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Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure

BACKGROUND: Cases of H1N1 and other pulmonary infections evolve to acute respiratory failure and death when co‐infections or lung injury predominate over the immune response, thus requiring early diagnosis to improve treatment. OBJECTIVE: To perform a detailed histopathological analysis of the open...

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Autores principales: Capelozzi, Vera Luiza, Parra, Edwin Roger, Ximenes, Manoel, Bammann, Ricardo Helbert, Barbas, Carmen Silvia Valente, Duarte, Marid Irmd Seixas
Formato: Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3020331/
https://www.ncbi.nlm.nih.gov/pubmed/21340209
http://dx.doi.org/10.1590/S1807-59322010001200003
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author Capelozzi, Vera Luiza
Parra, Edwin Roger
Ximenes, Manoel
Bammann, Ricardo Helbert
Barbas, Carmen Silvia Valente
Duarte, Marid Irmd Seixas
author_facet Capelozzi, Vera Luiza
Parra, Edwin Roger
Ximenes, Manoel
Bammann, Ricardo Helbert
Barbas, Carmen Silvia Valente
Duarte, Marid Irmd Seixas
author_sort Capelozzi, Vera Luiza
collection PubMed
description BACKGROUND: Cases of H1N1 and other pulmonary infections evolve to acute respiratory failure and death when co‐infections or lung injury predominate over the immune response, thus requiring early diagnosis to improve treatment. OBJECTIVE: To perform a detailed histopathological analysis of the open lung biopsy specimens from five patients with ARDS with confirmed H1N1. METHODS: Lung specimens underwent microbiologic analysis, and examination by optical and electron microscopy. Immunophenotyping was used to characterize macrophages, natural killer, T and B cells, and expression of cytokines and iNOS. RESULTS: The pathological features observed were necrotizing bronchiolitis, diffuse alveolar damage, alveolar hemorrhage and abnormal immune response. Ultrastructural analysis showed viral‐like particles in all cases. CONCLUSIONS: Viral‐like particles can be successfully demonstrated in lung tissue by ultrastructural examination, without confirmation of the virus by RT‐PCR on nasopharyngeal aspirates. Bronchioles and epithelium, rather than endothelium, are probably the primary target of infection, and diffuse alveolar damage the consequence of the effect of airways obliteration and dysfunction on innate immunity, suggesting that treatment should be focused on epithelial repair.
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spelling pubmed-30203312011-01-16 Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure Capelozzi, Vera Luiza Parra, Edwin Roger Ximenes, Manoel Bammann, Ricardo Helbert Barbas, Carmen Silvia Valente Duarte, Marid Irmd Seixas Clinics (Sao Paulo) Clinical Science BACKGROUND: Cases of H1N1 and other pulmonary infections evolve to acute respiratory failure and death when co‐infections or lung injury predominate over the immune response, thus requiring early diagnosis to improve treatment. OBJECTIVE: To perform a detailed histopathological analysis of the open lung biopsy specimens from five patients with ARDS with confirmed H1N1. METHODS: Lung specimens underwent microbiologic analysis, and examination by optical and electron microscopy. Immunophenotyping was used to characterize macrophages, natural killer, T and B cells, and expression of cytokines and iNOS. RESULTS: The pathological features observed were necrotizing bronchiolitis, diffuse alveolar damage, alveolar hemorrhage and abnormal immune response. Ultrastructural analysis showed viral‐like particles in all cases. CONCLUSIONS: Viral‐like particles can be successfully demonstrated in lung tissue by ultrastructural examination, without confirmation of the virus by RT‐PCR on nasopharyngeal aspirates. Bronchioles and epithelium, rather than endothelium, are probably the primary target of infection, and diffuse alveolar damage the consequence of the effect of airways obliteration and dysfunction on innate immunity, suggesting that treatment should be focused on epithelial repair. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2010-12 /pmc/articles/PMC3020331/ /pubmed/21340209 http://dx.doi.org/10.1590/S1807-59322010001200003 Text en Copyright © 2010 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Capelozzi, Vera Luiza
Parra, Edwin Roger
Ximenes, Manoel
Bammann, Ricardo Helbert
Barbas, Carmen Silvia Valente
Duarte, Marid Irmd Seixas
Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure
title Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure
title_full Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure
title_fullStr Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure
title_full_unstemmed Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure
title_short Pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type A/H1N1 and acute respiratory failure
title_sort pathological and ultrastructural analysis of surgical lung biopsies in patients with swine‐origin influenza type a/h1n1 and acute respiratory failure
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3020331/
https://www.ncbi.nlm.nih.gov/pubmed/21340209
http://dx.doi.org/10.1590/S1807-59322010001200003
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