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Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy

Aims: To develop a highly sensitive immunoassay for PLA2R autoantibodies and study the relationship between PLA2R autoantibodies and autoimmune thyroid disease-associated nephropathy. Methods: We applied a highly sensitive time-resolved fluoroimmunoassay to quantitatively detect the concentration of...

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Autores principales: Huang, Biao, Zhang, Yi, Wang, Liang, Wu, Qingqing, Li, Ting, Zhang, Jue, Zhang, Qiuhua, Sheng, Huiming, Bao, Jiandong, Hu, Zhigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204991/
https://www.ncbi.nlm.nih.gov/pubmed/32425952
http://dx.doi.org/10.3389/fimmu.2020.00837
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author Huang, Biao
Zhang, Yi
Wang, Liang
Wu, Qingqing
Li, Ting
Zhang, Jue
Zhang, Qiuhua
Sheng, Huiming
Bao, Jiandong
Hu, Zhigang
author_facet Huang, Biao
Zhang, Yi
Wang, Liang
Wu, Qingqing
Li, Ting
Zhang, Jue
Zhang, Qiuhua
Sheng, Huiming
Bao, Jiandong
Hu, Zhigang
author_sort Huang, Biao
collection PubMed
description Aims: To develop a highly sensitive immunoassay for PLA2R autoantibodies and study the relationship between PLA2R autoantibodies and autoimmune thyroid disease-associated nephropathy. Methods: We applied a highly sensitive time-resolved fluoroimmunoassay to quantitatively detect the concentration of phospholipase A2 receptor (PLA2R) antibodies in the serum of patients with Graves' disease, Hashimoto's thyroiditis (HT), nephrotic patients with idiopathic membranous nephropathy (IMN), and normal controls. We immunohistochemically analyzed the existing PLA2R target antigen in the thyroid tissue of patients with Graves' disease and HT, as well as the nephridial tissue of nephrotic patients with IMN. Results: PLA2R antibody concentrations in the serum of normal controls, patients with nodular goiter, Graves' disease, and HT, as well as patients with IMN were 1.13 ± 0.43, 1.07 ± 0.22, 2.12 ± 2.11, 8.07 ± 4.74, and 15.91 ± 19.50 mg/L, respectively. PLA2R antibody concentration in the serum and the area under the receiver operating characteristic curve in patients with HT and IMN were increased significantly. Immunohistochemistry revealed obvious staining of PLA2R in tissues from patients with HT, with a positive rate of 66.67%. Conclusions: PLA2R is a potential pathogenic target antigen for HT, and the production of PLA2R antibodies may cause autoimmune thyroid disease-associated nephropathy.
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spelling pubmed-72049912020-05-18 Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy Huang, Biao Zhang, Yi Wang, Liang Wu, Qingqing Li, Ting Zhang, Jue Zhang, Qiuhua Sheng, Huiming Bao, Jiandong Hu, Zhigang Front Immunol Immunology Aims: To develop a highly sensitive immunoassay for PLA2R autoantibodies and study the relationship between PLA2R autoantibodies and autoimmune thyroid disease-associated nephropathy. Methods: We applied a highly sensitive time-resolved fluoroimmunoassay to quantitatively detect the concentration of phospholipase A2 receptor (PLA2R) antibodies in the serum of patients with Graves' disease, Hashimoto's thyroiditis (HT), nephrotic patients with idiopathic membranous nephropathy (IMN), and normal controls. We immunohistochemically analyzed the existing PLA2R target antigen in the thyroid tissue of patients with Graves' disease and HT, as well as the nephridial tissue of nephrotic patients with IMN. Results: PLA2R antibody concentrations in the serum of normal controls, patients with nodular goiter, Graves' disease, and HT, as well as patients with IMN were 1.13 ± 0.43, 1.07 ± 0.22, 2.12 ± 2.11, 8.07 ± 4.74, and 15.91 ± 19.50 mg/L, respectively. PLA2R antibody concentration in the serum and the area under the receiver operating characteristic curve in patients with HT and IMN were increased significantly. Immunohistochemistry revealed obvious staining of PLA2R in tissues from patients with HT, with a positive rate of 66.67%. Conclusions: PLA2R is a potential pathogenic target antigen for HT, and the production of PLA2R antibodies may cause autoimmune thyroid disease-associated nephropathy. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7204991/ /pubmed/32425952 http://dx.doi.org/10.3389/fimmu.2020.00837 Text en Copyright © 2020 Huang, Zhang, Wang, Wu, Li, Zhang, Zhang, Sheng, Bao and Hu. http://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
Huang, Biao
Zhang, Yi
Wang, Liang
Wu, Qingqing
Li, Ting
Zhang, Jue
Zhang, Qiuhua
Sheng, Huiming
Bao, Jiandong
Hu, Zhigang
Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy
title Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy
title_full Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy
title_fullStr Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy
title_full_unstemmed Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy
title_short Phospholipase A2 Receptor Autoantibodies as a Novel Serological Biomarker for Autoimmune Thyroid Disease Associated Nephropathy
title_sort phospholipase a2 receptor autoantibodies as a novel serological biomarker for autoimmune thyroid disease associated nephropathy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204991/
https://www.ncbi.nlm.nih.gov/pubmed/32425952
http://dx.doi.org/10.3389/fimmu.2020.00837
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