Institute of Virology, Technische Universität München/Helmholtz Zentrum München, 81675 Munich, Germany.
Institute of Virology, Technische Universität München/Helmholtz Zentrum München, 81675 Munich, Germany; German Center for Infection Research (DZIF), Partner Site Munich, Munich, Germany.
J Immunol Res. 2017;2017:4828936. doi: 10.1155/2017/4828936. Epub 2017 Mar 6.
Interferon- (IFN-) has been used for more than 20 years as the first-line therapy for hepatitis B virus (HBV) and hepatitis C virus (HCV) infection, because it has a number of antiviral effects. In this study, we describe a novel mode of its antiviral action. We demonstrate that the supernatant from IFN--treated cultured cells restricted HBV and HCV infection by inhibiting viral entry into hepatoma cells. The factors contained in the supernatant competed with the virus for binding to heparan glycosaminoglycans-the nonspecific attachment step shared by HBV and HCV. Secreted factors of high molecular mass that bind to heparin columns elicited the antiviral effect. In conclusion, IFN- is able to induce soluble factors that can bind to heparan glycosaminoglycans thus leading to the inhibition of viral binding.
干扰素- (IFN-) 已被用作乙型肝炎病毒 (HBV) 和丙型肝炎病毒 (HCV) 感染的一线治疗药物超过 20 年,因为它具有多种抗病毒作用。在这项研究中,我们描述了其抗病毒作用的一种新机制。我们证明,IFN-处理的培养细胞上清液通过抑制病毒进入肝癌细胞来限制 HBV 和 HCV 的感染。上清液中包含的因子与病毒竞争与肝素糖胺聚糖结合 - HBV 和 HCV 共有的非特异性附着步骤。与肝素柱结合的高分子质量分泌因子引发了抗病毒作用。总之,IFN- 能够诱导能够与肝素糖胺聚糖结合的可溶性因子,从而导致病毒结合的抑制。