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

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dc.contributor.author Celum, Connie
dc.contributor.author Were, Edwin
dc.contributor.author Fife, Kenneth H.
dc.contributor.author Bruyn, Guy de
dc.contributor.author Gray, Glenda E.
dc.contributor.author McIntyre, James A.
dc.contributor.author Manongi, Rachel
dc.contributor.author Kapiga, Saidi
dc.contributor.author Coetzee, David
dc.contributor.author Allen, Susan
dc.contributor.author Inambao, Mubiana
dc.contributor.author Kayitenkore, Kayitesi
dc.contributor.author Karita, Etienne
dc.contributor.author Kanweka, William
dc.date.accessioned 2021-07-12T07:33:02Z
dc.date.available 2021-07-12T07:33:02Z
dc.date.issued 2010
dc.identifier.uri https://doi.org/10.1056/NEJMoa0904849
dc.identifier.uri http://ir.mu.ac.ke:8080/jspui/handle/123456789/4822
dc.description.abstract Background 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, ≥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 log10 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 log10 copies per milliliter and a 73% reduction in the occurrence of genital ulcers due to HSV-2. (ClinicalTrials.gov number, NCT00194519. opens in new tab.) en_US
dc.language.iso en en_US
dc.publisher Massachusetts Medical Society en_US
dc.subject HIV-1 transmission en_US
dc.subject HSV-2 infection en_US
dc.title Acyclovir and transmission of HIV-1 from persons infected with HIV-1 and HSV-2 en_US
dc.type Article en_US


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