Human herpesvirus 7, reported in 1990 is a lymphotropic member of the betah
erpesvirus subfamily of herpesviruses. The virus is highly seroprevalent, p
rimary infection usually occurs during childhood, and it has been associate
d with cases of exanthem subitum, pityriasis rosea, neurological manifestat
ions and transplant complications. The latter two may warrant antiviral int
ervention, in vitro studies have shown that HHV-7 is susceptible to several
nucleoside phosphonate compounds. In vitro, the virus has approximately a
5 day growth cycle in cultured lymphocytes; in vivo, latency is established
in peripheral blood T-cells and a persistent infection is established in s
alivary gland tissue from which infectious virus is constitutively shed in
saliva. The HHV-7 genome is approximately 145 kb and encodes at least 84 di
fferent proteins. Studies characterising HHV-7 gene products and the requir
ed interactions between viral and cellular genes necessary for virus replic
ation, persistence and latency are in their infancy. HHV-7 infection has a
variety of effects on host cells including upregulation of interleukin 15 a
nd down-modulation of the cell surface molecule CD4; the latter serves as t
he cellular membrane receptor for HHV-7. Since HIV also infects T-cells via
the CD4 molecule, the interactions of these viruses within T-cells during
the course of AIDS are important areas of investigation.