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Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction
BACKGROUND: Metapneumoviral respiratory infection is a community-acquired respiratory viral (CARV) infection. Lung transplantation recipients exposed to CARV are at risk for development of allograft rejection. The cellular and molecular pathways initiated by viral infection leading to allograft dysf...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373596/ https://www.ncbi.nlm.nih.gov/pubmed/25848314 http://dx.doi.org/10.2147/JIR.S78259 |
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author | Dosanjh, Amrita |
author_facet | Dosanjh, Amrita |
author_sort | Dosanjh, Amrita |
collection | PubMed |
description | BACKGROUND: Metapneumoviral respiratory infection is a community-acquired respiratory viral (CARV) infection. Lung transplantation recipients exposed to CARV are at risk for development of allograft rejection. The cellular and molecular pathways initiated by viral infection leading to allograft dysfunction are not completely understood. The aim of this study was to identify human metapneumoviral (hMPV) cases in association with allograft rejection. METHODS: A literature search was conducted to identify cases of both hMPV and allograft rejection within 6 months of the initial infection. This resulted in 1,007 lung transplantation recipients, with a total of 2,883 samples identified. Of these, 57 demonstrated isolated hMPV without co-infection with other agents. RESULTS: The results of the study indicate that 35% of acute hMPV infections without co-infection, at the time of detection by molecular diagnostic platforms, were associated with acute cellular rejection within 3 months. There were 9.4% of the cases subsequently associated with chronic allograft dysfunction/bronchiolitis obliterans syndrome, which was collectively termed chronic rejection for purposes of analysis. In conclusion, the prompt identification of isolated hMPV from lung transplantation patients is an important treatable risk factor for subsequent allograft dysfunction. The cellular and molecular pathogenesis of viral-induced allograft rejection remains a topic of future study. |
format | Online Article Text |
id | pubmed-4373596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43735962015-04-06 Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction Dosanjh, Amrita J Inflamm Res Original Research BACKGROUND: Metapneumoviral respiratory infection is a community-acquired respiratory viral (CARV) infection. Lung transplantation recipients exposed to CARV are at risk for development of allograft rejection. The cellular and molecular pathways initiated by viral infection leading to allograft dysfunction are not completely understood. The aim of this study was to identify human metapneumoviral (hMPV) cases in association with allograft rejection. METHODS: A literature search was conducted to identify cases of both hMPV and allograft rejection within 6 months of the initial infection. This resulted in 1,007 lung transplantation recipients, with a total of 2,883 samples identified. Of these, 57 demonstrated isolated hMPV without co-infection with other agents. RESULTS: The results of the study indicate that 35% of acute hMPV infections without co-infection, at the time of detection by molecular diagnostic platforms, were associated with acute cellular rejection within 3 months. There were 9.4% of the cases subsequently associated with chronic allograft dysfunction/bronchiolitis obliterans syndrome, which was collectively termed chronic rejection for purposes of analysis. In conclusion, the prompt identification of isolated hMPV from lung transplantation patients is an important treatable risk factor for subsequent allograft dysfunction. The cellular and molecular pathogenesis of viral-induced allograft rejection remains a topic of future study. Dove Medical Press 2015-03-19 /pmc/articles/PMC4373596/ /pubmed/25848314 http://dx.doi.org/10.2147/JIR.S78259 Text en © 2015 Dosanjh. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Dosanjh, Amrita Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
title | Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
title_full | Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
title_fullStr | Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
title_full_unstemmed | Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
title_short | Respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
title_sort | respiratory metapneumoviral infection without co-infection in association with acute and chronic lung allograft dysfunction |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373596/ https://www.ncbi.nlm.nih.gov/pubmed/25848314 http://dx.doi.org/10.2147/JIR.S78259 |
work_keys_str_mv | AT dosanjhamrita respiratorymetapneumoviralinfectionwithoutcoinfectioninassociationwithacuteandchroniclungallograftdysfunction |