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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nickan Research Institute
2015
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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. |
format | Online Article Text |
id | pubmed-4827379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nickan Research Institute |
record_format | MEDLINE/PubMed |
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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