Hepatitis C virus RNA replication is resistant to tumour necrosis factor-α

被引:70
作者
Frese, M
Barth, K
Kaul, A
Lohmann, V
Schwärzle, V
Bartenschlager, R
机构
[1] Univ Freiburg, Inst Med Mikrobiol & Hyg, Abt Virol, D-79104 Freiburg, Germany
[2] Heidelberg Univ, Otto Meyerhof Zentrum, Inst Hyg, Abt Mol Virol, D-69120 Heidelberg, Germany
关键词
D O I
10.1099/vir.0.18997-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:1253 / 1259
页数:7
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