Frese Michael, Barth Kerstin, Kaul Artur, Lohmann Volker, Schwärzle Verena, Bartenschlager Ralf
Abteilung Molekulare Virologie, Hygiene Institut, Universität Heidelberg, Otto-Meyerhof-Zentrum, Im Neuenheimer Feld 350, D-69120 Heidelberg, Germany.
Abteilung Virologie, Institut für Medizinische Mikrobiologie und Hygiene, Universität Freiburg, Hermann-Herder-Str. 11, D-79104 Freiburg, Germany.
J Gen Virol. 2003 May;84(Pt 5):1253-1259. doi: 10.1099/vir.0.18997-0.
It was demonstrated using self-replicating hepatitis C virus (HCV) RNAs that both types of interferons (IFNs) (in particular IFN-alpha and IFN-gamma) are potent inhibitors of HCV replication in Huh-7 cells. Because IFN-gamma and tumour necrosis factor (TNF)-alpha trigger a partially overlapping set of antiviral defence mechanisms, it is tempting to speculate that TNF-alpha also inhibits HCV replication. However, this study shows that TNF-alpha does not affect HCV protein and RNA synthesis, nor does it synergistically enhance the inhibitory effect of IFN-gamma. Taken together, these results demonstrate that HCV replication in Huh-7 cells is highly resistant to TNF-alpha. It is, therefore, unlikely that the increased production of TNF-alpha, which is seen in many hepatitis C patients, contributes to HCV clearance by inducing antiviral defence mechanisms in infected hepatocytes.
使用自我复制的丙型肝炎病毒(HCV)RNA证明,两种类型的干扰素(IFN)(特别是IFN-α和IFN-γ)是Huh-7细胞中HCV复制的有效抑制剂。由于IFN-γ和肿瘤坏死因子(TNF)-α触发了一组部分重叠的抗病毒防御机制,因此很容易推测TNF-α也抑制HCV复制。然而,这项研究表明,TNF-α不影响HCV蛋白质和RNA合成,也不会协同增强IFN-γ的抑制作用。综上所述,这些结果表明Huh-7细胞中的HCV复制对TNF-α具有高度抗性。因此,在许多丙型肝炎患者中观察到的TNF-α产量增加不太可能通过诱导受感染肝细胞中的抗病毒防御机制来促进HCV清除。