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The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome

OBJECTIVE: The aim of this study was to characterize the subsets of circulating CD56(+) NK cells in pSS patients and their potential value in the diagnosis and/or prediction of prognosis in patients with pSS. METHODS: We included 52 pSS patients fulfilling the 2002 AECG criteria or 2012 ACR criteria...

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Autores principales: Ming, Bingxia, Wu, Tong, Cai, Shaozhe, Hu, Peng, Tang, Jungen, Zheng, Fang, Ye, Cong, Dong, Lingli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368214/
https://www.ncbi.nlm.nih.gov/pubmed/32695834
http://dx.doi.org/10.1155/2020/7523914
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author Ming, Bingxia
Wu, Tong
Cai, Shaozhe
Hu, Peng
Tang, Jungen
Zheng, Fang
Ye, Cong
Dong, Lingli
author_facet Ming, Bingxia
Wu, Tong
Cai, Shaozhe
Hu, Peng
Tang, Jungen
Zheng, Fang
Ye, Cong
Dong, Lingli
author_sort Ming, Bingxia
collection PubMed
description OBJECTIVE: The aim of this study was to characterize the subsets of circulating CD56(+) NK cells in pSS patients and their potential value in the diagnosis and/or prediction of prognosis in patients with pSS. METHODS: We included 52 pSS patients fulfilling the 2002 AECG criteria or 2012 ACR criteria and 20 age- and gender-matched healthy volunteers. The frequency and absolute number of NK cells and CD56 NK cell subsets in peripheral blood samples were detected by flow cytometry. Other laboratory parameters such as the IgG level and complement protein levels were extracted from the clinical system. RESULTS: Both the frequency and the absolute number of peripheral blood NK cells were reduced in pSS patients compared to healthy controls. The proportion of CD56(bright) NK cell subset was increased, and the proportion of CD56(dim) NK cell subset was decreased among NK cells, resulting in the ratio of CD56(bright) NK to CD56(dim) NK which was significantly elevated in pSS patients. ROC analysis indicated that the AUC of CD56(bright) NK/CD56(dim) NK ratio was 0.838, and the best diagnostic cut-off point was 0.0487 for pSS patients. Furthermore, this CD56(bright) NK/CD56(dim) NK ratio was positively correlated with the IgG level and negatively correlated with the complement protein C3 and C4 levels. More importantly, the CD56(bright)/CD56(dim) NK ratio was either slightly increased or not changed in other autoimmune diseases such as SLE and IgG4-related disease. CONCLUSION: Our findings suggest that the ratio of blood CD56(bright) NK to CD56(dim) NK might have a diagnostic value relatively specific for pSS.
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spelling pubmed-73682142020-07-20 The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome Ming, Bingxia Wu, Tong Cai, Shaozhe Hu, Peng Tang, Jungen Zheng, Fang Ye, Cong Dong, Lingli J Immunol Res Research Article OBJECTIVE: The aim of this study was to characterize the subsets of circulating CD56(+) NK cells in pSS patients and their potential value in the diagnosis and/or prediction of prognosis in patients with pSS. METHODS: We included 52 pSS patients fulfilling the 2002 AECG criteria or 2012 ACR criteria and 20 age- and gender-matched healthy volunteers. The frequency and absolute number of NK cells and CD56 NK cell subsets in peripheral blood samples were detected by flow cytometry. Other laboratory parameters such as the IgG level and complement protein levels were extracted from the clinical system. RESULTS: Both the frequency and the absolute number of peripheral blood NK cells were reduced in pSS patients compared to healthy controls. The proportion of CD56(bright) NK cell subset was increased, and the proportion of CD56(dim) NK cell subset was decreased among NK cells, resulting in the ratio of CD56(bright) NK to CD56(dim) NK which was significantly elevated in pSS patients. ROC analysis indicated that the AUC of CD56(bright) NK/CD56(dim) NK ratio was 0.838, and the best diagnostic cut-off point was 0.0487 for pSS patients. Furthermore, this CD56(bright) NK/CD56(dim) NK ratio was positively correlated with the IgG level and negatively correlated with the complement protein C3 and C4 levels. More importantly, the CD56(bright)/CD56(dim) NK ratio was either slightly increased or not changed in other autoimmune diseases such as SLE and IgG4-related disease. CONCLUSION: Our findings suggest that the ratio of blood CD56(bright) NK to CD56(dim) NK might have a diagnostic value relatively specific for pSS. Hindawi 2020-07-09 /pmc/articles/PMC7368214/ /pubmed/32695834 http://dx.doi.org/10.1155/2020/7523914 Text en Copyright © 2020 Bingxia Ming et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ming, Bingxia
Wu, Tong
Cai, Shaozhe
Hu, Peng
Tang, Jungen
Zheng, Fang
Ye, Cong
Dong, Lingli
The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome
title The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome
title_full The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome
title_fullStr The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome
title_full_unstemmed The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome
title_short The Increased Ratio of Blood CD56(bright) NK to CD56(dim) NK Is a Distinguishing Feature of Primary Sjögren's Syndrome
title_sort increased ratio of blood cd56(bright) nk to cd56(dim) nk is a distinguishing feature of primary sjögren's syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368214/
https://www.ncbi.nlm.nih.gov/pubmed/32695834
http://dx.doi.org/10.1155/2020/7523914
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