The discovery of hepatitis C virus (HCV) in 1987 and the subsequent de
velopment of diagnostic tests has accounted for the majority of cases
of viral hepatitis throughout the world. However, a significant number
of cases cannot be assigned to any of the viral hepatitis groups (A -
E). During 1995 two companies reported the identification of novel he
patitis viruses known as GBV-B and hepatitis G virus (HGV), which were
found to be responsible for a large proportion of the remaining undia
gnosed cases. Sequence analysis of these two viruses revealed them to
be isolates of the same virus and, moreover, to be close homologues of
HCV. The clinical significance of these new viruses is currently uncl
ear, but preliminary epidemiologic evidence suggests they are often fo
und as co-infections with HCV. The close similarity of these viruses t
o HCV and the fact that related viruses have also been identified whic
h infect small primates, suggests that they may be useful as surrogate
agents for the identification of novel therapeutic agents against HCV
. Current therapeutic agents against HCV are still disappointing altho
ugh more encouraging data have been reported on long-term combination
therapy with interferon-ce and ribavirin. Studies have continued aimed
towards developing assays for biochemical functions specified by vira
l proteins and these are still mainly focused on the multi-functional
NS3 protein.