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
Am. Vanfurth et al., 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, Clinical and diagnostic laboratory immunology, 2(6), 1995, pp. 689-692
The present study concerns the release of the proinflammatory cytokine
s interleukin 1 beta (IL-1 beta) and tumor necrosis factor alpha and o
f the anti-inflammatory cytokine IL-10 by human leukocytes in whole bl
ood during stimulation with Streptococcus pneumoniae and the effects o
f various xanthine derivates, i.e., pentoxifylline (PTX), caffeine, an
d theofylline, and of dexamethasone (DXM). All three xanthine derivate
s and DXM inhibited the release of tumor necrosis factor alpha, PTX be
ing the most effective. PTX, theofylline, and DXM inhibited the releas
e of IL-1 beta, but caffeine did not affect IL-1 beta release. The rel
ease 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 o
f proinflammatory cytokines but not of the anti-inflammatory cytokine
IL-10 by human leukocytes, while PTX is the most potent inhibitor of b
oth proinflammatory and anti-inflammatory cytokines.