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    Acyclovir and transmission of HIV-1 from persons infected with HIV-1 and HSV-2.

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    Date
    2010
    Author
    Celum C, Lingappa JR, Magaret AS Wald A,
    Wang RS, Mujugira A, Baeten JM Mugo N,
    Mullins JI, Bukusi EA, Cohen CR Hughes JP,
    Katabira E, Kiarie J, Farquhar C Ronald A,
    Stewart GJ, Essex M, Were E Makhema J,
    Fife KH, Gray GE, McIntyre JA de Bruyn G,
    Manongi R, Coetzee D, Allen S Kapiga S,
    Inambao M, Karita E, Kanweka W Kayitenkore K,
    Delany S, Vwalika B, Stevens W Rees H,
    Campbell MS, Coombs RW, Morrow R Thomas KK,
    Whittington WL, Barnes L, Ridzon R, McElrath MJ,
    Corey, L
    Type
    Article
    Language
    en
    Metadata
    Show full item record

    Abstract
    ACKGROUND: Most persons who are infected with human immunodeficiency virus type 1 (HIV-1) are also infected with herpes simplex virus type 2 (HSV-2), which is frequently reactivated and is associated with increased plasma and genital levels of HIV-1. Therapy to suppress HSV-2 reduces the frequency of reactivation of HSV-2 as well as HIV-1 levels, suggesting that suppression of HSV-2 may reduce the risk of transmission of HIV-1. METHODS: We conducted a randomized, placebo-controlled trial of suppressive therapy for HSV-2 (acyclovir at a dose of 400 mg orally twice daily) in couples in which only one of the partners was seropositive for HIV-1 (CD4 count, > or = 250 cells per cubic millimeter) and that partner was also infected with HSV-2 and was not taking antiretroviral therapy at the time of enrollment. The primary end point was transmission of HIV-1 to the partner who was not initially infected with HIV-1; linkage of transmissions was assessed by means of genetic sequencing of viruses. RESULTS: A total of 3408 couples were enrolled at 14 sites in Africa. Of the partners who were infected with HIV-1, 68% were women, and the baseline median CD4 count was 462 cells per cubic millimeter. Of 132 HIV-1 seroconversions that occurred after randomization (an incidence of 2.7 per 100 person-years), 84 were linked within couples by viral sequencing: 41 in the acyclovir group and 43 in the placebo group (hazard ratio with acyclovir, 0.92, 95% confidence interval [CI], 0.60 to 1.41; P=0.69). Suppression with acyclovir reduced the mean plasma concentration of HIV-1 by 0.25 log(10) copies per milliliter (95% CI, 0.22 to 0.29; P<0.001) and the occurrence of HSV-2-positive genital ulcers by 73% (risk ratio, 0.27; 95% CI, 0.20 to 0.36; P<0.001). A total of 92% of the partners infected with HIV-1 and 84% of the partners not infected with HIV-1 remained in the study for 24 months. The level of adherence to the dispensed study drug was 96%. No serious adverse events related to acyclovir were observed. CONCLUSIONS: Daily acyclovir therapy did not reduce the risk of transmission of HIV-1, despite a reduction in plasma HIV-1 RNA of 0.25 log(10) copies per milliliter and a 73% reduction in the occurrence of genital ulcers due to HSV-2. (ClinicalTrials.gov number, NCT00194519.) 2010 Massachusetts Medical Society
    URI
    http://www.ncbi.nlm.nih.gov/pubmed/20089951
    http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/32477
    Citation
    N Engl J Med. 2010 Feb 4;362(5):427-39. doi: 10.1056/NEJMoa0904849. Epub 2010 Jan 20.
    Publisher
    Department of Global Health, University of Washington, Harborview Medical Center, 325 Ninth Ave.
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    • Faculty of Arts & Social Sciences (FoA&SS / FoL / FBM) [6727]

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