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Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients

Silicosis patients (SIL) suffer from respiratory disorders and dysregulation of autoimmunity. Frequent complications such as rheumatoid arthritis, systemic sclerosis (SSc) and vasculitis are known in SIL. Furthermore, we reported previously that some SIL exhibited better respiratory conditions in as...

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Autores principales: Lee, Suni, Hayashi, Hiroaki, Kumagai-Takei, Naoko, Matsuzaki, Hidenori, Yoshitome, Kei, Nishimura, Yasumitsu, Uragami, Kozo, Kusaka, Masayasu, Yamamoto, Shoko, Ikeda, Miho, Hatayama, Tamayo, Fujimoto, Wataru, Otsuki, Takemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450599/
https://www.ncbi.nlm.nih.gov/pubmed/28587321
http://dx.doi.org/10.3892/etm.2017.4331
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author Lee, Suni
Hayashi, Hiroaki
Kumagai-Takei, Naoko
Matsuzaki, Hidenori
Yoshitome, Kei
Nishimura, Yasumitsu
Uragami, Kozo
Kusaka, Masayasu
Yamamoto, Shoko
Ikeda, Miho
Hatayama, Tamayo
Fujimoto, Wataru
Otsuki, Takemi
author_facet Lee, Suni
Hayashi, Hiroaki
Kumagai-Takei, Naoko
Matsuzaki, Hidenori
Yoshitome, Kei
Nishimura, Yasumitsu
Uragami, Kozo
Kusaka, Masayasu
Yamamoto, Shoko
Ikeda, Miho
Hatayama, Tamayo
Fujimoto, Wataru
Otsuki, Takemi
author_sort Lee, Suni
collection PubMed
description Silicosis patients (SIL) suffer from respiratory disorders and dysregulation of autoimmunity. Frequent complications such as rheumatoid arthritis, systemic sclerosis (SSc) and vasculitis are known in SIL. Furthermore, we reported previously that some SIL exhibited better respiratory conditions in association with a worse immunological status. In this study, the clinical roles of anti-CENP-B and Scl-70 autoantibodies in SIL were analyzed. The titer index (Log10) of anti-CENP-B autoantibody in SIL was higher than that of healthy volunteers (HV), and that of SSc was higher than those of HV and SIL. This titer index was positively correlated with an assumed immune status of 1 for HV, 2 for SIL, and 3 for SSc. Moreover, although factor analysis revealed that the titer index of the anti-CENP-B autoantibody formed the same factor with the anti-Scl-70 autoantibody, IgG value and age in SIL cases, another extracted factor indicated that the IgA value and anti-Scl-70 antibody were positively related, but anti-CENP-B showed an opposite pattern in the results of the factor analysis. These findings indicated that the titer index of anti-CENP-B autoantibody may be a biomarker for dysregulation in SIL cases. Future clinical follow-up of SIL may therefore require both respiratory and immunological assessment.
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spelling pubmed-54505992017-06-05 Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients Lee, Suni Hayashi, Hiroaki Kumagai-Takei, Naoko Matsuzaki, Hidenori Yoshitome, Kei Nishimura, Yasumitsu Uragami, Kozo Kusaka, Masayasu Yamamoto, Shoko Ikeda, Miho Hatayama, Tamayo Fujimoto, Wataru Otsuki, Takemi Exp Ther Med Articles Silicosis patients (SIL) suffer from respiratory disorders and dysregulation of autoimmunity. Frequent complications such as rheumatoid arthritis, systemic sclerosis (SSc) and vasculitis are known in SIL. Furthermore, we reported previously that some SIL exhibited better respiratory conditions in association with a worse immunological status. In this study, the clinical roles of anti-CENP-B and Scl-70 autoantibodies in SIL were analyzed. The titer index (Log10) of anti-CENP-B autoantibody in SIL was higher than that of healthy volunteers (HV), and that of SSc was higher than those of HV and SIL. This titer index was positively correlated with an assumed immune status of 1 for HV, 2 for SIL, and 3 for SSc. Moreover, although factor analysis revealed that the titer index of the anti-CENP-B autoantibody formed the same factor with the anti-Scl-70 autoantibody, IgG value and age in SIL cases, another extracted factor indicated that the IgA value and anti-Scl-70 antibody were positively related, but anti-CENP-B showed an opposite pattern in the results of the factor analysis. These findings indicated that the titer index of anti-CENP-B autoantibody may be a biomarker for dysregulation in SIL cases. Future clinical follow-up of SIL may therefore require both respiratory and immunological assessment. D.A. Spandidos 2017-06 2017-04-12 /pmc/articles/PMC5450599/ /pubmed/28587321 http://dx.doi.org/10.3892/etm.2017.4331 Text en Copyright: © Lee et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Lee, Suni
Hayashi, Hiroaki
Kumagai-Takei, Naoko
Matsuzaki, Hidenori
Yoshitome, Kei
Nishimura, Yasumitsu
Uragami, Kozo
Kusaka, Masayasu
Yamamoto, Shoko
Ikeda, Miho
Hatayama, Tamayo
Fujimoto, Wataru
Otsuki, Takemi
Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients
title Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients
title_full Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients
title_fullStr Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients
title_full_unstemmed Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients
title_short Clinical evaluation of CENP-B and Scl-70 autoantibodies in silicosis patients
title_sort clinical evaluation of cenp-b and scl-70 autoantibodies in silicosis patients
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450599/
https://www.ncbi.nlm.nih.gov/pubmed/28587321
http://dx.doi.org/10.3892/etm.2017.4331
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