Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection. / Calum, Henrik Pierre; Moser, Claus Ernst; Jensen, Peter Østrup; Christoffersen, L.; Damlund, Dina Silke Malling; Alhede, Maria; Bjarnsholt, Thomas; Hougen, Hans Petter; Givskov, Michael; Jacobsen, Grete Krag; Høiby, Niels.

In: Clinical and Experimental Immunology, Vol. 156, No. 1, 2008, p. 102-110.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Calum, HP, Moser, CE, Jensen, PØ, Christoffersen, L, Damlund, DSM, Alhede, M, Bjarnsholt, T, Hougen, HP, Givskov, M, Jacobsen, GK & Høiby, N 2008, 'Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection', Clinical and Experimental Immunology, vol. 156, no. 1, pp. 102-110. https://doi.org/10.1111/j.1365-2249.2008.03861.x

APA

Calum, H. P., Moser, C. E., Jensen, P. Ø., Christoffersen, L., Damlund, D. S. M., Alhede, M., Bjarnsholt, T., Hougen, H. P., Givskov, M., Jacobsen, G. K., & Høiby, N. (2008). Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection. Clinical and Experimental Immunology, 156(1), 102-110. https://doi.org/10.1111/j.1365-2249.2008.03861.x

Vancouver

Calum HP, Moser CE, Jensen PØ, Christoffersen L, Damlund DSM, Alhede M et al. Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection. Clinical and Experimental Immunology. 2008;156(1):102-110. https://doi.org/10.1111/j.1365-2249.2008.03861.x

Author

Calum, Henrik Pierre ; Moser, Claus Ernst ; Jensen, Peter Østrup ; Christoffersen, L. ; Damlund, Dina Silke Malling ; Alhede, Maria ; Bjarnsholt, Thomas ; Hougen, Hans Petter ; Givskov, Michael ; Jacobsen, Grete Krag ; Høiby, Niels. / Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection. In: Clinical and Experimental Immunology. 2008 ; Vol. 156, No. 1. pp. 102-110.

Bibtex

@article{79443cb0fcdd11ddb219000ea68e967b,
title = "Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection",
abstract = "Severe thermal injury induces immunosuppression, involving all parts of the immune system, especially when large fractions of the total body surface area are affected. An animal model was established to characterize the burn-induced immunosuppression. In our novel mouse model a 6% third-degree burn injury was induced in mice with a hot-air blower. The third-degree burn was confirmed histologically. The mice were allocated into five groups: control, shave, burn, infection and burn infection group. At 48 h, a decline in the concentration of peripheral blood leucocytes was observed in the group of mice with burn wound. The reduction was ascribed to the decline in concentration of polymorphonuclear neutrophil leucocytes and monocytes. When infecting the skin with Pseudomonas aeruginosa, a dissemination of bacteria was observed only in the burn wound group. Histological characterization of the skin showed a more polymorphonuclear neutrophil granulocytes (PMNs)-dominated inflammation in the group of mice with infected burn wound compared with the with burn wound group. In contrast, a higher degree of inflammation was observed in the burn wound group compared with the group of mice with infected burn wound. Furthermore, the oxidative burst and the phagocytic capacity of the PMNs were reduced in the group of mice with burn wound. Using this novel mouse model of thermal injury a decline of peripheral leucocytes was observed, whereas the increased local inflammatory response at the site of infection showed reduced capacity to contain and eliminate the infection.",
author = "Calum, {Henrik Pierre} and Moser, {Claus Ernst} and Jensen, {Peter {\O}strup} and L. Christoffersen and Damlund, {Dina Silke Malling} and Maria Alhede and Thomas Bjarnsholt and Hougen, {Hans Petter} and Michael Givskov and Jacobsen, {Grete Krag} and Niels H{\o}iby",
year = "2008",
doi = "10.1111/j.1365-2249.2008.03861.x",
language = "English",
volume = "156",
pages = "102--110",
journal = "Clinical and Experimental Immunology, Supplement",
issn = "0964-2536",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Thermal injury induces impaired function in polymorphonuclear neutrophil granulocytes and reduced control of burn wound infection

AU - Calum, Henrik Pierre

AU - Moser, Claus Ernst

AU - Jensen, Peter Østrup

AU - Christoffersen, L.

AU - Damlund, Dina Silke Malling

AU - Alhede, Maria

AU - Bjarnsholt, Thomas

AU - Hougen, Hans Petter

AU - Givskov, Michael

AU - Jacobsen, Grete Krag

AU - Høiby, Niels

PY - 2008

Y1 - 2008

N2 - Severe thermal injury induces immunosuppression, involving all parts of the immune system, especially when large fractions of the total body surface area are affected. An animal model was established to characterize the burn-induced immunosuppression. In our novel mouse model a 6% third-degree burn injury was induced in mice with a hot-air blower. The third-degree burn was confirmed histologically. The mice were allocated into five groups: control, shave, burn, infection and burn infection group. At 48 h, a decline in the concentration of peripheral blood leucocytes was observed in the group of mice with burn wound. The reduction was ascribed to the decline in concentration of polymorphonuclear neutrophil leucocytes and monocytes. When infecting the skin with Pseudomonas aeruginosa, a dissemination of bacteria was observed only in the burn wound group. Histological characterization of the skin showed a more polymorphonuclear neutrophil granulocytes (PMNs)-dominated inflammation in the group of mice with infected burn wound compared with the with burn wound group. In contrast, a higher degree of inflammation was observed in the burn wound group compared with the group of mice with infected burn wound. Furthermore, the oxidative burst and the phagocytic capacity of the PMNs were reduced in the group of mice with burn wound. Using this novel mouse model of thermal injury a decline of peripheral leucocytes was observed, whereas the increased local inflammatory response at the site of infection showed reduced capacity to contain and eliminate the infection.

AB - Severe thermal injury induces immunosuppression, involving all parts of the immune system, especially when large fractions of the total body surface area are affected. An animal model was established to characterize the burn-induced immunosuppression. In our novel mouse model a 6% third-degree burn injury was induced in mice with a hot-air blower. The third-degree burn was confirmed histologically. The mice were allocated into five groups: control, shave, burn, infection and burn infection group. At 48 h, a decline in the concentration of peripheral blood leucocytes was observed in the group of mice with burn wound. The reduction was ascribed to the decline in concentration of polymorphonuclear neutrophil leucocytes and monocytes. When infecting the skin with Pseudomonas aeruginosa, a dissemination of bacteria was observed only in the burn wound group. Histological characterization of the skin showed a more polymorphonuclear neutrophil granulocytes (PMNs)-dominated inflammation in the group of mice with infected burn wound compared with the with burn wound group. In contrast, a higher degree of inflammation was observed in the burn wound group compared with the group of mice with infected burn wound. Furthermore, the oxidative burst and the phagocytic capacity of the PMNs were reduced in the group of mice with burn wound. Using this novel mouse model of thermal injury a decline of peripheral leucocytes was observed, whereas the increased local inflammatory response at the site of infection showed reduced capacity to contain and eliminate the infection.

U2 - 10.1111/j.1365-2249.2008.03861.x

DO - 10.1111/j.1365-2249.2008.03861.x

M3 - Journal article

C2 - 19210518

VL - 156

SP - 102

EP - 110

JO - Clinical and Experimental Immunology, Supplement

JF - Clinical and Experimental Immunology, Supplement

SN - 0964-2536

IS - 1

ER -

ID: 10612742