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A Randomized, controlled trial of Acyclovir prophylaxis versus placebo among HIV/HSV-2 co-infected individuals (through the Rakai Health Sciences Program)


Interventions that slow HIV-1 disease progression among persons with CD4+ counts above 250 cells/µL could postpone the need for antiretroviral therapy (ART) and prolong life-expectancy for HIV-infected persons. Herpes simplex virus type 2 (HSV-2) has been shown to up-regulate HIV-1 replication at the cellular level.(1) This finding has been supported by clinical evidence that individuals who are HSV-2 seropositive at the time of HIV-1 seroconversion had higher HIV viral loads at 5 and 15 months post-seroconversion.(2) Earlier studies during the era of zidovudine (Retrovir®) monotherapy showed a survival advantage when acyclovir (ACV, Zovirax®) was added to the treatment of patients with HIV.(3) Acyclovir prophylaxis has been shown to decrease herpes simplex virus infections and varicella-zoster virus infections among HIV infected patients in a meta-analysis of randomized trials from North America and Europe. This analysis also found a reduced risk of mortality among patients treated with acyclovir. The potential of acyclovir to slow HIV-1 disease progression has not been assessed in a randomized trial in Africa where high rates of HSV-2 infection have been observed among HIV-1 infected individuals. This study proposes to assess the benefits of acyclovir prophylaxis among HIV-1 infected individuals dually infected with HSV-2 who are not on ART through a randomized double-blind placebo controlled trial.


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