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Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus

INTRODUCTION: In this study, we sought to determine the diagnostic value and clinical laboratory associations of autoantibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in systemic lupus erythematosus (SLE). METHODS: Autoantibodies against recombinant ribos...

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Autores principales: Barkhudarova, Fidan, Dähnrich, Cornelia, Rosemann, Anke, Schneider, Udo, Stöcker, Winfried, Burmester, Gerd-Rüdiger, Egerer, Karl, Schlumberger, Wolfgang, Hiepe, Falk, Biesen, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241364/
https://www.ncbi.nlm.nih.gov/pubmed/21310064
http://dx.doi.org/10.1186/ar3244
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author Barkhudarova, Fidan
Dähnrich, Cornelia
Rosemann, Anke
Schneider, Udo
Stöcker, Winfried
Burmester, Gerd-Rüdiger
Egerer, Karl
Schlumberger, Wolfgang
Hiepe, Falk
Biesen, Robert
author_facet Barkhudarova, Fidan
Dähnrich, Cornelia
Rosemann, Anke
Schneider, Udo
Stöcker, Winfried
Burmester, Gerd-Rüdiger
Egerer, Karl
Schlumberger, Wolfgang
Hiepe, Falk
Biesen, Robert
author_sort Barkhudarova, Fidan
collection PubMed
description INTRODUCTION: In this study, we sought to determine the diagnostic value and clinical laboratory associations of autoantibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in systemic lupus erythematosus (SLE). METHODS: Autoantibodies against recombinant ribosomal P proteins (aRibP(R)0, aRibP(R)1 and aRibP(R)2) and antibodies against native ribosomal P heterocomplex (aRibP(N)H) were determined in sera from patients with SLE (n = 163), systemic sclerosis (n = 66), Sjögren's syndrome (n = 54), rheumatoid arthritis (n = 90) and healthy donors (n = 100) using enzyme-linked immunosorbent assay. Test results were correlated to medical records, including the American College of Rheumatology criteria, the Systemic Lupus Erythematosus Disease Activity Index 2000, laboratory data and medications of all SLE patients. RESULTS: Sensitivities of 22.0% for aRibP(R)0, 14.9% for aRibP(R)2, 14.3% for aRibP(N)H and 10.7% for aRibP(R)1 were obtained at a specificity of 99%. The assay for aRibP(R)0 detection demonstrated the best performance in receiver-operating characteristics analysis, with aRibP(R)0 detectable in 10% of anti-Smith antibody and anti-double-stranded DNA-negative sera at a specificity of 100%. ARibP(R)0 positivity was associated with lymphocytopenia. ARibP(R)1(+ )patients had significantly higher γ-glutamyl transpeptidase (GGT) levels than their aRibP(R)1(- )counterparts. No specific damage occurred in aRibP(+ )lupus patients compared with a group of age-, sex- and nephritis-matched aRibP(- )lupus patients within 3 years. CONCLUSIONS: The determination of antibodies against ribosomal P proteins improves the diagnosis of SLE and should therefore be implemented in upcoming criteria for the diagnosis or classification of SLE. High titers of aRibP(R)0 can be associated with lymphocytopenia, and high titers of aRibP(R)1 can be associated with elevated GGT levels. So far, there is no evidence for a prognostic value of aRibPs for damage.
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spelling pubmed-32413642011-12-17 Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus Barkhudarova, Fidan Dähnrich, Cornelia Rosemann, Anke Schneider, Udo Stöcker, Winfried Burmester, Gerd-Rüdiger Egerer, Karl Schlumberger, Wolfgang Hiepe, Falk Biesen, Robert Arthritis Res Ther Research Article INTRODUCTION: In this study, we sought to determine the diagnostic value and clinical laboratory associations of autoantibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in systemic lupus erythematosus (SLE). METHODS: Autoantibodies against recombinant ribosomal P proteins (aRibP(R)0, aRibP(R)1 and aRibP(R)2) and antibodies against native ribosomal P heterocomplex (aRibP(N)H) were determined in sera from patients with SLE (n = 163), systemic sclerosis (n = 66), Sjögren's syndrome (n = 54), rheumatoid arthritis (n = 90) and healthy donors (n = 100) using enzyme-linked immunosorbent assay. Test results were correlated to medical records, including the American College of Rheumatology criteria, the Systemic Lupus Erythematosus Disease Activity Index 2000, laboratory data and medications of all SLE patients. RESULTS: Sensitivities of 22.0% for aRibP(R)0, 14.9% for aRibP(R)2, 14.3% for aRibP(N)H and 10.7% for aRibP(R)1 were obtained at a specificity of 99%. The assay for aRibP(R)0 detection demonstrated the best performance in receiver-operating characteristics analysis, with aRibP(R)0 detectable in 10% of anti-Smith antibody and anti-double-stranded DNA-negative sera at a specificity of 100%. ARibP(R)0 positivity was associated with lymphocytopenia. ARibP(R)1(+ )patients had significantly higher γ-glutamyl transpeptidase (GGT) levels than their aRibP(R)1(- )counterparts. No specific damage occurred in aRibP(+ )lupus patients compared with a group of age-, sex- and nephritis-matched aRibP(- )lupus patients within 3 years. CONCLUSIONS: The determination of antibodies against ribosomal P proteins improves the diagnosis of SLE and should therefore be implemented in upcoming criteria for the diagnosis or classification of SLE. High titers of aRibP(R)0 can be associated with lymphocytopenia, and high titers of aRibP(R)1 can be associated with elevated GGT levels. So far, there is no evidence for a prognostic value of aRibPs for damage. BioMed Central 2011 2011-02-10 /pmc/articles/PMC3241364/ /pubmed/21310064 http://dx.doi.org/10.1186/ar3244 Text en Copyright ©2011 Barkhudarova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Barkhudarova, Fidan
Dähnrich, Cornelia
Rosemann, Anke
Schneider, Udo
Stöcker, Winfried
Burmester, Gerd-Rüdiger
Egerer, Karl
Schlumberger, Wolfgang
Hiepe, Falk
Biesen, Robert
Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus
title Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus
title_full Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus
title_fullStr Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus
title_full_unstemmed Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus
title_short Diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal P0, P1 and P2 proteins and their native heterocomplex in a Caucasian cohort with systemic lupus erythematosus
title_sort diagnostic value and clinical laboratory associations of antibodies against recombinant ribosomal p0, p1 and p2 proteins and their native heterocomplex in a caucasian cohort with systemic lupus erythematosus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241364/
https://www.ncbi.nlm.nih.gov/pubmed/21310064
http://dx.doi.org/10.1186/ar3244
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