TY - JOUR
T1 - Acute phase response impairs host defense against Pseudomonas aeruginosa pneumonia in mice
AU - Renckens, Rosemarijn
AU - van Westerloo, David J.
AU - Roelofs, Joris J. T. H.
AU - Pater, Jennie M.
AU - Schultz, Marcus J.
AU - Florquin, Sandrine
AU - van der Poll, Tom
PY - 2008
Y1 - 2008
N2 - OBJECTIVE: Pseudomonas aeruginosa is a common pathogen in hospital-acquired pneumonia. Especially trauma and postsurgical patients display a profound acute phase protein response and are susceptible to acquiring pneumonia. The objective was to study the influence of the acute phase response induced by sterile tissue injury on pulmonary host defense. DESIGN: Laboratory investigation. SETTING: Academic medical center. SUBJECTS: Female C57Bl/6 wild-type mice, 8-10 wks old. INTERVENTIONS: Mice were injected subcutaneously with either turpentine or sterile saline (control) in both hind limbs 1 day before intranasal infection with P. aeruginosa. MEASUREMENTS AND MAIN RESULTS: The turpentine-induced acute phase response was associated with 100% lethality after induction of pneumonia, whereas control mice all survived the Pseudomonas infection. In addition, turpentine-injected mice demonstrated much higher bacterial loads in their lungs and an increased dissemination of the infection. The acute phase reaction attenuated lung inflammation during pneumonia, as reflected by histopathology, reduced pulmonary levels of proinflammatory cytokines, and a strongly diminished recruitment of neutrophils to the site of infection. Blood neutrophils harvested from turpentine injected mice displayed a reduced capacity to up-regulate their CD11b/CD18 expression upon stimulation with Pseudomonas ex vivo and during Pseudomonas pneumonia in vivo. Administration of a blocking anti-CD11b antibody to turpentine-injected and control mice almost completely abrogated the difference in bacterial outgrowth, whereas inhibition of the sympathetic nervous system did not affect the impaired pulmonary host defense in mice with an acute phase response. CONCLUSIONS: These data suggest that a systemic acute phase response might impair host defense against P. aeruginosa pneumonia, possibly in part by inhibition of CD11b/CD18-dependent neutrophil recruitment
AB - OBJECTIVE: Pseudomonas aeruginosa is a common pathogen in hospital-acquired pneumonia. Especially trauma and postsurgical patients display a profound acute phase protein response and are susceptible to acquiring pneumonia. The objective was to study the influence of the acute phase response induced by sterile tissue injury on pulmonary host defense. DESIGN: Laboratory investigation. SETTING: Academic medical center. SUBJECTS: Female C57Bl/6 wild-type mice, 8-10 wks old. INTERVENTIONS: Mice were injected subcutaneously with either turpentine or sterile saline (control) in both hind limbs 1 day before intranasal infection with P. aeruginosa. MEASUREMENTS AND MAIN RESULTS: The turpentine-induced acute phase response was associated with 100% lethality after induction of pneumonia, whereas control mice all survived the Pseudomonas infection. In addition, turpentine-injected mice demonstrated much higher bacterial loads in their lungs and an increased dissemination of the infection. The acute phase reaction attenuated lung inflammation during pneumonia, as reflected by histopathology, reduced pulmonary levels of proinflammatory cytokines, and a strongly diminished recruitment of neutrophils to the site of infection. Blood neutrophils harvested from turpentine injected mice displayed a reduced capacity to up-regulate their CD11b/CD18 expression upon stimulation with Pseudomonas ex vivo and during Pseudomonas pneumonia in vivo. Administration of a blocking anti-CD11b antibody to turpentine-injected and control mice almost completely abrogated the difference in bacterial outgrowth, whereas inhibition of the sympathetic nervous system did not affect the impaired pulmonary host defense in mice with an acute phase response. CONCLUSIONS: These data suggest that a systemic acute phase response might impair host defense against P. aeruginosa pneumonia, possibly in part by inhibition of CD11b/CD18-dependent neutrophil recruitment
U2 - https://doi.org/10.1097/01.CCM.0B013E3181620652
DO - https://doi.org/10.1097/01.CCM.0B013E3181620652
M3 - Article
C2 - 18091542
SN - 0090-3493
VL - 36
SP - 580
EP - 587
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 2
ER -