Herpesviruses are a diverse family of large DNA viruses, all of which
have the capacity to establish lifelong latent infections. Many differ
ent herpesviruses may have potential as gene delivery vehicles, but ex
ploitation of this potential has, to date, been explored only using He
rpes simplex virus (HSV), a virus which naturally establishes a silent
, latent infection of neurones in man and in a number of experimental
animal models. Delivery of reporter genes in vitro and in vivo has bee
n demonstrated using a variety of replication competent and replicatio
n defective vectors, and significant physiological modification in the
CNS has been achieved by HSV-mediated gene delivery. Much remains to
be done using animal models and, in particular, the requirements for l
ong-term gene expression from latent virus genomes needs to be defined
in different cell types in vivo.