Membranous Nephropathy (MN) Recurrence After Renal Transplantation

Primary membranous nephropathy (MN) is a frequent cause of NS in adults. In native kidneys the disease may progress to ESRD in the long term, in some 40–50% of untreated patients. The identification of the pathogenic role of anti-podocyte autoantibodies and the development of new therapeutic options...

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Main Authors: Patrizia Passerini, Silvia Malvica, Federica Tripodi, Roberta Cerutti, Piergiorgio Messa
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.01326/full
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spelling doaj-de462adb40fe4db4882c61eb9aa09b682020-11-25T01:08:08ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-06-011010.3389/fimmu.2019.01326459625Membranous Nephropathy (MN) Recurrence After Renal TransplantationPatrizia Passerini0Silvia Malvica1Federica Tripodi2Roberta Cerutti3Piergiorgio Messa4Piergiorgio Messa5Dialysis, and Renal Transplant Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, ItalyDialysis, and Renal Transplant Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, ItalyDialysis, and Renal Transplant Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, ItalyDialysis, and Renal Transplant Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, ItalyDialysis, and Renal Transplant Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, ItalyDepartment of Clinical Science and Community, Università degli Studi di Milano, Milan, ItalyPrimary membranous nephropathy (MN) is a frequent cause of NS in adults. In native kidneys the disease may progress to ESRD in the long term, in some 40–50% of untreated patients. The identification of the pathogenic role of anti-podocyte autoantibodies and the development of new therapeutic options has achieved an amelioration in the prognosis of this disease. MN may also develop in renal allograft as a recurrent or a de novo disease. Since the de novo MN may have some different pathogenetic and morphologic features compared to recurrent MN, in the present paper we will deal only with the recurrent disease. The true incidence of the recurrent form is difficult to assess. This is mainly due to the variable graft biopsy policies in kidney transplantation, among the different transplant centers. Anti-phospholipase A2 receptor (PLA2R) autoantibodies are detected in 70–80% of patients. The knowledge of anti-PLA2R status before transplant is useful in predicting the risk of recurrence. In addition, the serial survey of the anti-PLA2R titers is important to assess the rate of disease progression and the response to treatment. Currently, there are no established guidelines for prevention and treatment of recurrent MN. Symptomatic therapy may help to reduce the signs and symptoms related to the nephrotic syndrome. Anecdotal cases of response to cyclical therapy with steroids and cyclophosphamide have been published. Promising results have been reported with rituximab in both prophylaxis and treatment of recurrence. However, these results are based on observational data, and prospective controlled trials are still missing.https://www.frontiersin.org/article/10.3389/fimmu.2019.01326/fullmembranous nephropathyrecurrent membranous nephropathykidney transplantproteinuriaanti-PLA2R antibodiesrituximab
collection DOAJ
language English
format Article
sources DOAJ
author Patrizia Passerini
Silvia Malvica
Federica Tripodi
Roberta Cerutti
Piergiorgio Messa
Piergiorgio Messa
spellingShingle Patrizia Passerini
Silvia Malvica
Federica Tripodi
Roberta Cerutti
Piergiorgio Messa
Piergiorgio Messa
Membranous Nephropathy (MN) Recurrence After Renal Transplantation
Frontiers in Immunology
membranous nephropathy
recurrent membranous nephropathy
kidney transplant
proteinuria
anti-PLA2R antibodies
rituximab
author_facet Patrizia Passerini
Silvia Malvica
Federica Tripodi
Roberta Cerutti
Piergiorgio Messa
Piergiorgio Messa
author_sort Patrizia Passerini
title Membranous Nephropathy (MN) Recurrence After Renal Transplantation
title_short Membranous Nephropathy (MN) Recurrence After Renal Transplantation
title_full Membranous Nephropathy (MN) Recurrence After Renal Transplantation
title_fullStr Membranous Nephropathy (MN) Recurrence After Renal Transplantation
title_full_unstemmed Membranous Nephropathy (MN) Recurrence After Renal Transplantation
title_sort membranous nephropathy (mn) recurrence after renal transplantation
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-06-01
description Primary membranous nephropathy (MN) is a frequent cause of NS in adults. In native kidneys the disease may progress to ESRD in the long term, in some 40–50% of untreated patients. The identification of the pathogenic role of anti-podocyte autoantibodies and the development of new therapeutic options has achieved an amelioration in the prognosis of this disease. MN may also develop in renal allograft as a recurrent or a de novo disease. Since the de novo MN may have some different pathogenetic and morphologic features compared to recurrent MN, in the present paper we will deal only with the recurrent disease. The true incidence of the recurrent form is difficult to assess. This is mainly due to the variable graft biopsy policies in kidney transplantation, among the different transplant centers. Anti-phospholipase A2 receptor (PLA2R) autoantibodies are detected in 70–80% of patients. The knowledge of anti-PLA2R status before transplant is useful in predicting the risk of recurrence. In addition, the serial survey of the anti-PLA2R titers is important to assess the rate of disease progression and the response to treatment. Currently, there are no established guidelines for prevention and treatment of recurrent MN. Symptomatic therapy may help to reduce the signs and symptoms related to the nephrotic syndrome. Anecdotal cases of response to cyclical therapy with steroids and cyclophosphamide have been published. Promising results have been reported with rituximab in both prophylaxis and treatment of recurrence. However, these results are based on observational data, and prospective controlled trials are still missing.
topic membranous nephropathy
recurrent membranous nephropathy
kidney transplant
proteinuria
anti-PLA2R antibodies
rituximab
url https://www.frontiersin.org/article/10.3389/fimmu.2019.01326/full
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