Recombinant, replication-competent rabies virus (RV) vaccine strain-based v
ectors were developed expressing HIV type I (HIV-1) envelope glycoprotein (
gp160) from both a laboratory-adapted (CXCR4-tropic) and a primary (dual-tr
opic) HIV-1 isolate. An additional transcription stop/start unit within the
RV genome was used to express HIV-1 gp160 in addition to the other RV prot
eins, The HIV-1 gp160 protein was stably and functionally expressed, as ind
icated by fusion of human T cell lines after infection with the recombinant
RVs, Inoculation of mice with the recombinant RVs expressing HIV-1 gp160 i
nduced a strong humoral response directed against the HIV-1 envelope protei
n after a single boost with recombinant HIV-1 gp120 protein. Moreover, high
neutralization titers up to 1:800 against HIV-1 could be detected in the m
ouse sera. These data indicate that a live recombinant RV, a rhabdovirus, e
xpressing HIV-1 gp160 may serve as an effective vector for an HIV-1 vaccine
.