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Infection and Immunity, August 2000, p. 4811-4814, Vol. 68, No. 8
Department of Microbiology and Infectious
Diseases,1 Department of Medical
Sciences,2 and Department of
Internal Medicine,3 University of Calgary,
Calgary, Alberta T2N 4N1, Canada
Received 6 March 2000/Returned for modification 20 April
2000/Accepted 15 May 2000
Pseudomonas aeruginosa infection of cystic fibrosis
patients causes lung damage that is substantially orchestrated by
cytokines. In this study, multi-gene probe analysis was used to
characterize the ability of the P. aeruginosa
mitogen, exoenzyme S, to induce proinflammatory and
immunoregulatory cytokines and chemokines. Exoenzyme S strongly induced
transcription of proinflammatory cytokines and chemokines (tumor
necrosis factor alpha, interleukin-1
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Pseudomonas aeruginosa Exoenzyme S
Induces Transcriptional Expression of Proinflammatory Cytokines
and Chemokines
[IL-1
], IL-1
, IL-6,
IL-8, MIP-1
, MIP-1
, MCP-1, RANTES, and I-309), modest
transcription of immunoregulatory cytokines (IL-10 and IL-12p40), and
weak transcription of Th1 cytokines (IL-2 and gamma interferon).
The response occurred early and subsided without evolving over time.
These data suggest that cells responding to exoenzyme S
would rapidly express proinflammatory cytokines and chemokines that may contribute to pulmonary inflammation in
cystic fibrosis.
*
Corresponding author. Mailing address: Heritage Medical
Research Building, Rm. 273, 3330 Hospital Dr., N.W., University of Calgary, Calgary, Alberta, Canada T2N-4N1. Phone: (403) 220-8479. Fax:
(403) 270-2772. E-mail: cmody{at}ucalgary.ca.
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