Geĭn O N, Gorshkova K G, Geĭn S V
Patol Fiziol Eksp Ter. 2010 Jan-Mar(1):10-3.
It was established that in a mononuclear fraction polyoxidonium inhibited the TNF-alpha production and stimulated the IL-1 beta and IL-6 production. In LPS-induced mononuclear cultures polyoxidonium inhibited the IL-6 production and had no statistically significant effect on the synthesis of TNF-alpha and IL-1 beta. Polyoxidonium had no effect on TNF-alpha, IL-6 and IL-1 beta production by purified monocytes. The addition of polyoxidonium with dexamethasone to the cultures only in monocyte fraction enhanced the IL-1 beta production as compared with the effect of dexamethasone alone. Data obtained allow suggesting that under certain conditions polyoxidonium could alleviate pronounced suppressive influence of glucocorticoids on a secretory activity of effectors of innate immunity.
已确定在单核细胞组分中,聚氧化膦抑制肿瘤坏死因子-α(TNF-α)的产生,并刺激白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的产生。在脂多糖(LPS)诱导的单核细胞培养物中,聚氧化膦抑制IL-6的产生,而对TNF-α和IL-1β的合成无统计学显著影响。聚氧化膦对纯化单核细胞产生TNF-α、IL-6和IL-1β没有影响。仅在单核细胞组分的培养物中,将聚氧化膦与地塞米松一起添加,与单独使用地塞米松相比,增强了IL-1β的产生。所获得的数据表明,在某些条件下,聚氧化膦可以减轻糖皮质激素对先天免疫效应器分泌活性的明显抑制作用。