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Infectious Triggers of Chronic Lung Allograft Dysfunction

Survival after lung transplantation is limited in large part due to the high incidence of chronic rejection, known as chronic lung allograft dysfunction (CLAD). Pulmonary infections are a frequent complication in lung transplant recipients, due both to immunosuppressive medications and constant expo...

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Detalles Bibliográficos
Autor principal: Gregson, Aric L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089243/
https://www.ncbi.nlm.nih.gov/pubmed/27221821
http://dx.doi.org/10.1007/s11908-016-0529-6
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author Gregson, Aric L.
author_facet Gregson, Aric L.
author_sort Gregson, Aric L.
collection PubMed
description Survival after lung transplantation is limited in large part due to the high incidence of chronic rejection, known as chronic lung allograft dysfunction (CLAD). Pulmonary infections are a frequent complication in lung transplant recipients, due both to immunosuppressive medications and constant exposure of the lung allograft to the external environment via the airways. Infection is a recognized risk factor for the development of CLAD, and both acute infection and chronic lung allograft colonization with microorganisms increase the risk for CLAD. Acute infection by community acquired respiratory viruses, and the bacteria Pseudomonas aeruginosa and Staphylococcus aureus are increasingly recognized as important risk factors for CLAD. Colonization by the fungus Aspergillus may also augment the risk of CLAD. Fostering this transition from healthy lung to CLAD in each of these infectious episodes is the persistence of an inflammatory lung allograft environment.
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spelling pubmed-70892432020-03-23 Infectious Triggers of Chronic Lung Allograft Dysfunction Gregson, Aric L. Curr Infect Dis Rep Transplant and Oncology (M Ison, N Theodoropoulos and S Pegram, Section Editors) Survival after lung transplantation is limited in large part due to the high incidence of chronic rejection, known as chronic lung allograft dysfunction (CLAD). Pulmonary infections are a frequent complication in lung transplant recipients, due both to immunosuppressive medications and constant exposure of the lung allograft to the external environment via the airways. Infection is a recognized risk factor for the development of CLAD, and both acute infection and chronic lung allograft colonization with microorganisms increase the risk for CLAD. Acute infection by community acquired respiratory viruses, and the bacteria Pseudomonas aeruginosa and Staphylococcus aureus are increasingly recognized as important risk factors for CLAD. Colonization by the fungus Aspergillus may also augment the risk of CLAD. Fostering this transition from healthy lung to CLAD in each of these infectious episodes is the persistence of an inflammatory lung allograft environment. Springer US 2016-05-24 2016 /pmc/articles/PMC7089243/ /pubmed/27221821 http://dx.doi.org/10.1007/s11908-016-0529-6 Text en © Springer Science+Business Media New York 2016 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Transplant and Oncology (M Ison, N Theodoropoulos and S Pegram, Section Editors)
Gregson, Aric L.
Infectious Triggers of Chronic Lung Allograft Dysfunction
title Infectious Triggers of Chronic Lung Allograft Dysfunction
title_full Infectious Triggers of Chronic Lung Allograft Dysfunction
title_fullStr Infectious Triggers of Chronic Lung Allograft Dysfunction
title_full_unstemmed Infectious Triggers of Chronic Lung Allograft Dysfunction
title_short Infectious Triggers of Chronic Lung Allograft Dysfunction
title_sort infectious triggers of chronic lung allograft dysfunction
topic Transplant and Oncology (M Ison, N Theodoropoulos and S Pegram, Section Editors)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089243/
https://www.ncbi.nlm.nih.gov/pubmed/27221821
http://dx.doi.org/10.1007/s11908-016-0529-6
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