TY - JOUR
T1 - Aspiration pneumonitis primes the host for an exaggerated inflammatory response during pneumonia
AU - van Westerloo, David J.
AU - Knapp, Sylvia
AU - van't Veer, Cornelis
AU - Buurman, Wim A.
AU - de Vos, Alex F.
AU - Florquin, Sandrine
AU - van der Poll, Tom
PY - 2005
Y1 - 2005
N2 - Objective. Nosocomial pneumonia is a feared complication in the critically ill patient. Aspiration pneumonitis is frequently complicated by infections. The objective of this study was to determine the influence of aspiration pneumonitis on the host response to a common nosocomial respiratory pathogen. Design. Controlled, in vivo laboratory study. Setting. Research laboratory of a health sciences university. Subjects. Female C57BI/6 mice. Interventions: Mice received hydrochloric acid or saline intratracheally followed 16 hrs later by Klebsiella pneumoniae. Measurements and Main Results. Hydrochloric acid induced a mild aspiration pneumonitis. Nonetheless, hydrochloric acid aspiration resulted in a markedly increased inflammatory response in the lung on infection with K. pneumoniae. This enhanced inflammatory reaction was accompanied by a greatly increased outgrowth of K. pneumoniae in lungs of mice previously exposed to hydrochloric acid. Preexisting aspiration pneumonitis also triggered mouse lungs in vivo and alveolar macrophages ex vivo for enhanced release of proinflammatory mediators on stimulation with Klebsiella lipopolysaccharide. Inhibition of tumor necrosis factor-alpha resulted in an increased inflammatory reaction and enhanced bacterial outgrowth in mice with primary X pneumoniae pneumonia, whereas it had no effect in mice with preexisting aspiration pneumonitis. Conclusions: These data indicate a) that aspiration pneumonitis renders the host more susceptible to respiratory tract infection with K. pneumoniae, concurrently priming the lung for an exaggerated inflammatory response; and b) that although tumor necrosis factor-alpha plays a major role in the host response to primary infection, it does not affect lung inflammation or defense after aspiration pneumonitis
AB - Objective. Nosocomial pneumonia is a feared complication in the critically ill patient. Aspiration pneumonitis is frequently complicated by infections. The objective of this study was to determine the influence of aspiration pneumonitis on the host response to a common nosocomial respiratory pathogen. Design. Controlled, in vivo laboratory study. Setting. Research laboratory of a health sciences university. Subjects. Female C57BI/6 mice. Interventions: Mice received hydrochloric acid or saline intratracheally followed 16 hrs later by Klebsiella pneumoniae. Measurements and Main Results. Hydrochloric acid induced a mild aspiration pneumonitis. Nonetheless, hydrochloric acid aspiration resulted in a markedly increased inflammatory response in the lung on infection with K. pneumoniae. This enhanced inflammatory reaction was accompanied by a greatly increased outgrowth of K. pneumoniae in lungs of mice previously exposed to hydrochloric acid. Preexisting aspiration pneumonitis also triggered mouse lungs in vivo and alveolar macrophages ex vivo for enhanced release of proinflammatory mediators on stimulation with Klebsiella lipopolysaccharide. Inhibition of tumor necrosis factor-alpha resulted in an increased inflammatory reaction and enhanced bacterial outgrowth in mice with primary X pneumoniae pneumonia, whereas it had no effect in mice with preexisting aspiration pneumonitis. Conclusions: These data indicate a) that aspiration pneumonitis renders the host more susceptible to respiratory tract infection with K. pneumoniae, concurrently priming the lung for an exaggerated inflammatory response; and b) that although tumor necrosis factor-alpha plays a major role in the host response to primary infection, it does not affect lung inflammation or defense after aspiration pneumonitis
U2 - https://doi.org/10.1097/01.CCM.0000172277.41033.F0
DO - https://doi.org/10.1097/01.CCM.0000172277.41033.F0
M3 - Article
C2 - 16096455
SN - 0090-3493
VL - 33
SP - 1770
EP - 1778
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 8
ER -