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Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)

BACKGROUND: Acute viral respiratory infections represent a globally important cause of morbidity and mortality in childhood. An individual's cellular response appears to play a critical role in recovery from infections, given that individuals with impaired cellular immunity, congenital or acqui...

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Autores principales: de Souza Costa, Victor Horácio, Baurakiades, Emanuele, Viola Azevedo, Marina Louise, Traiano, Gabriela, Kowal Rosales, Jeana, Kunze Larsen, Kelly Susana, Raboni, Sonia Maria, de Noronha, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173026/
https://www.ncbi.nlm.nih.gov/pubmed/25052332
http://dx.doi.org/10.1016/j.jcv.2014.06.026
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author de Souza Costa, Victor Horácio
Baurakiades, Emanuele
Viola Azevedo, Marina Louise
Traiano, Gabriela
Kowal Rosales, Jeana
Kunze Larsen, Kelly Susana
Raboni, Sonia Maria
de Noronha, Lucia
author_facet de Souza Costa, Victor Horácio
Baurakiades, Emanuele
Viola Azevedo, Marina Louise
Traiano, Gabriela
Kowal Rosales, Jeana
Kunze Larsen, Kelly Susana
Raboni, Sonia Maria
de Noronha, Lucia
author_sort de Souza Costa, Victor Horácio
collection PubMed
description BACKGROUND: Acute viral respiratory infections represent a globally important cause of morbidity and mortality in childhood. An individual's cellular response appears to play a critical role in recovery from infections, given that individuals with impaired cellular immunity, congenital or acquired, have more severe diseases and secrete the virus for longer periods. OBJECTIVES: The aim of this study was to immunohistochemically evaluate the expression of the cell surface antigens CD4, CD8, CD25, CD14 and CD74, in pneumonic infiltrates in the alveolar septa using paraffin-embedded lung samples from autopsies of immunocompetent children who died of lethal, non-pandemic, severe acute respiratory infections. STUDY DESIGN: From 794 cases of pediatric autopsies of patients with severe respiratory disease (between 1960 and 2004), 193 cases were selected for this study. To identify subpopulations of inflammatory cells in the alveolar septa, cell surface antigen expression was assessed by immunohistochemistry using the following primary antibodies: anti-CD4, anti-CD8, anti-CD14, anti-CD25 and anti-CD74. RESULTS: The TCD8+ lymphocyte count was higher in the virus-positive group (p = 0.04) and was also much higher among cases that were positive for more than three viral types (p = 0.016). There were fewer CD14+ cells in cases of AdV (adenovirus) infection (p = 0.002), and there was a predominance of CD74+ cells in the histopathological pattern defined as interstitial pneumonitis (p = 0.037). CONCLUSIONS: The results of this study demonstrate that TCD8+ lymphocytes present in the alveolar septa participate to a greater extent in the response toward viral pneumonia, while CD14+ cell numbers are often reduced in cases of AdV.
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spelling pubmed-71730262020-04-22 Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B) de Souza Costa, Victor Horácio Baurakiades, Emanuele Viola Azevedo, Marina Louise Traiano, Gabriela Kowal Rosales, Jeana Kunze Larsen, Kelly Susana Raboni, Sonia Maria de Noronha, Lucia J Clin Virol Article BACKGROUND: Acute viral respiratory infections represent a globally important cause of morbidity and mortality in childhood. An individual's cellular response appears to play a critical role in recovery from infections, given that individuals with impaired cellular immunity, congenital or acquired, have more severe diseases and secrete the virus for longer periods. OBJECTIVES: The aim of this study was to immunohistochemically evaluate the expression of the cell surface antigens CD4, CD8, CD25, CD14 and CD74, in pneumonic infiltrates in the alveolar septa using paraffin-embedded lung samples from autopsies of immunocompetent children who died of lethal, non-pandemic, severe acute respiratory infections. STUDY DESIGN: From 794 cases of pediatric autopsies of patients with severe respiratory disease (between 1960 and 2004), 193 cases were selected for this study. To identify subpopulations of inflammatory cells in the alveolar septa, cell surface antigen expression was assessed by immunohistochemistry using the following primary antibodies: anti-CD4, anti-CD8, anti-CD14, anti-CD25 and anti-CD74. RESULTS: The TCD8+ lymphocyte count was higher in the virus-positive group (p = 0.04) and was also much higher among cases that were positive for more than three viral types (p = 0.016). There were fewer CD14+ cells in cases of AdV (adenovirus) infection (p = 0.002), and there was a predominance of CD74+ cells in the histopathological pattern defined as interstitial pneumonitis (p = 0.037). CONCLUSIONS: The results of this study demonstrate that TCD8+ lymphocytes present in the alveolar septa participate to a greater extent in the response toward viral pneumonia, while CD14+ cell numbers are often reduced in cases of AdV. Elsevier B.V. 2014-10 2014-07-03 /pmc/articles/PMC7173026/ /pubmed/25052332 http://dx.doi.org/10.1016/j.jcv.2014.06.026 Text en Copyright © 2014 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
de Souza Costa, Victor Horácio
Baurakiades, Emanuele
Viola Azevedo, Marina Louise
Traiano, Gabriela
Kowal Rosales, Jeana
Kunze Larsen, Kelly Susana
Raboni, Sonia Maria
de Noronha, Lucia
Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)
title Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)
title_full Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)
title_fullStr Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)
title_full_unstemmed Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)
title_short Immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (RSV; ADV; PIV1; PIV2; PIV3; FLU A; FLU B)
title_sort immunohistochemistry analysis of pulmonary infiltrates in necropsy samples of children with non-pandemic lethal respiratory infections (rsv; adv; piv1; piv2; piv3; flu a; flu b)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173026/
https://www.ncbi.nlm.nih.gov/pubmed/25052332
http://dx.doi.org/10.1016/j.jcv.2014.06.026
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