Fms-Like tyrosine kinase-3 ligand attenuates local and systemic infection in a model of post-burn pneumonia

Background: - Burn injury induces immunosuppression and promotes infection with opportunistic pathogens. Pneumonia and sepsis are leading causes of post-burn morbidity and mortality. Fms-like tyrosine kinase-3 ligand (Flt3L) improves local and systemic resistance to P aeruginosa-associated...

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Hauptverfasser: Hundeshagen, Gabriel (VerfasserIn) , Cui, Weihua (VerfasserIn) , Musgrove, Lindsay (VerfasserIn) , Cherry, Aaron (VerfasserIn) , Lee, Seung-Jin (VerfasserIn) , Cox, Robert A. (VerfasserIn) , Toliver-Kinsky, Tracy (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: June 2018
In: Shock
Year: 2018, Jahrgang: 49, Heft: 6, Pages: 721-727
ISSN:1540-0514
DOI:10.1097/SHK.0000000000000964
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1097/SHK.0000000000000964
Verlag, lizenzpflichtig, Volltext: https://journals.lww.com/shockjournal/Fulltext/2018/06000/Fms_Like_Tyrosine_Kinase_3_Ligand_Attenuates_Local.15.aspx
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Verfasserangaben:Gabriel Hundeshagen, Weihua Cui, Lindsay Musgrove, Aaron Cherry, Seung-Jin Lee, Robert A. Cox, and Tracy Toliver-Kinsky
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Zusammenfassung:Background: - Burn injury induces immunosuppression and promotes infection with opportunistic pathogens. Pneumonia and sepsis are leading causes of post-burn morbidity and mortality. Fms-like tyrosine kinase-3 ligand (Flt3L) improves local and systemic resistance to P aeruginosa-associated burn wound infection. This study evaluates the effects of post-burn prophylactic Flt3L treatment on local and systemic infection and inflammation in a murine model of pneumonia and sepsis. - Methods: - Mice received a severe scald burn, were treated with Flt3L or vehicle (CTR) for 5 days, and inoculated trans-nasally with P aeruginosa. Lung, blood, and spleen were harvested at 24 and 48 h postinoculation (p.i.) to assess infection (bacterial burden, bacteremia, distant organ manifestation) and inflammation (interleukin-6 (IL-6) and myeloperoxidase (MPO) levels). Histology correlated infection and inflammation parameters with morphology. Survival at various bacterial concentrations was monitored for 14 days p.i. - Results: - Bacterial burden was significantly reduced in lung and spleen of Flt3L-treated mice. Flt3L treatment was associated with decreased signs of pulmonary inflammation (reduced wet weight and IL-6 levels), lower incidences of bacteremia and septic distant organ manifestation, and reduced systemic inflammation (IL-6 and MPO). Histologically, reduced alveolar and peribronchiolar neutrophil and lymphocyte infiltration indicated attenuated pulmonary inflammation after Flt3L treatment. Overall survival was comparable between groups for all doses of P aeruginosa, but mortality delayed in the Flt3L-treated group. - Conclusion: - Prophylactic treatment with Flt3L could augment antimicrobial therapy of post-burn pneumonia through improvement of the initial host response to challenge with P aeruginosa, attenuate local, and systemic inflammation as well as septic pathogen dissemination.
Beschreibung:Gesehen am 30.04.2020
Beschreibung:Online Resource
ISSN:1540-0514
DOI:10.1097/SHK.0000000000000964