Zhao X X, Liao M J, Rashidbaigi A
Interferon Sciences Inc, New Brunswick, NJ 08901-3605, USA.
Cytokines Cell Mol Ther. 1998 Mar;4(1):11-6.
Treatment of human peripheral blood leukocytes (hPBL) with Sendai virus induces significant production of human interferon-alpha (IFN-alpha). Addition of human recombinant interleukin-10 (IL-10) to hPBL in vitro prior to treatment with Sendai virus resulted in considerable inhibition of IFN-alpha production. Downregulation of IFN-alpha production was IL-10 concentration-dependent and observed at IL-10 concentrations of as low as 0.05 ng/ml, with a median effective dose (ED50) of about 5 ng/ml. Inhibition of IFN-alpha production by IL-10 occurred at an early stage of Sendai virus induction. The inhibitory effect of IL-10 on leukocyte interferon production was specific and blocked by pretreatment with neutralizing polyclonal anti-IL-10 antibody. This downregulatory effect is at the transcriptional level, since IL-10 inhibits IFN-alpha mRNA accumulation upon Sendai virus treatment. These data suggest that leukocyte IFN-alpha production is a highly regulated process that is modulated by cytokines such as IL-10 during early immunological response to infection.
用仙台病毒处理人外周血白细胞(hPBL)可诱导大量产生人α干扰素(IFN-α)。在用仙台病毒处理之前,于体外向hPBL中添加人重组白细胞介素-10(IL-10),可导致IFN-α产生受到显著抑制。IFN-α产生的下调呈IL-10浓度依赖性,在低至0.05 ng/ml的IL-10浓度下即可观察到,中位有效剂量(ED50)约为5 ng/ml。IL-10对IFN-α产生的抑制发生在仙台病毒诱导的早期阶段。IL-10对白细胞干扰素产生的抑制作用具有特异性,可被用中和性多克隆抗IL-10抗体预处理所阻断。这种下调作用发生在转录水平,因为IL-10在仙台病毒处理后可抑制IFN-α mRNA的积累。这些数据表明,白细胞IFN-α的产生是一个高度受调控的过程,在对感染的早期免疫反应中受到诸如IL-10等细胞因子的调节。