Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/4822
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCelum, Connie-
dc.contributor.authorWere, Edwin-
dc.contributor.authorFife, Kenneth H.-
dc.contributor.authorBruyn, Guy de-
dc.contributor.authorGray, Glenda E.-
dc.contributor.authorMcIntyre, James A.-
dc.contributor.authorManongi, Rachel-
dc.contributor.authorKapiga, Saidi-
dc.contributor.authorCoetzee, David-
dc.contributor.authorAllen, Susan-
dc.contributor.authorInambao, Mubiana-
dc.contributor.authorKayitenkore, Kayitesi-
dc.contributor.authorKarita, Etienne-
dc.contributor.authorKanweka, William-
dc.date.accessioned2021-07-12T07:33:02Z-
dc.date.available2021-07-12T07:33:02Z-
dc.date.issued2010-
dc.identifier.urihttps://doi.org/10.1056/NEJMoa0904849-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/4822-
dc.description.abstractBackground 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.isoenen_US
dc.publisherMassachusetts Medical Societyen_US
dc.subjectHIV-1 transmissionen_US
dc.subjectHSV-2 infectionen_US
dc.titleAcyclovir and transmission of HIV-1 from persons infected with HIV-1 and HSV-2en_US
dc.typeArticleen_US
Appears in Collections:School of Medicine

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.