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SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?

Immunoglobulin A nephropathy, the most common primary glomerulonephritis worldwide, is a leading cause of chronic kidney disease and end-stage kidney failure. Several cases of immunoglobulin A nephropathy relapse in native kidneys have been described after COVID-19 vaccination or SARS-CoV-2 infectio...

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Autores principales: Jankowski, Eric, Schlosser, Mandy, Wiech, Thorsten, Wolf, Gunter, Busch, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393859/
https://www.ncbi.nlm.nih.gov/pubmed/37341968
http://dx.doi.org/10.1007/s40620-023-01684-y
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author Jankowski, Eric
Schlosser, Mandy
Wiech, Thorsten
Wolf, Gunter
Busch, Martin
author_facet Jankowski, Eric
Schlosser, Mandy
Wiech, Thorsten
Wolf, Gunter
Busch, Martin
author_sort Jankowski, Eric
collection PubMed
description Immunoglobulin A nephropathy, the most common primary glomerulonephritis worldwide, is a leading cause of chronic kidney disease and end-stage kidney failure. Several cases of immunoglobulin A nephropathy relapse in native kidneys have been described after COVID-19 vaccination or SARS-CoV-2 infection. Here, we report the case of a 52-year-old kidney transplant recipient who had a stable transplant function for more than 14 years, with a glomerular filtration rate above 30 ml/min/1.73 m(2). The patient had been vaccinated against COVID-19 four times with the Pfizer-BioNTech vaccine, most recently in March 2022. Eight weeks after a symptomatic SARS-CoV-2 infection in June 2022, his glomerular filtration rate had decreased by more than 50%, and his proteinuria increased to 17.5 g per day. A renal biopsy indicated highly active immunoglobulin A nephritis. Despite steroid therapy, the function of the transplanted kidney deteriorated, and long-term dialysis became necessary because of recurrence of his underlying renal disease. This case report provides what is, to our knowledge, the first description of recurrent immunoglobulin A nephropathy in a kidney transplant recipient after SARS-CoV-2 infection leading to severe transplant failure and finally graft loss. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40620-023-01684-y.
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spelling pubmed-103938592023-08-03 SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation? Jankowski, Eric Schlosser, Mandy Wiech, Thorsten Wolf, Gunter Busch, Martin J Nephrol Case Report Immunoglobulin A nephropathy, the most common primary glomerulonephritis worldwide, is a leading cause of chronic kidney disease and end-stage kidney failure. Several cases of immunoglobulin A nephropathy relapse in native kidneys have been described after COVID-19 vaccination or SARS-CoV-2 infection. Here, we report the case of a 52-year-old kidney transplant recipient who had a stable transplant function for more than 14 years, with a glomerular filtration rate above 30 ml/min/1.73 m(2). The patient had been vaccinated against COVID-19 four times with the Pfizer-BioNTech vaccine, most recently in March 2022. Eight weeks after a symptomatic SARS-CoV-2 infection in June 2022, his glomerular filtration rate had decreased by more than 50%, and his proteinuria increased to 17.5 g per day. A renal biopsy indicated highly active immunoglobulin A nephritis. Despite steroid therapy, the function of the transplanted kidney deteriorated, and long-term dialysis became necessary because of recurrence of his underlying renal disease. This case report provides what is, to our knowledge, the first description of recurrent immunoglobulin A nephropathy in a kidney transplant recipient after SARS-CoV-2 infection leading to severe transplant failure and finally graft loss. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40620-023-01684-y. Springer International Publishing 2023-06-21 2023 /pmc/articles/PMC10393859/ /pubmed/37341968 http://dx.doi.org/10.1007/s40620-023-01684-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Case Report
Jankowski, Eric
Schlosser, Mandy
Wiech, Thorsten
Wolf, Gunter
Busch, Martin
SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
title SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
title_full SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
title_fullStr SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
title_full_unstemmed SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
title_short SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
title_sort sars-cov-2 infection: a possible trigger for the recurrence of iga nephropathy after kidney transplantation?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10393859/
https://www.ncbi.nlm.nih.gov/pubmed/37341968
http://dx.doi.org/10.1007/s40620-023-01684-y
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