HMGB1 signaling blocking protects against carbapenem-resistant klebsiella pneumoniae in a murine model of infection.

Abstract:

PURPOSE OF THE STUDY:Pulmonary infection with Klebsiella pneumoniae (KP) and carbapenem-resistant Klebsiella pneumoniae (CRKP) significantly contribute to morbidity and mortality in pneumonia. Recent studies have indicated that High-Mobility Group Box 1 Protein (HMGB1) plays an important role in the prevention and treatment of pneumonia. However the role of HMGB1 in CRKP-induced pneumonia has not been addressed. Materials andMethods: In vivo, we successfully established the KP and CRKP-induced pneumonia mouse model. We then tested the anti-HMGB1 IgG prevents CRKP-induced pneumonia. RESULTS:The mice treated with the anti-HMGB1 IgG ameliorated CRKP-induced pulmonary infiltration of inflammatory cells, dissemination of bacteria and the cytokine storm by suppressing the HMGB1 signaling pathways. CONCLUSION:These results indicate that HMGB1 may be an important contributor in these changes of CRKP-induced pneumonia. Thus, HMGB1 may provide a therapeutic target for reducing bacterial infection and lung inflammation in CRKP pneumonia.

journal_name

Exp Lung Res

authors

Liming S,Guixia L,Wenxin S,Guirong T

doi

10.1080/01902148.2018.1505976

subject

Has Abstract

pub_date

2018-08-01 00:00:00

pages

263-271

issue

6

eissn

0190-2148

issn

1521-0499

journal_volume

44

pub_type

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