</subject><subject>Gliadin - immunology</subject><subject>Glomerulonephritis</subject><subject>Glomerulonephritis, IGA - immunology</subject><subject>Humans</subject><subject>IgA glomerulonephritis</subject><subject>Immune complex diseases</subject><subject>Immunoglobulin A - analysis</subject><subject>Jejunal diseases</subject><subject>Kidney diseases</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Plant Proteins - immunology</subject><issn>0267-0623</issn><issn>0959-8138</issn><issn>1468-5833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkc2LFDEQxYMo6zDu2ZPQIOgq9Gy-k74I66DuyqII6mEvIZ2u6cnY3RmTnsX9700zw_hxWXJIhferR1UeQk8JXhDC5Hndbxa0EgspKrxQ-gGaES51KTRjD9EMU6lKLCl7jE5T2mCMKVO6kvwEnbCpn7MZ-njVXpR2GH3bedv4oZjqOjQeUpFfWS16SHZove2KAbbrGLZ2XN8VZ28hthBfpqLxCWyCV0_Qo5XtEpwe7jn69v7d1-Vlef35w9Xy4rqsBadj6TgmjqwqxTC4Rlor8iFCNbVTbCo1q5h0GGrpmOZKM-LEihJLgTOmCZujN3vf7a7uoXEwjNF2Zht9b-OdCdabf5XBr00bbg2hXFYSZ4MXB4MYfu4gjab3yUHX2QHCLhmlpMKkoveChOdZtVAZfP4fuAm7OORfMCS7cSVlxTN1vqdcDClFWB1nJthMgZgcqMmBmilQkzefo2d_r3rkD_H90TdpDPEoZwuqRDX1l3vdpxF-HXUbfxipmBLm0_el-bKU6kZf3piJf73np0HuG-43KMvA4g</recordid><startdate>19870711</startdate><enddate>19870711</enddate><creator>Fornasieri, A</creator><creator>Sinico, R A</creator><creator>Maldifassi, P</creator><creator>Bernasconi, P</creator><creator>Vegni, M</creator><creator>D'Amico, G</creator><general>British Medical Journal Publishing Group</general><general>British Medical Association</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19870711</creationdate><title>IgA-antigliadin antibodies in IgA mesangial nephropathy (Berger's disease)</title><author>Fornasieri, A ; 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No positive cases were present in the 54 healthy subjects of the control group. Three patients who had IgA nephropathy and IgA-antigliadin antibodies underwent jejunal biopsy, and two showed mucosal atrophy. In these two patients urinary abnormalities, together with the IgA-antigliadin antibodies, disappeared completely after three months and five months, respectively, of following a gluten free diet. Circulating IgA immune complexes were found in most patients who had coeliac disease and Berger's disease associated with IgA-antigliadin antibodies, suggesting overactivity of the B cells producing IgA in both conditions. By contrast, a circulating IgA rheumatoid factor was detectable in three of the four patients who had IgA nephropathy and asymptomatic coeliac disease but was always absent in children who had coeliac disease but did not show signs of renal disease. These results suggest that a more complex abnormality in the IgA immune response is necessary for renal disease to become manifest in patients who have gluten enteropathy.</abstract><cop>England</cop><pub>British Medical Journal Publishing Group</pub><pmid>3113643</pmid><doi>10.1136/bmj.295.6590.78</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antibodies Antigen-Antibody Complex - analysis Antigens Biopsies Celiac disease Celiac Disease - immunology Child Clinical Research Disease manifestations Female Gliadin - immunology Glomerulonephritis Glomerulonephritis, IGA - immunology Humans IgA glomerulonephritis Immune complex diseases Immunoglobulin A - analysis Jejunal diseases Kidney diseases Male Middle Aged Plant Proteins - immunology |
title | IgA-antigliadin antibodies in IgA mesangial nephropathy (Berger's disease) |
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