Interferon (IFN) therapy of chronic hepatitis C has proved useful in r
ecent years. A major goal in the treatment of hepatitis C is the preve
ntion of the high relapse rate after cessation of therapy and the impr
ovement of the response rate in non-responders. Several approaches can
be tried. The administration of higher doses of IFN results in an inc
rease in the response rate, but does not prevent ultimate relapse. Sim
ilarly, prolongation of the treatment period gives better results, but
one third of cases still relapse. In these cases, re-treatment result
s in ALT normalization once again, but does not prevent subsequent rel
apse; in non-responders to IFN, re-treatment will not lead to improvem
ent of the response rate. Analysis of the viral genome reveals its pre
sence in serum in spite of the normalization of ALT values. The role o
f HCV genome heterogeneity in the response to IFN needs to be assessed
and it is necessary to find other antiviral agents that are able to c
lear HCV from all relevant hosts (serum, liver tissue and mononuclear
cells).