van Furth A M, Steenwijk T M, Langermans J A, van Furth R
Department of Infectious Diseases, University Hospital, Leiden, The Netherlands.
Pediatr Res. 1994 Jun;35(6):725-8. doi: 10.1203/00006450-199406000-00020.
The effects of dexamethasone, pentoxifylline, and MAb against endotoxin (HA-1A) on the release of various proinflammatory mediators, i.e. tumor necrosis factor-alpha (TNF), IL-1 beta, IL-8, and prostaglandin 2, by human leukocytes during stimulation with Haemophilus influenzae type B were studied. The results show that only monocytes, and thus neither lymphocytes nor granulocytes, release these mediators in response to H. influenzae. Dexamethasone inhibited the release of all of these mediators, whereas pentoxifylline only inhibited the release of TNF. HA-1A only reduced the release of IL-8 from adherent monocytes significantly and had no significant effect on the release of TNF, IL-1 beta, and prostaglandin E2. In whole blood, no significant effect of HA-1A on the release of TNF, IL-1 beta, IL-8, and prostaglandin E2 was found. In summary, the results of this study demonstrate that dexamethasone is the most potent inhibitor of the release of proinflammatory mediators by monocytes induced by H. influenzae type B.
研究了地塞米松、己酮可可碱和抗内毒素单克隆抗体(HA-1A)对B型流感嗜血杆菌刺激人白细胞释放各种促炎介质(即肿瘤坏死因子-α(TNF)、白细胞介素-1β(IL-1β)、白细胞介素-8(IL-8)和前列腺素E2)的影响。结果表明,只有单核细胞,而不是淋巴细胞和粒细胞,对B型流感嗜血杆菌产生反应释放这些介质。地塞米松抑制所有这些介质的释放,而己酮可可碱仅抑制TNF的释放。HA-1A仅显著降低黏附单核细胞释放IL-8,对TNF、IL-1β和前列腺素E2的释放无显著影响。在全血中,未发现HA-1A对TNF、IL-1β、IL-8和前列腺素E2的释放有显著影响。总之,本研究结果表明,地塞米松是B型流感嗜血杆菌诱导单核细胞释放促炎介质的最有效抑制剂。