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A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation

Anti-fibrillarin autoantibodies are useful for the diagnosis and prognosis of systemic sclerosis (SSc). Anti-fibrillarin produces a clumpy nucleolar pattern in indirect immunofluorescence assay on HEp-2 cells (HEp-2 IFA). Here we develop and validate a reliable cell-based anti-fibrillarin assay (Fib...

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Autores principales: Keppeke, Gerson Dierley, Satoh, Minoru, Kayser, Cristiane, Matos, Pedro, Hasegawa, Tomoko, Tanaka, Shin, Diogenes, Larissa, Amaral, Rogerio Quintiliano, Rodrigues, Silvia Helena, Andrade, Luis Eduardo Coelho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549361/
https://www.ncbi.nlm.nih.gov/pubmed/36225928
http://dx.doi.org/10.3389/fimmu.2022.1011110
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author Keppeke, Gerson Dierley
Satoh, Minoru
Kayser, Cristiane
Matos, Pedro
Hasegawa, Tomoko
Tanaka, Shin
Diogenes, Larissa
Amaral, Rogerio Quintiliano
Rodrigues, Silvia Helena
Andrade, Luis Eduardo Coelho
author_facet Keppeke, Gerson Dierley
Satoh, Minoru
Kayser, Cristiane
Matos, Pedro
Hasegawa, Tomoko
Tanaka, Shin
Diogenes, Larissa
Amaral, Rogerio Quintiliano
Rodrigues, Silvia Helena
Andrade, Luis Eduardo Coelho
author_sort Keppeke, Gerson Dierley
collection PubMed
description Anti-fibrillarin autoantibodies are useful for the diagnosis and prognosis of systemic sclerosis (SSc). Anti-fibrillarin produces a clumpy nucleolar pattern in indirect immunofluorescence assay on HEp-2 cells (HEp-2 IFA). Here we develop and validate a reliable cell-based anti-fibrillarin assay (Fibrillarin/CBA) for use in clinical diagnostic laboratories. A TransMembrane Signal was fused to the human fibrillarin gene (TMS-fibrillarin). HEp-2 cells overexpressing transgenic TMS-fibrillarin at the cytoplasmic membrane were used as IFA substrate in the Fibrillarin/CBA. Sixty-two serum samples with nucleolar pattern in the HEp-2 IFA (41 clumpy; 21 homogeneous/punctate) were tested for anti-fibrillarin using Fibrillarin/CBA, immunoprecipitation (IP), line-blot and ELISA. In addition, samples from 106 SSc-patients were evaluated with Fibrillarin/CBA and the results were correlated with disease phenotypes. Thirty-eight of 41 samples with the clumpy nucleolar pattern (92.7%) were positive in the Fibrillarin/CBA, while all 21 samples with other nucleolar patterns were negative. Fibrillarin/CBA results agreed 100% with IP results. Among the 38 Fibrillarin/CBA-positive samples, only 15 (39.5%) and 11 (29%) were positive for anti-fibrillarin in line-blot and ELISA, respectively. Higher frequency of diffuse cutaneous SSc (dcSSc) phenotype (72.7% vs 36.8%; p=0.022), cardiac involvement (36.4% vs 6.5%; p=0.001) and scleroderma renal crisis (18.2% vs 3.3% p = 0.028) was observed in SSc patients with positive compared to negative Fibrillarin/CBA result. Performance of Fibrillarin/CBA in the detection of anti-fibrillarin autoantibodies was comparable to the gold standard IP. Positive Fibrillarin/CBA results correlated with disease phenotypes known to be associated with anti-fibrillarin autoantibodies, underscoring the clinical validation of this novel assay.
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spelling pubmed-95493612022-10-11 A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation Keppeke, Gerson Dierley Satoh, Minoru Kayser, Cristiane Matos, Pedro Hasegawa, Tomoko Tanaka, Shin Diogenes, Larissa Amaral, Rogerio Quintiliano Rodrigues, Silvia Helena Andrade, Luis Eduardo Coelho Front Immunol Immunology Anti-fibrillarin autoantibodies are useful for the diagnosis and prognosis of systemic sclerosis (SSc). Anti-fibrillarin produces a clumpy nucleolar pattern in indirect immunofluorescence assay on HEp-2 cells (HEp-2 IFA). Here we develop and validate a reliable cell-based anti-fibrillarin assay (Fibrillarin/CBA) for use in clinical diagnostic laboratories. A TransMembrane Signal was fused to the human fibrillarin gene (TMS-fibrillarin). HEp-2 cells overexpressing transgenic TMS-fibrillarin at the cytoplasmic membrane were used as IFA substrate in the Fibrillarin/CBA. Sixty-two serum samples with nucleolar pattern in the HEp-2 IFA (41 clumpy; 21 homogeneous/punctate) were tested for anti-fibrillarin using Fibrillarin/CBA, immunoprecipitation (IP), line-blot and ELISA. In addition, samples from 106 SSc-patients were evaluated with Fibrillarin/CBA and the results were correlated with disease phenotypes. Thirty-eight of 41 samples with the clumpy nucleolar pattern (92.7%) were positive in the Fibrillarin/CBA, while all 21 samples with other nucleolar patterns were negative. Fibrillarin/CBA results agreed 100% with IP results. Among the 38 Fibrillarin/CBA-positive samples, only 15 (39.5%) and 11 (29%) were positive for anti-fibrillarin in line-blot and ELISA, respectively. Higher frequency of diffuse cutaneous SSc (dcSSc) phenotype (72.7% vs 36.8%; p=0.022), cardiac involvement (36.4% vs 6.5%; p=0.001) and scleroderma renal crisis (18.2% vs 3.3% p = 0.028) was observed in SSc patients with positive compared to negative Fibrillarin/CBA result. Performance of Fibrillarin/CBA in the detection of anti-fibrillarin autoantibodies was comparable to the gold standard IP. Positive Fibrillarin/CBA results correlated with disease phenotypes known to be associated with anti-fibrillarin autoantibodies, underscoring the clinical validation of this novel assay. Frontiers Media S.A. 2022-09-26 /pmc/articles/PMC9549361/ /pubmed/36225928 http://dx.doi.org/10.3389/fimmu.2022.1011110 Text en Copyright © 2022 Keppeke, Satoh, Kayser, Matos, Hasegawa, Tanaka, Diogenes, Amaral, Rodrigues and Andrade https://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
Keppeke, Gerson Dierley
Satoh, Minoru
Kayser, Cristiane
Matos, Pedro
Hasegawa, Tomoko
Tanaka, Shin
Diogenes, Larissa
Amaral, Rogerio Quintiliano
Rodrigues, Silvia Helena
Andrade, Luis Eduardo Coelho
A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
title A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
title_full A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
title_fullStr A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
title_full_unstemmed A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
title_short A cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
title_sort cell-based assay for detection of anti-fibrillarin autoantibodies with performance equivalent to immunoprecipitation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549361/
https://www.ncbi.nlm.nih.gov/pubmed/36225928
http://dx.doi.org/10.3389/fimmu.2022.1011110
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