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Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus

Background. Serum concentrations of soluble interleukin-7 receptor (sIL-7R) and anti-C1q antibody have recently been identified as unique serological markers for lupus nephritis (LN) in patients with systemic lupus erythematosus (SLE). In this study, we evaluated the correlation of serum sIL-7R and...

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Autores principales: Chi, Shuhong, Xue, Jing, Li, Feng, Zhu, Caixia, Yu, Yunxia, Li, Haibo, Wang, Xuemei, Zhang, Yurong, Yang, Jijuan, Zhou, Shaolan, Yang, Lijuan, Ji, Chen, Liu, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812203/
https://www.ncbi.nlm.nih.gov/pubmed/27069677
http://dx.doi.org/10.1155/2016/8252605
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author Chi, Shuhong
Xue, Jing
Li, Feng
Zhu, Caixia
Yu, Yunxia
Li, Haibo
Wang, Xuemei
Zhang, Yurong
Yang, Jijuan
Zhou, Shaolan
Yang, Lijuan
Ji, Chen
Liu, Xiaoming
author_facet Chi, Shuhong
Xue, Jing
Li, Feng
Zhu, Caixia
Yu, Yunxia
Li, Haibo
Wang, Xuemei
Zhang, Yurong
Yang, Jijuan
Zhou, Shaolan
Yang, Lijuan
Ji, Chen
Liu, Xiaoming
author_sort Chi, Shuhong
collection PubMed
description Background. Serum concentrations of soluble interleukin-7 receptor (sIL-7R) and anti-C1q antibody have recently been identified as unique serological markers for lupus nephritis (LN) in patients with systemic lupus erythematosus (SLE). In this study, we evaluated the correlation of serum sIL-7R and anti-C1q in SLE patients. Methods. Sera from 134 patients with SLE and 84 healthy cohorts were tested for levels of sIL-7R and anti-C1q antibodies in terms of ELISA. Correlations of the sIL-7R and anti-C1q autoantibodies were evaluated. Results. The serum concentrations of sIL-7R and anti-C1q antibodies were significantly higher in SLE patients and LN patients in comparison with healthy individuals/controls and SLE patients with non-LN, respectively. In addition, both sIL-7R and anti-C1q concentrations were found to significantly correlate with the SLE disease activity as evaluated by SLEDAI scores. Interestingly, the serum sIL-7R concentration was strongly correlated with the level of anti-C1q antibodies (r = 0.2871, p = 0.0008) but not statistically correlated with other serological markers, including the anti-dsDNA and complements C3 and C4 concentrations in SLE patients. Conclusion. Both serum sIL-7R and anti-C1q antibodies were strongly associated with disease activity and LN in SLE patients, suggesting that they may be reliable serological markers for identification of SLE patients with active diseases and LN.
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spelling pubmed-48122032016-04-11 Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus Chi, Shuhong Xue, Jing Li, Feng Zhu, Caixia Yu, Yunxia Li, Haibo Wang, Xuemei Zhang, Yurong Yang, Jijuan Zhou, Shaolan Yang, Lijuan Ji, Chen Liu, Xiaoming Autoimmune Dis Research Article Background. Serum concentrations of soluble interleukin-7 receptor (sIL-7R) and anti-C1q antibody have recently been identified as unique serological markers for lupus nephritis (LN) in patients with systemic lupus erythematosus (SLE). In this study, we evaluated the correlation of serum sIL-7R and anti-C1q in SLE patients. Methods. Sera from 134 patients with SLE and 84 healthy cohorts were tested for levels of sIL-7R and anti-C1q antibodies in terms of ELISA. Correlations of the sIL-7R and anti-C1q autoantibodies were evaluated. Results. The serum concentrations of sIL-7R and anti-C1q antibodies were significantly higher in SLE patients and LN patients in comparison with healthy individuals/controls and SLE patients with non-LN, respectively. In addition, both sIL-7R and anti-C1q concentrations were found to significantly correlate with the SLE disease activity as evaluated by SLEDAI scores. Interestingly, the serum sIL-7R concentration was strongly correlated with the level of anti-C1q antibodies (r = 0.2871, p = 0.0008) but not statistically correlated with other serological markers, including the anti-dsDNA and complements C3 and C4 concentrations in SLE patients. Conclusion. Both serum sIL-7R and anti-C1q antibodies were strongly associated with disease activity and LN in SLE patients, suggesting that they may be reliable serological markers for identification of SLE patients with active diseases and LN. Hindawi Publishing Corporation 2016 2016-03-16 /pmc/articles/PMC4812203/ /pubmed/27069677 http://dx.doi.org/10.1155/2016/8252605 Text en Copyright © 2016 Shuhong Chi et al. https://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
Chi, Shuhong
Xue, Jing
Li, Feng
Zhu, Caixia
Yu, Yunxia
Li, Haibo
Wang, Xuemei
Zhang, Yurong
Yang, Jijuan
Zhou, Shaolan
Yang, Lijuan
Ji, Chen
Liu, Xiaoming
Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus
title Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus
title_full Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus
title_fullStr Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus
title_full_unstemmed Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus
title_short Correlation of Serum Soluble Interleukin-7 Receptor and Anti-C1q Antibody in Patients with Systemic Lupus Erythematosus
title_sort correlation of serum soluble interleukin-7 receptor and anti-c1q antibody in patients with systemic lupus erythematosus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812203/
https://www.ncbi.nlm.nih.gov/pubmed/27069677
http://dx.doi.org/10.1155/2016/8252605
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