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A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing
OBJECTIVES: Anti-TIF1γ is an important autoantibody in the diagnosis of cancer-associated dermatomyositis and the most common autoantibody in juvenile onset dermatomyositis. Its reliable detection is important to instigate further investigations into underlying malignancy in adults. We previously sh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831764/ https://www.ncbi.nlm.nih.gov/pubmed/35154119 http://dx.doi.org/10.3389/fimmu.2022.804037 |
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author | Mulhearn, Ben Li, Danyang McMorrow, Fionnuala Lu, Hui McHugh, Neil J. Tansley, Sarah L. |
author_facet | Mulhearn, Ben Li, Danyang McMorrow, Fionnuala Lu, Hui McHugh, Neil J. Tansley, Sarah L. |
author_sort | Mulhearn, Ben |
collection | PubMed |
description | OBJECTIVES: Anti-TIF1γ is an important autoantibody in the diagnosis of cancer-associated dermatomyositis and the most common autoantibody in juvenile onset dermatomyositis. Its reliable detection is important to instigate further investigations into underlying malignancy in adults. We previously showed that commercial assays using line and dot blots do not reliably detect anti-TIF1γ. We aimed to test a new commercial ELISA and compare with previously obtained protein immunoprecipitation. METHODS: Radio-labelled immunoprecipitation had previously been used to determine the autoantibody status of patients with immune-mediated inflammatory myopathies and several healthy controls. ELISA was undertaken on healthy control and anti-TIF1γ sera and compared to previous immunoprecipitation data. RESULTS: A total of 110 serum samples were analysed: 42 myositis patients with anti- TIF1γ and 68 autoantibody negative healthy control sera. Anti-TIF1γ was detected by ELISA in 41 out of 42 of the anti-TIF1γ-positive samples by immunoprecipitation, and in none of the healthy controls, giving a sensitivity of 97.6% and specificity of 100%. The false negative rate was 2%. CONCLUSION: ELISA is an affordable and time-efficient method which is accurate in detecting anti-TIF1γ. |
format | Online Article Text |
id | pubmed-8831764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88317642022-02-12 A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing Mulhearn, Ben Li, Danyang McMorrow, Fionnuala Lu, Hui McHugh, Neil J. Tansley, Sarah L. Front Immunol Immunology OBJECTIVES: Anti-TIF1γ is an important autoantibody in the diagnosis of cancer-associated dermatomyositis and the most common autoantibody in juvenile onset dermatomyositis. Its reliable detection is important to instigate further investigations into underlying malignancy in adults. We previously showed that commercial assays using line and dot blots do not reliably detect anti-TIF1γ. We aimed to test a new commercial ELISA and compare with previously obtained protein immunoprecipitation. METHODS: Radio-labelled immunoprecipitation had previously been used to determine the autoantibody status of patients with immune-mediated inflammatory myopathies and several healthy controls. ELISA was undertaken on healthy control and anti-TIF1γ sera and compared to previous immunoprecipitation data. RESULTS: A total of 110 serum samples were analysed: 42 myositis patients with anti- TIF1γ and 68 autoantibody negative healthy control sera. Anti-TIF1γ was detected by ELISA in 41 out of 42 of the anti-TIF1γ-positive samples by immunoprecipitation, and in none of the healthy controls, giving a sensitivity of 97.6% and specificity of 100%. The false negative rate was 2%. CONCLUSION: ELISA is an affordable and time-efficient method which is accurate in detecting anti-TIF1γ. Frontiers Media S.A. 2022-01-28 /pmc/articles/PMC8831764/ /pubmed/35154119 http://dx.doi.org/10.3389/fimmu.2022.804037 Text en Copyright © 2022 Mulhearn, Li, McMorrow, Lu, McHugh and Tansley 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 Mulhearn, Ben Li, Danyang McMorrow, Fionnuala Lu, Hui McHugh, Neil J. Tansley, Sarah L. A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing |
title | A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing |
title_full | A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing |
title_fullStr | A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing |
title_full_unstemmed | A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing |
title_short | A Commercial Anti-TIF1γ ELISA Is Superior to Line and Dot Blot and Should Be Considered as Part of Routine Myositis-Specific Antibody Testing |
title_sort | commercial anti-tif1γ elisa is superior to line and dot blot and should be considered as part of routine myositis-specific antibody testing |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831764/ https://www.ncbi.nlm.nih.gov/pubmed/35154119 http://dx.doi.org/10.3389/fimmu.2022.804037 |
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