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Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies

Allogeneic hematopoietic stem cell transplantation (HSCT) is an effective therapy for patients with hematologic malignancies. Severe pneumonia is associated with high mortality rate in HSCT recipients. Viral co-infection indicates a poor prognosis of HSCT recipients. In this study, a total of 68 all...

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Autores principales: Yue, Caifeng, Kang, ZhiJie, Ai, Kexin, Xu, Duorong, Wu, Jim, Pan, Yujia, Yan, JinSong, Liu, Min, Liu, Quentin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288233/
https://www.ncbi.nlm.nih.gov/pubmed/27340772
http://dx.doi.org/10.18632/oncotarget.10182
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author Yue, Caifeng
Kang, ZhiJie
Ai, Kexin
Xu, Duorong
Wu, Jim
Pan, Yujia
Yan, JinSong
Liu, Min
Liu, Quentin
author_facet Yue, Caifeng
Kang, ZhiJie
Ai, Kexin
Xu, Duorong
Wu, Jim
Pan, Yujia
Yan, JinSong
Liu, Min
Liu, Quentin
author_sort Yue, Caifeng
collection PubMed
description Allogeneic hematopoietic stem cell transplantation (HSCT) is an effective therapy for patients with hematologic malignancies. Severe pneumonia is associated with high mortality rate in HSCT recipients. Viral co-infection indicates a poor prognosis of HSCT recipients. In this study, a total of 68 allogeneic HSCT recipients were included. Cytomegalovirus (CMV) and Respiratory syncytial virus (RSV) infection was assessed by testing peripheral blood and oropharynx swabs, respectively, collected in the first 180 days after transplantation. We analysed the correlation of CMV and RSV co-infection with severe pneumonia and mortality. The incidence of CMV and RSV co-infection was 26.5% (18/68). Severe pneumonia was diagnosed in 61% (11/18) cases with co-infection compared to only 10% (5/50) cases with mono-infection or no infection. The analysis of potential risk factors for severe pneumonia showed that CMV and RSV co-infection was significantly associated with severe pneumonia (p < 0.001). The 5 patients who died of severe pneumonia were all co-infected with CMV and RSV. In conclusion, CMV and RSV co-infection appears to be an important factor and facilitates the development of severe pneumonia in allogeneic HSCT patients with hematologic malignancies.
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spelling pubmed-52882332017-02-07 Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies Yue, Caifeng Kang, ZhiJie Ai, Kexin Xu, Duorong Wu, Jim Pan, Yujia Yan, JinSong Liu, Min Liu, Quentin Oncotarget Clinical Research Paper Allogeneic hematopoietic stem cell transplantation (HSCT) is an effective therapy for patients with hematologic malignancies. Severe pneumonia is associated with high mortality rate in HSCT recipients. Viral co-infection indicates a poor prognosis of HSCT recipients. In this study, a total of 68 allogeneic HSCT recipients were included. Cytomegalovirus (CMV) and Respiratory syncytial virus (RSV) infection was assessed by testing peripheral blood and oropharynx swabs, respectively, collected in the first 180 days after transplantation. We analysed the correlation of CMV and RSV co-infection with severe pneumonia and mortality. The incidence of CMV and RSV co-infection was 26.5% (18/68). Severe pneumonia was diagnosed in 61% (11/18) cases with co-infection compared to only 10% (5/50) cases with mono-infection or no infection. The analysis of potential risk factors for severe pneumonia showed that CMV and RSV co-infection was significantly associated with severe pneumonia (p < 0.001). The 5 patients who died of severe pneumonia were all co-infected with CMV and RSV. In conclusion, CMV and RSV co-infection appears to be an important factor and facilitates the development of severe pneumonia in allogeneic HSCT patients with hematologic malignancies. Impact Journals LLC 2016-06-20 /pmc/articles/PMC5288233/ /pubmed/27340772 http://dx.doi.org/10.18632/oncotarget.10182 Text en Copyright: © 2016 Yue et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Yue, Caifeng
Kang, ZhiJie
Ai, Kexin
Xu, Duorong
Wu, Jim
Pan, Yujia
Yan, JinSong
Liu, Min
Liu, Quentin
Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
title Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
title_full Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
title_fullStr Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
title_full_unstemmed Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
title_short Virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
title_sort virus infection facilitates the development of severe pneumonia in transplant patients with hematologic malignancies
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288233/
https://www.ncbi.nlm.nih.gov/pubmed/27340772
http://dx.doi.org/10.18632/oncotarget.10182
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