Heterologous prime/boost regimens have the potential for raising high Level
s of immune responses. Here we report that DNA priming followed by a recomb
inant modified vaccinia Ankara (rMVA) booster controlled a highly pathogeni
c immunodeficiency virus challenge in a rhesus macaque model. Both the DNA
and rMVA components of the vaccine expressed multiple immunodeficiency viru
s proteins. Two DNA inoculations at 0 and 8 weeks and a single rMVA booster
at 24 weeks effectively controlled an intrarectal challenge administered 7
months after the booster. These findings provide hope that a relatively si
mple multiprotein DNA/MVA vaccine can help to control the acquired immune d
eficiency syndrome epidemic.