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HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy

Idiopathic membranous nephropathy (IMN) is known to be associated with antibodies acting on the M-type phospholipase A2 receptor (PLA2R) of the podocyte. However, the mechanism underlying de novo membranous nephropathy (dn MN) posttransplantation remains unclear. In this study, we aimed to elucidate...

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Autores principales: Wen, Jiqiu, Xie, Kenan, Zhang, Mingchao, Chen, Jinsong, Zhang, Jiong, Cheng, Dongrui, Li, Xue, Ji, Shuming, Liu, Zhihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402576/
https://www.ncbi.nlm.nih.gov/pubmed/27631233
http://dx.doi.org/10.1097/MD.0000000000004809
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author Wen, Jiqiu
Xie, Kenan
Zhang, Mingchao
Chen, Jinsong
Zhang, Jiong
Cheng, Dongrui
Li, Xue
Ji, Shuming
Liu, Zhihong
author_facet Wen, Jiqiu
Xie, Kenan
Zhang, Mingchao
Chen, Jinsong
Zhang, Jiong
Cheng, Dongrui
Li, Xue
Ji, Shuming
Liu, Zhihong
author_sort Wen, Jiqiu
collection PubMed
description Idiopathic membranous nephropathy (IMN) is known to be associated with antibodies acting on the M-type phospholipase A2 receptor (PLA2R) of the podocyte. However, the mechanism underlying de novo membranous nephropathy (dn MN) posttransplantation remains unclear. In this study, we aimed to elucidate the mechanism underlying dn MN. We selected 8 cases with dn MN and compared them to 20 IMN cases. Fifteen cases of stable grafts were selected as controls. Several differences between the dn MN group and the IMN group were detected. IgG4 showed negligible positive staining in patients with dn MN, while it was predominant in the IMN group (1/8 vs 20/20, P < 0.001). Serum anti-PLA2R antibodies and anti-PLA2R antibodies of the podocyte were very few in the dn MN patients; however, these antibodies were detected in most of the IMN patients (serum anti-PLA2R antibodies: 1/8 vs 16/20, P = 0.002, anti-PLA2R antibodies of the podocyte: 0/8 vs 17/20, P < 0.001). The dn MN patients also showed higher ratio of interstitial inflammation, peritubular capillaritis, and peritubular capillary C4d deposition. Importantly, human leukocyte antigens (HLA)-DR expression was detected on the podocytes in most of the dn MN patients, but none of the IMN patients and stable graft patients showed HLA-DR expression. These data suggested that the PLA2R pathway, which is known to play a role in IMN, was not involved in the mechanism underlying dn MN. On the contrary, dn MN might be associated with the alloimmune response directed against the podocyte.
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spelling pubmed-54025762017-04-27 HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy Wen, Jiqiu Xie, Kenan Zhang, Mingchao Chen, Jinsong Zhang, Jiong Cheng, Dongrui Li, Xue Ji, Shuming Liu, Zhihong Medicine (Baltimore) 5200 Idiopathic membranous nephropathy (IMN) is known to be associated with antibodies acting on the M-type phospholipase A2 receptor (PLA2R) of the podocyte. However, the mechanism underlying de novo membranous nephropathy (dn MN) posttransplantation remains unclear. In this study, we aimed to elucidate the mechanism underlying dn MN. We selected 8 cases with dn MN and compared them to 20 IMN cases. Fifteen cases of stable grafts were selected as controls. Several differences between the dn MN group and the IMN group were detected. IgG4 showed negligible positive staining in patients with dn MN, while it was predominant in the IMN group (1/8 vs 20/20, P < 0.001). Serum anti-PLA2R antibodies and anti-PLA2R antibodies of the podocyte were very few in the dn MN patients; however, these antibodies were detected in most of the IMN patients (serum anti-PLA2R antibodies: 1/8 vs 16/20, P = 0.002, anti-PLA2R antibodies of the podocyte: 0/8 vs 17/20, P < 0.001). The dn MN patients also showed higher ratio of interstitial inflammation, peritubular capillaritis, and peritubular capillary C4d deposition. Importantly, human leukocyte antigens (HLA)-DR expression was detected on the podocytes in most of the dn MN patients, but none of the IMN patients and stable graft patients showed HLA-DR expression. These data suggested that the PLA2R pathway, which is known to play a role in IMN, was not involved in the mechanism underlying dn MN. On the contrary, dn MN might be associated with the alloimmune response directed against the podocyte. Wolters Kluwer Health 2016-09-16 /pmc/articles/PMC5402576/ /pubmed/27631233 http://dx.doi.org/10.1097/MD.0000000000004809 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0
spellingShingle 5200
Wen, Jiqiu
Xie, Kenan
Zhang, Mingchao
Chen, Jinsong
Zhang, Jiong
Cheng, Dongrui
Li, Xue
Ji, Shuming
Liu, Zhihong
HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
title HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
title_full HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
title_fullStr HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
title_full_unstemmed HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
title_short HLA-DR, and not PLA2R, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
title_sort hla-dr, and not pla2r, is expressed on the podocytes in kidney allografts in de novo membranous nephropathy
topic 5200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402576/
https://www.ncbi.nlm.nih.gov/pubmed/27631233
http://dx.doi.org/10.1097/MD.0000000000004809
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