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Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice
BACKGROUND: Acinetobacter baumannii (A. baumannii) has become one of the most important opportunistic pathogens inducing nosocomial pneumonia and increasing mortality in critically ill patients recently. The interaction between A. baumannii infection and immune response can influence the prognosis o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508442/ https://www.ncbi.nlm.nih.gov/pubmed/32842019 http://dx.doi.org/10.1097/CM9.0000000000001027 |
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author | Liu, Ai-Ran Du, Wen-Jing Xie, Jian-Feng Xu, Jing-Yuan Huang, Ying-Zi Qiu, Hai-Bo Yang, Yi |
author_facet | Liu, Ai-Ran Du, Wen-Jing Xie, Jian-Feng Xu, Jing-Yuan Huang, Ying-Zi Qiu, Hai-Bo Yang, Yi |
author_sort | Liu, Ai-Ran |
collection | PubMed |
description | BACKGROUND: Acinetobacter baumannii (A. baumannii) has become one of the most important opportunistic pathogens inducing nosocomial pneumonia and increasing mortality in critically ill patients recently. The interaction between A. baumannii infection and immune response can influence the prognosis of A. baumannii related pneumonia. The target of the present study was to investigate the role of immunodeficiency in A. baumannii induced pneumonia. METHODS: Male BALB/c mice were randomly divided into the normal immunity control (NIC) group, normal immunity infection (NIA) group, immune compromised control (CIC) group, and immune compromised infection (CIA) group (n = 15 for each group). Intraperitoneal injection of cyclophosphamide and intranasal instillation of A. baumannii solution were used to induce compromised immunity and murine pneumonia, respectively. The mice were sacrificed at 6 and 24 h later and the specimens were collected for further tests. Seven-day mortality of mice was also assessed. RESULTS: After A. baumannii stimulation, the recruitment of neutrophils in mice with normal immunity increased sharply (P = 0.030 at 6 h), while there was no significant raise of neutrophil counts in mice with compromised immune condition (P = 0.092 at 6 h, P = 0.772 at 24 h). The Th cell polarization presented with pulmonary interleukin (IL)-4 and interferon (IFN)-γ level in response to the A. baumannii in CIA group were significantly depressed in comparison with in NIA group (IFN-γ: P = 0.003 at 6 h; P = 0.001 at 24 h; IL-4: P < 0.001 at 6 h; P < 0.001 at 24 h). The pulmonary conventional dendritic cell accumulation was even found to be inhibited after A. baumannii infection in immunocompromised mice (P = 0.033). Correspondingly, A. baumannii associated pneumonia in mice with compromised immunity caused more early stage death, more severe histopathological impairment in lung. CONCLUSION: A. baumannii could frustrate the immune response in immunocompromised conditions, and this reduced immune response is related to more severe lung injury and worse outcome in A. baumannii induced pneumonia. |
format | Online Article Text |
id | pubmed-7508442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-75084422020-10-14 Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice Liu, Ai-Ran Du, Wen-Jing Xie, Jian-Feng Xu, Jing-Yuan Huang, Ying-Zi Qiu, Hai-Bo Yang, Yi Chin Med J (Engl) Original Articles BACKGROUND: Acinetobacter baumannii (A. baumannii) has become one of the most important opportunistic pathogens inducing nosocomial pneumonia and increasing mortality in critically ill patients recently. The interaction between A. baumannii infection and immune response can influence the prognosis of A. baumannii related pneumonia. The target of the present study was to investigate the role of immunodeficiency in A. baumannii induced pneumonia. METHODS: Male BALB/c mice were randomly divided into the normal immunity control (NIC) group, normal immunity infection (NIA) group, immune compromised control (CIC) group, and immune compromised infection (CIA) group (n = 15 for each group). Intraperitoneal injection of cyclophosphamide and intranasal instillation of A. baumannii solution were used to induce compromised immunity and murine pneumonia, respectively. The mice were sacrificed at 6 and 24 h later and the specimens were collected for further tests. Seven-day mortality of mice was also assessed. RESULTS: After A. baumannii stimulation, the recruitment of neutrophils in mice with normal immunity increased sharply (P = 0.030 at 6 h), while there was no significant raise of neutrophil counts in mice with compromised immune condition (P = 0.092 at 6 h, P = 0.772 at 24 h). The Th cell polarization presented with pulmonary interleukin (IL)-4 and interferon (IFN)-γ level in response to the A. baumannii in CIA group were significantly depressed in comparison with in NIA group (IFN-γ: P = 0.003 at 6 h; P = 0.001 at 24 h; IL-4: P < 0.001 at 6 h; P < 0.001 at 24 h). The pulmonary conventional dendritic cell accumulation was even found to be inhibited after A. baumannii infection in immunocompromised mice (P = 0.033). Correspondingly, A. baumannii associated pneumonia in mice with compromised immunity caused more early stage death, more severe histopathological impairment in lung. CONCLUSION: A. baumannii could frustrate the immune response in immunocompromised conditions, and this reduced immune response is related to more severe lung injury and worse outcome in A. baumannii induced pneumonia. Lippincott Williams & Wilkins 2020-09-20 2020-08-24 /pmc/articles/PMC7508442/ /pubmed/32842019 http://dx.doi.org/10.1097/CM9.0000000000001027 Text en Copyright © 2020 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Original Articles Liu, Ai-Ran Du, Wen-Jing Xie, Jian-Feng Xu, Jing-Yuan Huang, Ying-Zi Qiu, Hai-Bo Yang, Yi Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice |
title | Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice |
title_full | Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice |
title_fullStr | Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice |
title_full_unstemmed | Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice |
title_short | Role of immunodeficiency in Acinetobacter baumannii associated pneumonia in mice |
title_sort | role of immunodeficiency in acinetobacter baumannii associated pneumonia in mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7508442/ https://www.ncbi.nlm.nih.gov/pubmed/32842019 http://dx.doi.org/10.1097/CM9.0000000000001027 |
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