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What autoantibody tests should become widely available to help scleroderma diagnosis and management?
Anti-Th/To autoantibodies have been recognized as serological markers of systemic sclerosis (SSc) for more than 20 years. However, validated immunoassay kits to test this specificity have not been commercially available. SSc autoantibodies are basically mutually exclusive and are associated with a c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978467/ https://www.ncbi.nlm.nih.gov/pubmed/23856077 http://dx.doi.org/10.1186/ar4241 |
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author | Muro, Yoshinao Sugiura, Kazumitsu Akiyama, Masashi |
author_facet | Muro, Yoshinao Sugiura, Kazumitsu Akiyama, Masashi |
author_sort | Muro, Yoshinao |
collection | PubMed |
description | Anti-Th/To autoantibodies have been recognized as serological markers of systemic sclerosis (SSc) for more than 20 years. However, validated immunoassay kits to test this specificity have not been commercially available. SSc autoantibodies are basically mutually exclusive and are associated with a certain subset of the disease and/or with organ involvement. Anti-Th/To are generally considered to be markers of the limited cutaneous type of SSc with the involvement of certain internal organs. The excellent correlation between anti-Rpp25 as detected by their novel chemiluminescent method and anti-Th/To as detected by immunoprecipitation suggest that the new assays may become widely available tests for clinicians in future and could help to clarify the clinical significance of anti-Th/To in SSc as well as other conditions over different races or countries. |
format | Online Article Text |
id | pubmed-3978467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39784672014-04-09 What autoantibody tests should become widely available to help scleroderma diagnosis and management? Muro, Yoshinao Sugiura, Kazumitsu Akiyama, Masashi Arthritis Res Ther Editorial Anti-Th/To autoantibodies have been recognized as serological markers of systemic sclerosis (SSc) for more than 20 years. However, validated immunoassay kits to test this specificity have not been commercially available. SSc autoantibodies are basically mutually exclusive and are associated with a certain subset of the disease and/or with organ involvement. Anti-Th/To are generally considered to be markers of the limited cutaneous type of SSc with the involvement of certain internal organs. The excellent correlation between anti-Rpp25 as detected by their novel chemiluminescent method and anti-Th/To as detected by immunoprecipitation suggest that the new assays may become widely available tests for clinicians in future and could help to clarify the clinical significance of anti-Th/To in SSc as well as other conditions over different races or countries. BioMed Central 2013 2013-07-08 /pmc/articles/PMC3978467/ /pubmed/23856077 http://dx.doi.org/10.1186/ar4241 Text en Copyright © 2013 BioMed Central Ltd |
spellingShingle | Editorial Muro, Yoshinao Sugiura, Kazumitsu Akiyama, Masashi What autoantibody tests should become widely available to help scleroderma diagnosis and management? |
title | What autoantibody tests should become widely available to help scleroderma diagnosis and management? |
title_full | What autoantibody tests should become widely available to help scleroderma diagnosis and management? |
title_fullStr | What autoantibody tests should become widely available to help scleroderma diagnosis and management? |
title_full_unstemmed | What autoantibody tests should become widely available to help scleroderma diagnosis and management? |
title_short | What autoantibody tests should become widely available to help scleroderma diagnosis and management? |
title_sort | what autoantibody tests should become widely available to help scleroderma diagnosis and management? |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978467/ https://www.ncbi.nlm.nih.gov/pubmed/23856077 http://dx.doi.org/10.1186/ar4241 |
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