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Differential cytokine production in stimulated blood cultures from intensive care patients with bacterial infections
Authors:Dr. I. G. Mitov  Dr. A. Kropec  Dr. A. Benzing  Dr. H. Just  Dr. G. Garotta  Dr. C. Galanos  PD Dr. med. M. Freudenberg
Affiliation:(1) Max-Planck-Institut für Immunbiologie, Stübeweg 51, D-79108 Freiburg;(2) Krankenhaushygiene, Hugstetter Str. 55, D-79106 Freiburg, Germany;(3) Anaesthesiologie, Hugstetter Str. 55, D-79106 Freiburg, Germany;(4) Innere Medizin III, Universitätsklinikum, Hugstetter Str. 55, D-79106 Freiburg, Germany;(5) Hoffmann-La Roche, Zentrale Forschungseinheit, Basel, Switzerland;(6) Max-Planck-Institut für Immunbiologie, Stübeweg 51, D-79108 Freiburg, Germany
Abstract:Summary Mice infected with bacteria develop an interferon-gamma (IFN-gamma) dependent hypersensitivity to lipopolysaccharide (LPS) and other bacterial components. The broader aim of this study is to find out whether such hypersensitivity also occurs in patients suffering from bacterial infections. The capacity of stimulated peripheral blood cells from infected, intensive-care patients to produce cytokines (IFN-gamma, tumor necrosis factor-alpha (TNF-agr) and interleukin-6 (IL-6)) was compared to that of healthy donors. Culturing of the cells was carried out preferentially in whole blood diluted 1:3. Whole blood cultures (WBC) were stimulated with lipopolysaccharide (LPS), whole killedSalmonella typhimurium andStaphylococcus aureus and concanavalin A (ConA), and the cytokine production was determined. Two main findings emerged from this study: The IFN-gamma production by WBC of patients was, compared to healthy donors, markedly suppressed, regardless of stimulus used. Further, patients' WBC exhibited a suppressed TNF-agr production after stimulation with LPS. Surprisingly, following stimulation with bacteria (S. typhimurium andS. aureus) an elevated TNF-agr and IL-6 response was obtained. Thus, in severely infected patients the cytokine responses of peripheral blood cells to LPS may be suppressed, while the response to other bacterial components is enhanced.
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