Mestan J, Brockhaus M, Kirchner H, Jacobsen H
Institute of Virus Research, German Cancer Research Center, Heidelberg, F.R.G.
J Gen Virol. 1988 Dec;69 ( Pt 12):3113-20. doi: 10.1099/0022-1317-69-12-3113.
Tumour necrosis factor (TNF) induces antiviral activity in HEp-2 cells. Virus yield reduction assays with vesicular stomatitis virus as challenging virus demonstrated that the antiviral state was more pronounced in confluent cultures under low serum conditions. A significant enhancement of the antiviral state was obtained by combining TNF with low concentrations of either interferon (IFN)-beta 1 or IFN-gamma. The reduction in virus yield was significantly higher than that expected from summation of the independent antiviral activities of either substance alone, i.e. TNF and IFN acted synergistically as antiviral agents. Synergism of TNF with IFN-beta or IFN-gamma appeared to be mediated by different pathways, since different requirements for pretreatment and different effects on oligo-2',5'-adenylate synthetase (2-5AS) induction were observed. Induction of 2-5AS by TNF could be shown to be an indirect event that was sensitive to an antiserum against natural IFN-beta 1.
肿瘤坏死因子(TNF)可诱导HEp-2细胞产生抗病毒活性。以水疱性口炎病毒作为攻击病毒进行病毒产量减少试验表明,在低血清条件下的汇合培养物中,抗病毒状态更为明显。通过将TNF与低浓度的干扰素(IFN)-β1或IFN-γ联合使用,可显著增强抗病毒状态。病毒产量的降低显著高于单独使用任何一种物质(即TNF和IFN)的独立抗病毒活性之和所预期的水平,也就是说,TNF和IFN作为抗病毒剂具有协同作用。TNF与IFN-β或IFN-γ的协同作用似乎是由不同途径介导的,因为观察到预处理的要求不同,对寡聚2',5'-腺苷酸合成酶(2-5AS)诱导的影响也不同。TNF对2-5AS的诱导可被证明是一个间接事件,对天然IFN-β1的抗血清敏感。