Containment of the acquired immunodeficiency syndrome (AIDS) epidemic
will require an effective human immunodeficiency virus type 1 (HIV-1)
vaccine. Accumulating evidence suggests that such a vaccine must effic
iently elicit an HIV-1-specific cytotoxic T lymphocyte (CTL) response.
Nonhuman primate models will continue to provide an important tool fo
r assessing the extent of protective immunity induced by various immun
ization strategies. Although replication-competent AIDS viruses attenu
ated for pathogenicity by selective gene deletions have provided prote
ctive immunity in nonhuman primate models, the long-term safety of-suc
h vaccines in human populations is suspect. Inactivated virus and subu
nit vaccines have elicited neither CTLs nor antibodies capable of neut
ralizing a wide array of patient HIV-1 isolates. Considerable effort i
s now being focused on evaluating live vector-based vaccine and plasmi
d DNA vaccine approaches for preventing HIV-1 infection both in animal
model and human studies. Our growing understanding of the biology of
HIV-1 and immune responses to this virus will continue to suggest impr
oved vaccination approaches for exploration.