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COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report

INTRODUCTION: Immunosuppressive therapy is associated with an increased risk of severe courses of SARS-CoV-2 infection, with frequently delayed viral clearance. We report a case of an acute kidney transplant failure in persistent SARS-CoV-2 infection in a patient with absolute B-cell depletion after...

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Autores principales: Boss, Kristina, Konik, Margarethe, Bräsen, Jan Hinrich, Schmitz, Jessica, Jürgens, Christiane, Kribben, Andreas, Witzke, Oliver, Dolff, Sebastian, Gäckler, Anja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873206/
https://www.ncbi.nlm.nih.gov/pubmed/36694123
http://dx.doi.org/10.1186/s12882-023-03070-z
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author Boss, Kristina
Konik, Margarethe
Bräsen, Jan Hinrich
Schmitz, Jessica
Jürgens, Christiane
Kribben, Andreas
Witzke, Oliver
Dolff, Sebastian
Gäckler, Anja
author_facet Boss, Kristina
Konik, Margarethe
Bräsen, Jan Hinrich
Schmitz, Jessica
Jürgens, Christiane
Kribben, Andreas
Witzke, Oliver
Dolff, Sebastian
Gäckler, Anja
author_sort Boss, Kristina
collection PubMed
description INTRODUCTION: Immunosuppressive therapy is associated with an increased risk of severe courses of SARS-CoV-2 infection, with frequently delayed viral clearance. We report a case of an acute kidney transplant failure in persistent SARS-CoV-2 infection in a patient with absolute B-cell depletion after administration of rituximab for AB0-incompatible living donor kidney transplantation. CASE PRESENTATION: A 34-year-old unvaccinated patient is diagnosed with SARS-CoV-2 infection four months after kidney transplantation. With only mild symptoms and an estimated glomerular filtration rate (eGFR) of 44 ml/min/1.73 m(2), therapy with molnupiravir was initially given. Within the next eight weeks, transplant biopsies were performed for acute graft failure. These showed acute T-cell rejection with severe acute tubular epithelial damage with only mild interstitial fibrosis and tubular atrophy (BANFF cat. 4 IB), and borderline rejection (BANFF cat. 3). A therapy with prednisolone and intravenous immunoglobulins was performed twice. With unchanged graft failure, the third biopsy also formally showed BANFF cat. 4 IB. However, fluorescence in situ hybridization detected SARS-CoV-2 viruses in large portions of the distal tubules. After nine weeks of persistent COVID-19 disease neither anti-SARS-CoV-2 IgG nor a SARS-CoV-2-specific cellular immune response could be detected, leading to the administration of sotrovimab and remdesivir. Among them, SARS-CoV-2 clearance, detection of IgG, and improvement of graft function were achieved. CONCLUSION: Lack of viral clearance can lead to complications of SARS-CoV-2 infection with atypical manifestations. In kidney transplant patients, before initiating therapy, the differential diagnoses of “rejection” and “virus infection” should be weighed against each other in an interdisciplinary team of nephrologists, infectious diseases specialists and pathologists.
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spelling pubmed-98732062023-01-25 COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report Boss, Kristina Konik, Margarethe Bräsen, Jan Hinrich Schmitz, Jessica Jürgens, Christiane Kribben, Andreas Witzke, Oliver Dolff, Sebastian Gäckler, Anja BMC Nephrol Case Report INTRODUCTION: Immunosuppressive therapy is associated with an increased risk of severe courses of SARS-CoV-2 infection, with frequently delayed viral clearance. We report a case of an acute kidney transplant failure in persistent SARS-CoV-2 infection in a patient with absolute B-cell depletion after administration of rituximab for AB0-incompatible living donor kidney transplantation. CASE PRESENTATION: A 34-year-old unvaccinated patient is diagnosed with SARS-CoV-2 infection four months after kidney transplantation. With only mild symptoms and an estimated glomerular filtration rate (eGFR) of 44 ml/min/1.73 m(2), therapy with molnupiravir was initially given. Within the next eight weeks, transplant biopsies were performed for acute graft failure. These showed acute T-cell rejection with severe acute tubular epithelial damage with only mild interstitial fibrosis and tubular atrophy (BANFF cat. 4 IB), and borderline rejection (BANFF cat. 3). A therapy with prednisolone and intravenous immunoglobulins was performed twice. With unchanged graft failure, the third biopsy also formally showed BANFF cat. 4 IB. However, fluorescence in situ hybridization detected SARS-CoV-2 viruses in large portions of the distal tubules. After nine weeks of persistent COVID-19 disease neither anti-SARS-CoV-2 IgG nor a SARS-CoV-2-specific cellular immune response could be detected, leading to the administration of sotrovimab and remdesivir. Among them, SARS-CoV-2 clearance, detection of IgG, and improvement of graft function were achieved. CONCLUSION: Lack of viral clearance can lead to complications of SARS-CoV-2 infection with atypical manifestations. In kidney transplant patients, before initiating therapy, the differential diagnoses of “rejection” and “virus infection” should be weighed against each other in an interdisciplinary team of nephrologists, infectious diseases specialists and pathologists. BioMed Central 2023-01-24 /pmc/articles/PMC9873206/ /pubmed/36694123 http://dx.doi.org/10.1186/s12882-023-03070-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Boss, Kristina
Konik, Margarethe
Bräsen, Jan Hinrich
Schmitz, Jessica
Jürgens, Christiane
Kribben, Andreas
Witzke, Oliver
Dolff, Sebastian
Gäckler, Anja
COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report
title COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report
title_full COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report
title_fullStr COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report
title_full_unstemmed COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report
title_short COVID-19 associated acute transplant failure after AB0-incompatible living donor kidney transplantation – a case report
title_sort covid-19 associated acute transplant failure after ab0-incompatible living donor kidney transplantation – a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873206/
https://www.ncbi.nlm.nih.gov/pubmed/36694123
http://dx.doi.org/10.1186/s12882-023-03070-z
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