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Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study

INTRODUCTION: Anti-glomerular basement membrane (GBM) antibodies are pathogenic antibodies first detected in renal-limited anti-GBM disease and in Goodpasture disease, the latter characterized by rapidly progressive crescentic glomerulonephritis combined with intra-alveolar hemorrhage. Studies have...

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Autores principales: Bourse Chalvon, Nellie, Orquevaux, Pauline, Giusti, Delphine, Gatouillat, Gregory, Tabary, Thierry, Tonye Libyh, Marcelle, Chrusciel, Jan, Drame, Moustapha, Stockton-Bliard, Grace, Amoura, Zahir, Arnaud, Laurent, Lorenz, Hanns-Martin, Blaison, Gilles, Bonnotte, Bernard, Magy-Bertrand, Nadine, Revuz, Sabine, Voll, Reinhard Edmund, Hinschberger, Oliver, Schwarting, Andreas, Pham, Bach Nga, Martin, Thierry, Pennaforte, Jean-Loup, Servettaz, Amelie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768036/
https://www.ncbi.nlm.nih.gov/pubmed/33381119
http://dx.doi.org/10.3389/fimmu.2020.597863
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author Bourse Chalvon, Nellie
Orquevaux, Pauline
Giusti, Delphine
Gatouillat, Gregory
Tabary, Thierry
Tonye Libyh, Marcelle
Chrusciel, Jan
Drame, Moustapha
Stockton-Bliard, Grace
Amoura, Zahir
Arnaud, Laurent
Lorenz, Hanns-Martin
Blaison, Gilles
Bonnotte, Bernard
Magy-Bertrand, Nadine
Revuz, Sabine
Voll, Reinhard Edmund
Hinschberger, Oliver
Schwarting, Andreas
Pham, Bach Nga
Martin, Thierry
Pennaforte, Jean-Loup
Servettaz, Amelie
author_facet Bourse Chalvon, Nellie
Orquevaux, Pauline
Giusti, Delphine
Gatouillat, Gregory
Tabary, Thierry
Tonye Libyh, Marcelle
Chrusciel, Jan
Drame, Moustapha
Stockton-Bliard, Grace
Amoura, Zahir
Arnaud, Laurent
Lorenz, Hanns-Martin
Blaison, Gilles
Bonnotte, Bernard
Magy-Bertrand, Nadine
Revuz, Sabine
Voll, Reinhard Edmund
Hinschberger, Oliver
Schwarting, Andreas
Pham, Bach Nga
Martin, Thierry
Pennaforte, Jean-Loup
Servettaz, Amelie
author_sort Bourse Chalvon, Nellie
collection PubMed
description INTRODUCTION: Anti-glomerular basement membrane (GBM) antibodies are pathogenic antibodies first detected in renal-limited anti-GBM disease and in Goodpasture disease, the latter characterized by rapidly progressive crescentic glomerulonephritis combined with intra-alveolar hemorrhage. Studies have suggested that anti-GBM antibody positivity may be of interest in lupus nephritis (LN). Moreover, severe anti-GBM vasculitis cases in patients with systemic lupus erythematosus (SLE) have been described in the literature, but few studies have assessed the incidence of anti-GBM antibodies in SLE patients. OBJECTIVE: The main study objective was to determine if positive anti-GBM antibodies were present in the serum of SLE patients with or without proliferative renal damage and compared to a healthy control group. METHODOLOGY: This retrospective study was performed on SLE patients’ sera from a Franco-German European biobank, developed between 2011 and 2014, from 17 hospital centers in the Haut-Rhin region. Patients were selected according to their renal involvement, and matched by age and gender. The serum from healthy voluntary blood donors was also tested. Anti-GBM were screened by fluorescence enzyme immunoassay (FEIA), and then by indirect immunofluorescence (IIF) in case of low reactivity detection (titer >6 U/ml). RESULTS: The cohort was composed of 100 SLE patients with proliferative LN (27% with class III, 67% with class IV, and 6% with class V), compared to 100 SLE patients without LN and 100 controls. Patients were mostly Caucasian and met the ACR 1997 criteria and/or the SLICC 2012 criteria. Among the 300 tested sera, no significant levels of anti-GBM antibodies were detected (>10 U/ml) by the automated technique, three sera were found “ambivalent” (>7 U/ml): one in the SLE with LN group and two in the SLE without LN group. Subsequent IIF assays did not detect anti-GBM antibodies. CONCLUSION: Anti-GBM antibodies were not detected in the serum of Caucasian patients with SLE, even in case of renal involvement, a situation favoring the antigenic exposure of glomerular basement membranes. Our results reaffirm the central role of anti-GBM antibodies as a specific diagnostic biomarker for Goodpasture vasculitis and therefore confirm that anti-GBM antibody must not be carried out in patients with SLE (with or without LN) in the absence of disease-suggestive symptoms.
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spelling pubmed-77680362020-12-29 Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study Bourse Chalvon, Nellie Orquevaux, Pauline Giusti, Delphine Gatouillat, Gregory Tabary, Thierry Tonye Libyh, Marcelle Chrusciel, Jan Drame, Moustapha Stockton-Bliard, Grace Amoura, Zahir Arnaud, Laurent Lorenz, Hanns-Martin Blaison, Gilles Bonnotte, Bernard Magy-Bertrand, Nadine Revuz, Sabine Voll, Reinhard Edmund Hinschberger, Oliver Schwarting, Andreas Pham, Bach Nga Martin, Thierry Pennaforte, Jean-Loup Servettaz, Amelie Front Immunol Immunology INTRODUCTION: Anti-glomerular basement membrane (GBM) antibodies are pathogenic antibodies first detected in renal-limited anti-GBM disease and in Goodpasture disease, the latter characterized by rapidly progressive crescentic glomerulonephritis combined with intra-alveolar hemorrhage. Studies have suggested that anti-GBM antibody positivity may be of interest in lupus nephritis (LN). Moreover, severe anti-GBM vasculitis cases in patients with systemic lupus erythematosus (SLE) have been described in the literature, but few studies have assessed the incidence of anti-GBM antibodies in SLE patients. OBJECTIVE: The main study objective was to determine if positive anti-GBM antibodies were present in the serum of SLE patients with or without proliferative renal damage and compared to a healthy control group. METHODOLOGY: This retrospective study was performed on SLE patients’ sera from a Franco-German European biobank, developed between 2011 and 2014, from 17 hospital centers in the Haut-Rhin region. Patients were selected according to their renal involvement, and matched by age and gender. The serum from healthy voluntary blood donors was also tested. Anti-GBM were screened by fluorescence enzyme immunoassay (FEIA), and then by indirect immunofluorescence (IIF) in case of low reactivity detection (titer >6 U/ml). RESULTS: The cohort was composed of 100 SLE patients with proliferative LN (27% with class III, 67% with class IV, and 6% with class V), compared to 100 SLE patients without LN and 100 controls. Patients were mostly Caucasian and met the ACR 1997 criteria and/or the SLICC 2012 criteria. Among the 300 tested sera, no significant levels of anti-GBM antibodies were detected (>10 U/ml) by the automated technique, three sera were found “ambivalent” (>7 U/ml): one in the SLE with LN group and two in the SLE without LN group. Subsequent IIF assays did not detect anti-GBM antibodies. CONCLUSION: Anti-GBM antibodies were not detected in the serum of Caucasian patients with SLE, even in case of renal involvement, a situation favoring the antigenic exposure of glomerular basement membranes. Our results reaffirm the central role of anti-GBM antibodies as a specific diagnostic biomarker for Goodpasture vasculitis and therefore confirm that anti-GBM antibody must not be carried out in patients with SLE (with or without LN) in the absence of disease-suggestive symptoms. Frontiers Media S.A. 2020-12-14 /pmc/articles/PMC7768036/ /pubmed/33381119 http://dx.doi.org/10.3389/fimmu.2020.597863 Text en Copyright © 2020 Bourse Chalvon, Orquevaux, Giusti, Gatouillat, Tabary, Tonye Libyh, Chrusciel, Drame, Stockton-Bliard, Amoura, Arnaud, Lorenz, Blaison, Bonnotte, Magy-Bertrand, Revuz, Voll, Hinschberger, Schwarting, Pham, Martin, Pennaforte and Servettaz http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bourse Chalvon, Nellie
Orquevaux, Pauline
Giusti, Delphine
Gatouillat, Gregory
Tabary, Thierry
Tonye Libyh, Marcelle
Chrusciel, Jan
Drame, Moustapha
Stockton-Bliard, Grace
Amoura, Zahir
Arnaud, Laurent
Lorenz, Hanns-Martin
Blaison, Gilles
Bonnotte, Bernard
Magy-Bertrand, Nadine
Revuz, Sabine
Voll, Reinhard Edmund
Hinschberger, Oliver
Schwarting, Andreas
Pham, Bach Nga
Martin, Thierry
Pennaforte, Jean-Loup
Servettaz, Amelie
Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study
title Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study
title_full Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study
title_fullStr Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study
title_full_unstemmed Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study
title_short Absence of Anti-Glomerular Basement Membrane Antibodies in 200 Patients With Systemic Lupus Erythematosus With or Without Lupus Nephritis: Results of the GOODLUPUS Study
title_sort absence of anti-glomerular basement membrane antibodies in 200 patients with systemic lupus erythematosus with or without lupus nephritis: results of the goodlupus study
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768036/
https://www.ncbi.nlm.nih.gov/pubmed/33381119
http://dx.doi.org/10.3389/fimmu.2020.597863
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