TY - JOUR
T1 - Secreted Interferon-Inducible Factors Restrict Hepatitis B and C Virus Entry in Vitro
AU - Xia, Yuchen
AU - Cheng, Xiaoming
AU - Blossey, Christoph K.
AU - Wisskirchen, Karin
AU - Esser, Knud
AU - Protzer, Ulrike
N1 - Publisher Copyright:
© 2017 Yuchen Xia et al.
PY - 2017
Y1 - 2017
N2 - Interferon-α (IFN-α) 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-α-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-α is able to induce soluble factors that can bind to heparan glycosaminoglycans thus leading to the inhibition of viral binding.
AB - Interferon-α (IFN-α) 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-α-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-α is able to induce soluble factors that can bind to heparan glycosaminoglycans thus leading to the inhibition of viral binding.
UR - http://www.scopus.com/inward/record.url?scp=85015955903&partnerID=8YFLogxK
U2 - 10.1155/2017/4828936
DO - 10.1155/2017/4828936
M3 - Article
C2 - 28367455
AN - SCOPUS:85015955903
SN - 2314-8861
VL - 2017
JO - Journal of Immunology Research
JF - Journal of Immunology Research
M1 - 4828936
ER -