摘要
A proposed scheme between the possibleinteractions of pro- and anti-inflammatory cytokines,NO and G-CSF during severe inflammation/infection ispresented. Taken together, these data indicate that G-CSF exhibits anti-inflammatory properties which mayprove to be beneficial in situations associated with anincreased activity of the cellular immune system.Since the suppressive effects of G-CSF on theproduction of pro-inflammatory mediators like "FNF-αand nitric oxide are most likely neither cell type
A proposed scheme between the possible interactions of pro- and anti-inflammatory cytokines, NO and G-CSF during severe inflammation/infection is presented. Taken together, these data indicate mat G-CSF exhibits anti-inflammatory properties which may prove to be beneficial in situations associated with an increased activity of the cellular immune system. Since the suppressive effects of G-CSF on the production of pro-inflammatory mediators like TNF-α and nitric oxide are most likely neither cell type nor tissue specific, it is conceivable that NO release induced by pro-inflammatory mediators can be reduced by G-CSF in various organ systems and in different forms of shock. In this context, G-CSF might represent a counterregulatory mechanism directed against a downstream oriented inflammatory response to infection. Therefore, the investigation of G-CSF in the prophylaxis of nonneutropenic infections, sepsis, and other severe inflammatory disorders seems reasonable.
出处
《中国药理学报》
CSCD
1999年第8期673-681,共9页
Acta Pharmacologica Sinica
基金
Project supported in part by AMGEN GesmbH,Vienna,Austria. GH is supported by a grant from the BONFOR-Kommission (160/11).
关键词
细胞因子类
感染
脓毒症
一氧化氮合酶
G-CSF
granulocyte colony-stimulating factor
cytokines
infection
inflammation
sepsis
nitric-oxide synthase