The potential role of hydroxyurea in the treatment of human immunodeficienc
y virus (HIV) infection was first supported by in vitro experiments that de
monstrated control of viral production in activated and resting T cells. Mo
re recently controlled clinical trials demonstrated that the addition of hy
droxyurea to nucleoside-including regimens (chiefly of didanosine but also
of stavudine and lamivudine) enhances their antiviral potency. It is believ
ed that the cytostatic effect of hydroxyurea is at least partially responsi
ble for its antiviral effect, through the down-modulation of cellular proli
feration. Such an effect has also been credited for the blunted CD4 T cell
responses that are characteristically observed when hydroxyurea is added to
nucleoside-including regimens. The adjunctive antiviral effect of hydroxyu
rea-as well as its favorable dosing schedule, safety profile, and cost-make
s it a. very attractive addition to our therapeutic armamentarium. Further
research is urgently needed to delineate the most appropriate use of this c
ompound in the setting of HIV antiretroviral therapy.