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BK virus nephropathy is not always alone

Introduction: BK virus associated allograft nephropathy (BKVAN) is an important cause of allograft lost that often occurs in the first year of transplantation. The state of over immunosuppression also predispose these patients to various opportunistic viral infection Objectives: This research aimed...

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Autores principales: Esmaili, Haydarali, Mostafidi, Elmira, Ardalan, Mohammadreza, Vahedi, Amir, Mahmoodpoor, Fariba, Mohajel-Shoja, Mohammadali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nickan Research Institute 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827379/
https://www.ncbi.nlm.nih.gov/pubmed/27069959
http://dx.doi.org/10.15171/jrip.2016.03
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author Esmaili, Haydarali
Mostafidi, Elmira
Ardalan, Mohammadreza
Vahedi, Amir
Mahmoodpoor, Fariba
Mohajel-Shoja, Mohammadali
author_facet Esmaili, Haydarali
Mostafidi, Elmira
Ardalan, Mohammadreza
Vahedi, Amir
Mahmoodpoor, Fariba
Mohajel-Shoja, Mohammadali
author_sort Esmaili, Haydarali
collection PubMed
description Introduction: BK virus associated allograft nephropathy (BKVAN) is an important cause of allograft lost that often occurs in the first year of transplantation. The state of over immunosuppression also predispose these patients to various opportunistic viral infection Objectives: This research aimed to study the renal transplanted patients for BK viremia and BKVAN. Patients and methods: This observational study was conducted between January 2013 to December 2014 to study the renal transplanted patients for BK viremia and BKVAN. In our center patients received combination of de-sensitization therapy including antithymocyte globulin (ATG), rituximab (RITU), basiliximab, therapeutic plasma exchange, and methylprednisolone (MTP), in high risks or only MTP therapy in immunologically low risk patients. Results: Of total number of 26 patients (20-52 years, M/F 17/9), seven patients received ATG and seven patient received intensive desensitizing protocols, BKVAN and BK viremia happened in three and two patients in above groups subsequently, only one patient developed BKVAN in low risk group. We also observed; cytomegalovirus (CMV) and parvovirus B19 infection and hemophagocytic syndrome (HPS), thrombotic microangiopathy (TMA) and endocarditis in our patients with BKVAN and BK viremia. Conclusion: Awareness about the possibility of BK virus nephropathy and appropriate immunosuppression minimization are crucial components of management. Consideration of other opportunistic infections and specific syndromes are also very important.
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spelling pubmed-48273792016-04-11 BK virus nephropathy is not always alone Esmaili, Haydarali Mostafidi, Elmira Ardalan, Mohammadreza Vahedi, Amir Mahmoodpoor, Fariba Mohajel-Shoja, Mohammadali J Renal Inj Prev Original Article Introduction: BK virus associated allograft nephropathy (BKVAN) is an important cause of allograft lost that often occurs in the first year of transplantation. The state of over immunosuppression also predispose these patients to various opportunistic viral infection Objectives: This research aimed to study the renal transplanted patients for BK viremia and BKVAN. Patients and methods: This observational study was conducted between January 2013 to December 2014 to study the renal transplanted patients for BK viremia and BKVAN. In our center patients received combination of de-sensitization therapy including antithymocyte globulin (ATG), rituximab (RITU), basiliximab, therapeutic plasma exchange, and methylprednisolone (MTP), in high risks or only MTP therapy in immunologically low risk patients. Results: Of total number of 26 patients (20-52 years, M/F 17/9), seven patients received ATG and seven patient received intensive desensitizing protocols, BKVAN and BK viremia happened in three and two patients in above groups subsequently, only one patient developed BKVAN in low risk group. We also observed; cytomegalovirus (CMV) and parvovirus B19 infection and hemophagocytic syndrome (HPS), thrombotic microangiopathy (TMA) and endocarditis in our patients with BKVAN and BK viremia. Conclusion: Awareness about the possibility of BK virus nephropathy and appropriate immunosuppression minimization are crucial components of management. Consideration of other opportunistic infections and specific syndromes are also very important. Nickan Research Institute 2015-04-24 /pmc/articles/PMC4827379/ /pubmed/27069959 http://dx.doi.org/10.15171/jrip.2016.03 Text en Copyright © 2016 The Author(s); Published by Nickan Research Institute http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Esmaili, Haydarali
Mostafidi, Elmira
Ardalan, Mohammadreza
Vahedi, Amir
Mahmoodpoor, Fariba
Mohajel-Shoja, Mohammadali
BK virus nephropathy is not always alone
title BK virus nephropathy is not always alone
title_full BK virus nephropathy is not always alone
title_fullStr BK virus nephropathy is not always alone
title_full_unstemmed BK virus nephropathy is not always alone
title_short BK virus nephropathy is not always alone
title_sort bk virus nephropathy is not always alone
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827379/
https://www.ncbi.nlm.nih.gov/pubmed/27069959
http://dx.doi.org/10.15171/jrip.2016.03
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