Removal of herpes simplex virus (HSV) -infected cells from peripheral
sites such as the skin is mainly an activity of T cells, particularly
the CD4(+) T subset, Such cells orchestrate an inflammatory response w
ith interferon-gamma (IFN-gamma) appearing to play the essential role
in viral clearance, In accordance with this hypothesis, we show that i
nfection of BALB/c background mice expressing the knockout phenotype f
or IFN-gamma (GKO mice) are significantly more susceptible to the deve
lopment of cutaneous zosteriform lesions than are wild-type, However,
following HSV immunization, GKO mice become solidly immune to the deve
lopment of zosteriform lesions, in addition, the transfer of T cells f
rom immune GKO mice to nude mice recipients renders them resistant to
zosteriform lesions. Our results are discussed in terms of the major a
nd compensatory mechanisms available to the body to effect immunity to
viral infections.