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CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection
Klebsiella pneumoniae-associated pathology is largely mediated by neutrophilic inflammation. In this study, we administered Klebsiella pneumoniae to experimental guinea pig groups and the ELR-CXC chemokine antagonist CXCL8((3–72)), ceftazidime, and dexamethasone to different groups, respectively. Af...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613076/ https://www.ncbi.nlm.nih.gov/pubmed/23586055 http://dx.doi.org/10.1155/2013/720975 |
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author | Wei, Jing Peng, Jing Wang, Bing Qu, Hong Wang, Shiyi Faisal, Aziz Cheng, Jia-Wei Gordon, John R. Li, Fang |
author_facet | Wei, Jing Peng, Jing Wang, Bing Qu, Hong Wang, Shiyi Faisal, Aziz Cheng, Jia-Wei Gordon, John R. Li, Fang |
author_sort | Wei, Jing |
collection | PubMed |
description | Klebsiella pneumoniae-associated pathology is largely mediated by neutrophilic inflammation. In this study, we administered Klebsiella pneumoniae to experimental guinea pig groups and the ELR-CXC chemokine antagonist CXCL8((3–72)), ceftazidime, and dexamethasone to different groups, respectively. After 24 h, we assessed the animal's pulmonary inflammatory levels, including gross histopathology, airway neutrophilia, lung myeloperoxidase levels, expressions of CXCL8 and TNF, and airway bacterial loads. Compared with ceftazidime and dexamethasone treatments, the administration of the ELR-CXC chemokine antagonist CXCL8((3–72)) alone was more effective than other methods, although it did not markedly attenuate the bacterial load. These results suggest new methods for the treatment of Klebsiella pneumoniae pathology. |
format | Online Article Text |
id | pubmed-3613076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36130762013-04-12 CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection Wei, Jing Peng, Jing Wang, Bing Qu, Hong Wang, Shiyi Faisal, Aziz Cheng, Jia-Wei Gordon, John R. Li, Fang Biomed Res Int Research Article Klebsiella pneumoniae-associated pathology is largely mediated by neutrophilic inflammation. In this study, we administered Klebsiella pneumoniae to experimental guinea pig groups and the ELR-CXC chemokine antagonist CXCL8((3–72)), ceftazidime, and dexamethasone to different groups, respectively. After 24 h, we assessed the animal's pulmonary inflammatory levels, including gross histopathology, airway neutrophilia, lung myeloperoxidase levels, expressions of CXCL8 and TNF, and airway bacterial loads. Compared with ceftazidime and dexamethasone treatments, the administration of the ELR-CXC chemokine antagonist CXCL8((3–72)) alone was more effective than other methods, although it did not markedly attenuate the bacterial load. These results suggest new methods for the treatment of Klebsiella pneumoniae pathology. Hindawi Publishing Corporation 2013 2013-03-18 /pmc/articles/PMC3613076/ /pubmed/23586055 http://dx.doi.org/10.1155/2013/720975 Text en Copyright © 2013 Jing Wei et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wei, Jing Peng, Jing Wang, Bing Qu, Hong Wang, Shiyi Faisal, Aziz Cheng, Jia-Wei Gordon, John R. Li, Fang CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection |
title | CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection |
title_full | CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection |
title_fullStr | CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection |
title_full_unstemmed | CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection |
title_short | CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection |
title_sort | cxcr1/cxcr2 antagonism is effective in pulmonary defense against klebsiella pneumoniae infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613076/ https://www.ncbi.nlm.nih.gov/pubmed/23586055 http://dx.doi.org/10.1155/2013/720975 |
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