Departments of Microbiology,1 Biochemistry and Molecular Pharmacology,4 Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania,5 Tulane National Primate Research Center, Covington, Louisiana,2 Department of Surgery, Duke University, Durham, North Carolina3
Received 19 May 2004/ Accepted 4 August 2004
Rabies virus (RV) has recently been developed as a novel vaccine candidate for human immunodeficiency virus type 1 (HIV-1). The RV glycoprotein (G) can be functionally replaced by HIV-1 envelope glycoprotein (Env) if the gp160 cytoplasmic domain (CD) of HIV-1 Env is replaced by that of RV G. Here, we describe a pilot study of the in vivo replication and immunogenicity of an RV with a deletion of G (
G) expressing a simian/human immunodeficiency virus SHIV89.6P Env ectodomain and transmembrane domain fused to the RV G CD (
G-89.6P-RVG) in a rhesus macaque. An animal vaccinated with
G-89.6P-RVG developed SHIV89.6P virus-neutralizing antibodies and SHIV89.6P-specific cellular immune responses after challenge with SHIV89.6P. There was no evidence of CD4+ T-cell loss, and plasma viremia was controlled to undetectable levels by 6 weeks postchallenge and has remained suppressed out to 22 weeks postchallenge.
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