The ability to recognize HIV antigens is lost early in HIV-1 infection
. Individuals with nonprogressive HIV disease have been observed to mo
unt strong immune responses against the virus and have become a paradi
gm to emulate with immune-based therapies. Highly active antiviral dru
g therapy (HAART) has now become the standard of care for HIV-l-infect
ed individuals. Because HIV-specific anergy occurs early in HIV infect
ion, HAART initiated after primary infection may not reconstitute HIV-
specific immune function. We have been investigating the effects of an
immune-based therapy, called REMUNE, in HIV-l-seropositive individual
s. REMUNE has been observed to stimulate HIV-1-specific immune functio
n measured by delayed-type hypersensitivity, lymphocyte proliferation,
Th1 cytokine, and beta-chemokine production. Multiple Phase II studie
s and a Phase III clinical end-point study are ongoing in thousands of
seropositive individuals in order to test the clinical utility of REM
UNE. The clinical testing of REMUNE and other promising immune-based t
herapies may provide additional treatment modalities useful in the chr
onic management of HIV-1.