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Antimicrobial Agents and Chemotherapy, September 1999, p. 2291-2294, Vol. 43, No. 9
Centre de Recherche en Infectiologie, Centre
Hospitalier de l'Université Laval, and Département de
Microbiologie, Faculté de Médecine, Université Laval,
Sainte-Foy, Québec, Canada G1V 4G2
Received 22 February 1999/Returned for modification 16 April
1999/Accepted 23 June 1999
Encapsulated Klebsiella pneumoniae strains
frequently induce fatal nosocomial pneumonia. Cefodizime (CEF) as
an antibiotic is suspected to enhance host resistance against various
microbial invasions through interactions with bacteria and host cells.
To investigate the influence of CEF on the pulmonary response to Klebsiella that does not merely result from direct
bacterial clearance by the drug, we inoculated mice with heat-killed
fluorescein isothiocyanate-labeled K. pneumoniae. CEF
upregulated (P < 0.01) the early
Klebsiella-induced secretion of tumor necrosis factor
alpha, as well as the number (P < 0.01) and
phagocytic efficacy (P < 0.001) of alveolar
macrophages. By contrast, the late polymorphonuclear neutrophil
recruitment (P < 0.05) and levels of interleukin-1
alpha (IL-1
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Influence of Cefodizime on Pulmonary Inflammatory
Response to Heat-Killed Klebsiella pneumoniae in
Mice
) (P < 0.05) and IL-6
(P < 0.05) were reduced. The stimulation of an early immune response by CEF followed by late reduction in inflammation may
be beneficial against bacterial pneumonia.
*
Corresponding author. Mailing address: Centre de
Recherche en Infectiologie, Centre Hospitalier de l'Université
Laval, 2705 Boul. Laurier, Sainte-Foy, Québec, Canada G1V 4G2.
Phone: (418) 654-2705. Fax: (418) 654-2715. E-mail:
michel.g.bergeron{at}crchul.ulaval.ca.
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