There is no vaccine for HCV and the only available treatment, IFN alpha alo
ne or in combination with ribavirin, has proven efficacious in less than 50
% of patients, Given that approximately 200 million chronic HCV infections
have been estimated worldwide, there is a pressing need to develop vaccinat
ion strategies aimed at preventing and possibly eradicating HCV infection,
However, several major practical and scientific problems arise in designing
an HCV vaccine. First, HCV is only readily detected as RNA by PCR, Second,
the only species that can be infected by HCV are humans and chimpanzees. T
hird, the virus does not replicate efficiently in vitro, Fourth, some viral
proteins have very high mutability, Last, there is little information on c
orrelates of immunity. Although an ideal vaccine should protect from infect
ion, in that it should elicit sterilizing immunity, this is quite an ambiti
ous goal in the PCR era. In the case of HCV: where acute HCV infection is a
very Limited health problem and infection can only be assessed by PCR, a m
ore realistic goal might be to look for vaccines capable of protecting from
chronic infection. We have preliminary evidence in chimpanzees that an HCV
vaccine consisting of recombinant envelope proteins can elicit antibodies
and inflammatory CD4+ T cell responses which can prevent chronic infection
in the majority of vaccinees, Although the scientific and clinical challeng
es that need to be addressed are still substantial, advances in recombinant
protein technology, novel adjuvants, and DNA vaccines, will be key in deve
loping strategies to generate protective immunity against chronic HCV infec
tion.