Hepatitis C virus (HCV) infection is a leading cause of chronic hepatitis,
liver cirrhosis, and hepatocellular carcinoma worldwide, Therapeutic option
s for hepatitis C are limited. Standard monotherapy with interferon-alpha l
eads to a sustained response in only 10-20% of patients, Recent studies hav
e shown improved sustained response rates for the combination of interferon
-a and ribavirin. Despite these improvements, more effective therapies are
needed, A variety of alternative agents are currently being evaluated in cl
inical trials, Recent advances in the molecular virology of hepatitis C hav
e identified specific antiviral targets such as the viral NS3 serine protea
se, the RNA helicase, and the RNA-dependent RNA polymerase, In addition, ge
ne therapeutic strategies aimed at inhibiting HCV gene expression and repli
cation as well as immunotherapeutic concepts aimed at enhancing the cellula
r immune response against HCV are being explored in various experimental sy
stems. These and other novel antiviral strategies may complement the existi
ng therapeutic modalities in the future.