Hepatitis C virus (HCV) infection is one of the more important infecti
ous diseases yet to be conquered. An estimated 3.5 million people in t
he USA have chronic HCV. Each year, 8000 to 10000 of these chronically
infected patients die of a liver-related complication of their infect
ion. The introduction of effective blood screening assays has resulted
in a remarkable decrease in the incidence of post-transfusion HCV inf
ection. Nonetheless it is essential to have a treatment programme for
chronic HCV disease that prevents the development and the progression
of compensated cirrhosis to either decompensated cirrhosis or hepatoce
llular carcinoma, as many individuals present to the health care syste
m with chronic active hepatitis or cirrhosis, A completely safe and ef
fective treatment strategy for chronic HCV, with or without cirrhosis,
remains to be developed. Of the various treatment alternatives curren
tly available, only interferon (IFN) has been evaluated extensively. I
FN therapy has been shown to induce remissions of the hepatic inflamma
tory process and also to eliminate the viral infection in some treated
cases. As a result, the selection of patients for treatment and the d
ose and the duration of therapy with IFN are still controversial issue
s. It is widely held that cirrhotic individuals do not respond to IFN
therapy and that treatment of decompensated cirrhotic individuals with
HCV infection is dangerous. Here we review data regarding the availab
le experience with IFN treatment of HCV-positive individuals with cirr
hosis and compare the response rates of cirrhotics to those reported f
or individuals with chronic active HCV.