CXCR1/CXCR2 Antagonism Is Effective in Pulmonary Defense against Klebsiella pneumoniae Infection

被引:12
|
作者
Wei, Jing [1 ]
Peng, Jing [2 ]
Wang, Bing [1 ]
Qu, Hong [1 ]
Wang, Shiyi [1 ]
Faisal, Aziz [3 ]
Cheng, Jia-Wei [4 ]
Gordon, John R. [5 ]
Li, Fang [1 ]
机构
[1] Dalian Med Univ, Dept Immunol, Dalian 116044, Peoples R China
[2] Karamay Cent Hosp, Dept Clin Lab, Karamay 834000, Peoples R China
[3] Dalian Med Univ, Dept Biochem, Dalian 116044, Peoples R China
[4] Natl Tsing Hua Univ, Inst Biotechnol, Dept Life Sci, Hsinchu 300, Taiwan
[5] Univ Saskatchewan, Royal Univ Hosp, Div Respirol Crit Care & Sleep Med, Saskatoon, SK S7N 0W8, Canada
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
CXC CHEMOKINE ANTAGONISM; NEUTROPHIL RECRUITMENT; PATHOLOGY; ALPHA(4)-INTEGRIN; CORTICOSTEROIDS; INHIBITION; RESPONSES; IL-8;
D O I
10.1155/2013/720975
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页数:6
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