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Clinical and Diagnostic Laboratory Immunology, 11 1995, 689-692, Vol 2, No. 6
AM van Furth, EM Seijmonsbergen, JA Langermans, PH van der Meide and R van Furth
The present study concerns the release of the proinflammatory cytokines
interleukin-1 beta (IL-1 beta) and tumor necrosis factor alpha and of the
anti-inflammatory cytokine IL-10 by human leukocytes in whole blood during
stimulation with Streptococcus pneumoniae and the effects of various
xanthine derivates, i.e., pentoxifylline (PTX), caffeine, and theofylline,
and of dexamethasone (DXM). All three xanthine derivates and DXM inhibited
the release of tumor necrosis factor alpha, PTX being the most effective.
PTX, theofylline, and DXM inhibited the release of IL-1 beta, but caffeine
did not affect IL-1 beta release. The release of IL-10 was significantly
reduced by PTX at 24 h and by caffeine at 48 h, but DXM increased the
release of this cytokine. In sum, the results of this study demonstrate
that DXM inhibits only the release of proinflammatory cytokines but not of
the anti-inflammatory cytokine IL- 10 by human leukocytes, while PTX is the
most potent inhibitor of both proinflammatory and anti-inflammatory
cytokines.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Effect of xanthine derivates and dexamethasone on Streptococcus pneumoniae-stimulated production of tumor necrosis factor alpha, interleukin-1 beta (IL-1 beta), and IL-10 by human leukocytes
Department of Infectious Diseases, University Hospital, Leiden, The Netherlands.
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