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α干扰素和利巴韦林对成熟树突状细胞功能的影响。

Impact of alpha interferon and ribavirin on the function of maturing dendritic cells.

作者信息

Barnes Eleanor, Salio Mariolina, Cerundolo Vincenzo, Medlin Joanne, Murphy Shona, Dusheiko Geoffrey, Klenerman Paul

机构信息

Nuffield Department of Medicine, University of Oxford, Oxford OX1 3SY, UK.

出版信息

Antimicrob Agents Chemother. 2004 Sep;48(9):3382-9. doi: 10.1128/AAC.48.9.3382-3389.2004.

Abstract

Alpha interferon and ribavirin are required in combination to achieve a sustained virological response in the treatment of hepatitis C virus (HCV) infection. Alpha interferon has direct antiviral activity and also enhances HCV-specific T-cell responses. Ribavirin has little direct activity against HCV but reduces hepatic inflammation. It is therefore likely that these drugs in combination have hitherto unidentified immunological effects. In the present study we investigated the effects of alpha interferon and ribavirin on dendritic cell (DC) maturation and cytokine production induced by double-stranded RNA in vitro. Alpha interferon alone enhanced the expression of HLA class I, HLA class II, and CD86 on immature DCs but did not stimulate full DC maturation, which requires the expression of CD83. Alpha interferon enhanced the production of interleukin 12 p70 [IL-12(p70)] and tumor necrosis factor alpha (TNF-alpha) but had no effect on IL-10 production. In contrast, ribavirin at physiological doses had no effect on DC maturation but markedly suppressed the production of TNF-alpha, IL-10, and IL-12(p70). The suppression of cytokines by ribavirin cannot be explained by the induction of DC apoptosis or cell death. Quantitative PCR confirmed that cytokine suppression occurs at the level of mRNA. The suppression of IL-12(p70) and TNF-alpha in maturing DCs may explain the reduction in hepatic inflammation observed during ribavirin monotherapy. Combination alpha interferon-ribavirin therapy may alter the cytokine profile of maturing DCs overall by suppressing IL-10 production but maintaining IL-12(p70) and TNF-alpha production, a pattern that would favor viral elimination through downstream effects on T cells.

摘要

在丙型肝炎病毒(HCV)感染的治疗中,需要联合使用α干扰素和利巴韦林才能实现持续的病毒学应答。α干扰素具有直接抗病毒活性,还能增强HCV特异性T细胞应答。利巴韦林对HCV几乎没有直接活性,但可减轻肝脏炎症。因此,这两种药物联合使用可能具有迄今尚未明确的免疫效应。在本研究中,我们在体外研究了α干扰素和利巴韦林对双链RNA诱导的树突状细胞(DC)成熟和细胞因子产生的影响。单独使用α干扰素可增强未成熟DC上HLA I类、HLA II类和CD86的表达,但不会刺激DC完全成熟,而DC完全成熟需要CD83的表达。α干扰素可增强白细胞介素12 p70 [IL-12(p70)]和肿瘤坏死因子α(TNF-α)的产生,但对IL-10的产生没有影响。相比之下,生理剂量的利巴韦林对DC成熟没有影响,但可显著抑制TNF-α、IL-10和IL-12(p70)的产生。利巴韦林对细胞因子的抑制作用不能用诱导DC凋亡或细胞死亡来解释。定量PCR证实细胞因子抑制发生在mRNA水平。成熟DC中IL-12(p70)和TNF-α的抑制可能解释了利巴韦林单药治疗期间观察到的肝脏炎症减轻。联合使用α干扰素和利巴韦林治疗可能通过抑制IL-10的产生但维持IL-12(p70)和TNF-α的产生,总体上改变成熟DC的细胞因子谱,这种模式有利于通过对T细胞的下游作用消除病毒。

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