Key Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai, China.
Nat Immunol. 2013 Aug;14(8):793-803. doi: 10.1038/ni.2647. Epub 2013 Jul 7.
The cell-to-cell transmission of viral resistance is a potential mechanism for amplifying the interferon-induced antiviral response. In this study, we report that interferon-α (IFN-α) induced the transfer of resistance to hepatitis B virus (HBV) from nonpermissive liver nonparenchymal cells (LNPCs) to permissive hepatocytes via exosomes. Exosomes from IFN-α-treated LNPCs were rich in molecules with antiviral activity. Moreover, exosomes from LNPCs were internalized by hepatocytes, which mediated the intercellular transfer of antiviral molecules. Finally, we found that exosomes also contributed to the antiviral response of IFN-α to mouse hepatitis virus A59 and adenovirus in mice. Thus, we propose an antiviral mechanism of IFN-α activity that involves the induction and intercellular transfer of antiviral molecules via exosomes.
病毒耐药性的细胞间传播是放大干扰素诱导的抗病毒反应的潜在机制。在这项研究中,我们报告称,干扰素-α(IFN-α)诱导了耐药性从非允许的肝非实质细胞(肝非实质细胞)到允许的肝细胞的传递,这是通过外泌体实现的。IFN-α 处理的肝非实质细胞来源的外泌体富含具有抗病毒活性的分子。此外,肝非实质细胞来源的外泌体被肝细胞内化,介导了抗病毒分子的细胞间转移。最后,我们发现外泌体也有助于 IFN-α 对小鼠肝炎病毒 A59 和腺病毒在小鼠中的抗病毒反应。因此,我们提出了一种 IFN-α 活性的抗病毒机制,该机制涉及通过外泌体诱导和细胞间转移抗病毒分子。