Journal
JOURNAL OF VIROLOGY
Volume 76, Issue 7, Pages 3570-3574Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.76.7.3570-3574.2002
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Funding
- NCI NIH HHS [R01 CA040489, R37 CA040489, CA40489] Funding Source: Medline
- NIAID NIH HHS [AI49665, F32 AI049665] Funding Source: Medline
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Hepatitis B virus (HBV) replication is inhibited in a noncytopathic manner by alpha/beta interferon (IFN-alpha/beta) and IFN-gamma. We demonstrate here that inhibitors of cellular proteasome activity can block this antiviral effect. These results suggest that a critical component of the IFN-induced antiviral response may be the proteasome-dependent degradation of viral or cellular proteins that are required for HBV replication.
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