Risk Factors for HSV-2 Infection among Sexual Partners of HSV-2/HIV-1 Co-Infected Persons
© Mujugira et al; licensee BioMed Central Ltd. 2011
Received: 1 March 2011
Accepted: 15 March 2011
Published: 15 March 2011
Herpes simplex virus type 2 (HSV-2) is the most frequent cause of genital ulcer disease worldwide and has been associated with increased risk for HIV-1 acquisition and transmission. We conducted a cross-sectional analysis of risk factors for HSV-2 infection among HIV-1 uninfected partners, whose partners were co-infected with HIV-1 and HSV-2.
Between November 2004 and April 2007, 3408 HIV-discordant couples, in which the HIV-1 infected partners were HSV-2 seropositive with CD4 250 cells/mm3 or greater, were enrolled in an HSV-2 suppression trial to prevent HIV-1 transmission at 14 sites in 7 African countries. Clinical & behavioral data, HSV-2 and HIV-1 testing were conducted at enrolment. Univariate and multivariate Poisson regression analyses were performed separately, by gender of the HIV-1 infected partner.
Among 3354 HIV-1 uninfected participants, 32% were female and overall 71% were HSV-2 seropositive. Among couples with female HIV-1 infected partners, HIV-1 plasma RNA [aPR 1.03; 95% CI: 0.99 to 1.06; p = 0.11] and CD4 count [aPR 1.00; 95% CI: 0.98 to 1.01; p = 0.48] in the HSV-2/HIV-1 dually infected female and circumcision in the HIV-1 uninfected male partner [aPR 0.94; 95% CI: 0.88 to 1.00; p = 0.06] were not associated with reduced risk of HSV-2 seropositivity, after adjusting for other factors.
In this cross-sectional analysis of African HIV-1 serodiscordant heterosexual couples with prevalent HSV-2 infection in the HIV-1 infected partner, HIV-1 plasma RNA and CD4 count in the dually-infected partner and male circumcision in the HIV-1 uninfected partner were not associated with HSV-2 concordance.
Herpes simplex virus type 2 (HSV-2) is the most common cause of genital ulcer disease (GUD) worldwide. HSV-2 prevalence in sub-Saharan Africa ranges from 27-57% in men to 30-74% in women [1, 2] and is higher in HIV-1 infected persons . Epidemiologic studies suggest synergy between HIV-1 and HSV-2 that facilitates the spread of both viruses, with HSV-2 increasing HIV-1 susceptibility and infectiousness  and HIV-1 infection increasing HSV-2 reactivation frequency .
The increased risk of HIV-1 transmission and acquisition due to HSV-2 infection in the context of an overall high risk of HIV-1 transmission among stable, heterosexual HIV-1 serodiscordant couples (one partner HIV-1 infected and the other HIV-1 uninfected) , which are highly prevalent in Africa , make evaluation of risk factors for HSV-2 within HIV-1 serodiscordant couples from diverse parts of Africa of interest.
We conducted a cross-sectional analysis of risk factors for HSV-2 seropositivity in >3300 HIV-1 uninfected members of African HIV-1 serodiscordant couples in which the HIV-1 infected partner was dually-infected with HSV-2. In particular, we sought to assess whether HIV-1 plasma RNA level or CD4 count in the HIV-1 infected partner, as indicators of higher HIV-1 infectiousness and more advanced immunosuppression, modifies HSV-2 infectiousness, and if male circumcision in the HIV-uninfected partners of women with HSV-2/HIV-1 dual infection protected them from HSV-2 acquisition.
From November 2004 to April 2007, 3408 heterosexual HIV-1 discordant couples from 14 sites in Botswana, Kenya, Rwanda, South Africa, Tanzania, Uganda and Zambia were enrolled into the Partners in Prevention HSV/HIV Transmission Study, a randomized clinical trial of suppressive acyclovir therapy to reduce sexual HIV-1 transmission from HSV-2/HIV-1 dually-infected women and men to their HIV-1 uninfected partners . HIV-1 discordant couples were eligible for enrolment into the trial if they were sexually active and planning to remain partnered for at least 24 months and if the HIV-1-infected participant was HSV-2 infected, had a CD4 count 250 cells/mm3 or greater, was not on antiretroviral therapy, and was not pregnant. HIV-1 uninfected members of the discordant couples could be either HSV-2 seropositive or seronegative. Clinical and behavioral data collected at study enrolment were used for this analysis.
HIV-1 testing was done using 2 rapid assays in parallel, most commonly Determine HIV-1/2 (Abbott Diagnostics), Uni-Gold HIV-1 (Trinity Biotech), or Capillus HIV-1/HIV-2 (Trinity Biotech) and paired positive rapid assay results were confirmed by HIV-1 EIA . At all study sites, HSV-2 serostatus was determined using HerpeSelect HSV-2 gG2-based EIA (Focus Technologies). Given the results of previous studies using this assay in African cohorts, a cut-off value of ≥3.5 was chosen to define seropositivity, in order to improve test specificity [8–10]. CD4 quantification was performed for HIV-1 infected participants at 6-month intervals using standard flow cytometry. Plasma HIV-1 RNA was quantified using the COBAS Ampliprep/COBAS TaqMan real-time HIV-1 RNA assay, version 1.0 (Roche Diagnostics, Indianapolis, IN). All HIV-1 and HSV-2 serologic results were confirmed by Western blot, performed at the University of Washington .
Data were entered onto standard case report forms and faxed to a central database at the University of Washington. Analysis was done using SAS version 9.1 (SAS Institute, Cary, NC). Univariate and multivariate analyses were performed using Poisson regression with HSV-2 status of the partner participant as the outcome variable. In order to examine male circumcision and to allow for other possible gender differences in transmission risk, separate analyses were performed for male and female HIV-1 infected participants. Backward elimination, starting with all variables significant at p < 0.1 in univariate regression, was performed to select a final multivariate model.
Institutional review boards at the University of Washington and at all collaborating site organizations approved study procedures. All participants provided written informed consent. The trial was registered through ClinicalTrials.gov (NCT00194519).
Characteristics of study population
Of 3408 enrolled HIV-1-uninfected participants, 3354 were eligible for this analysis (54 were excluded because either they or their partner were ineligible for the study, based on confirmatory HIV-1 or HSV-2 testing). HIV-1 seronegative partners had a median age of 35 years and 1084 (32%) were female. Couples reported a median of 4 sex acts in the month prior to enrollment (IQR 2-8). The seroprevalence of HSV-2 among HIV-1 seronegative partners was 71% overall; 63% in men versus 89% in women (p < 0.001). By study design, all HIV-1 infected partners were co-infected with HSV-2. Median CD4 count among HIV-1 infected partners was 462 cells/mm3 (IQR 347-631) and median plasma HIV-1 RNA was 4.1 log10 copies/mL (IQR 3.3-4.7).
Risk factors for HSV-2 infection among HIV-1 uninfected partners
Population characteristics and risk factors for HSV-2 seropositivity among HIV-1 uninfected members of African HIV-1 serodiscordant partnerships
HIV-1 uninfected female partners of males dually-infected with HSV-2 and HIV-1 (N = 1084)
HIV-1 uninfected male partners of females dually-infected with HSV-2 and HIV-1 (N = 2270)
(n = 123)
# (%) or median (IQR)
(n = 961)
# (%) or median (IQR)
(n = 841)
# (%) or median (IQR)
(n = 1429)
# (%) or median (IQR)
Characteristics of HIV-1/HSV-2
Genital lesions at enrollment
Plasma HIV-1 RNA
Has any other sexual partners
Characteristics of HIV-1 uninfected
Years of education
Has any other sexual partners
Male partner is circumcised (physical exam)
Female partner uses hormonal contraceptives
Female uses vaginal drying
Couple characteristics ‡
Couple is married
Duration of sexual relationship
Years living together
Number of children
Number of sex acts with study part-ner in previous month (median, IQR)
Any sex acts with partner in previous month
Any unprotected sex with study partner in previous month
Enrollment site in Eastern (vs. southern) Africa
Among female HIV-1 uninfected partners of HIV-1/HSV-2 dually-infected males, only older age (aPR 1.08, p < 0.0001) and greater number of years of education (aPR 0.90, p = 0.001) of the HIV-1 infected partner were associated with HSV-2 seropositivity.
Notably, neither HIV-1 plasma RNA level [aPR 1.03; 95% CI: 0.99 to 1.06; p = 0.11] nor CD4 count [aPR 1.00; 95% CI: 0.98 to 1.01; p = 0.48], factors that might indicate increased HSV-2 infectiousness , were associated with increased risk of HSV-2 infection in HIV-1 uninfected partners.
In this multi-national study of 3354 African HIV-1 serodiscordant couples in which one partner was dually-infected with HIV-1 and HSV-2, HIV-1 plasma RNA and CD4 count of the HIV-1 infected partner were not significantly associated with HSV-2 infection concordance in the HIV-1 uninfected partner. Furthermore, despite a recent prospective clinical trial reporting association of male circumcision with reduced HSV-2 acquisition , male circumcision in male HIV-1 uninfected partner was only marginally protective against HSV-2 infection in our cross-sectional multivariate analysis.
Prevalence of HSV-2 in the HIV-1 uninfected partner was high in our study (63% in men and 89% in women) compared to other African cohorts [14, 15], possibly due to the high rate of HSV-2 transmission reported in stable, long-term partnerships [16, 17]. Also consistent with other studies [18–20], HSV-2 infection at enrollment in the HIV-1 uninfected partner was significantly associated with older age and was higher among women compared to men. The former may indicate that age is a surrogate for duration of sexual exposure in these couples .
A limitation of this cross-sectional study was the inability to determine temporal relationships of HIV-1 and HSV-2 infection in the dually-infected partner or recency of HSV-2 infection in the HIV-uninfected partners, thus limiting our analysis of behavioral correlates with HSV-2 infection. HSV-2 concordance may reflect HSV-2 transmission within the couple or acquisition outside the partnership. Our study eligibility criteria included that couples be sexually active and intend to remain together; as such we may have selected for older, more stable couples.
In summary, among African HIV-1 serodiscordant couples in which all the HIV-infected partners were dually infected with HSV-2, 71% of their HIV-1 uninfected partners had HSV-2 infection, and HSV-2 infection in the HIV-uninfected partner was not associated with HIV-1 plasma RNA and CD4 count in the HIV-infected partner, or male circumcision in the HIV-1 uninfected partner. Given the need to identify interventions to reduce HSV-2 transmission, future research should focus on prospective analysis of risk factors for HSV-2 transmission, which will be conducted in this cohort.
We are grateful to the study participants for their participation and dedication. We thank the study team members at the research sites and at the University of Washington for their contributions to study implementation and data collection. This study was supported through a research grant from the Bill & Melinda Gates Foundation (grant ID # 26469)
Partners in Prevention HSV/HIV Transmission Study Team:
University of Washington Coordinating Center and Central Laboratories, Seattle, USA: Connie Celum (principal investigator), Anna Wald (protocol co-chair), Jairam Lingappa (medical director), Jared M. Baeten, Mary Campbell, Lawrence Corey, Robert W. Coombs, James P. Hughes, Amalia Magaret, M. Juliana McElrath, Rhoda Morrow, James I. Mullins
Study sites and site principal investigators:
Cape Town, South Africa (University of Cape Town): David Coetzee; Eldoret, Kenya (Moi University, Indiana University): Kenneth Fife, Edwin Were; Gaborone, Botswana (Botswana Harvard Partnership): Max Essex, Joseph Makhema; Kampala, Uganda (Infectious Disease Institute, Makerere University): Elly Katabira, Allan Ronald; Kigali, Rwanda (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, Kayitesi Kayitenkore, Etienne Karita; Kisumu, Kenya (Kenya Medical Research Institute, University of California San Francisco): Elizabeth Bukusi, Craig Cohen; Kitwe, Zambia (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, William Kanweka; Lusaka, Zambia (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, Bellington Vwalika; Moshi, Tanzania (Kilimanjaro Christian Medical College, Harvard University): Saidi Kapiga, Rachel Manongi; Nairobi, Kenya (University of Nairobi, University of Washington): Carey Farquhar, Grace John-Stewart, James Kiarie; Ndola, Zambia (Rwanda Zambia HIV Research Group, and Emory University): Susan Allen, Mubiana Inambao; Orange Farm, South Africa (Reproductive Health Research Unit, University of the Witwatersrand): Sinead Delany-Moretlwe, Helen Rees; Soweto, South Africa (Perinatal HIV Research Unit, University of the Witwatersrand): Guy de Bruyn, Glenda Gray, James McIntyre; Thika, Kenya (University of Nairobi, University of Washington): Nelly Rwamba Mugo
Data management was provided by DF/Net Research, Inc. (Seattle, USA) and site laboratory oversight was provided by Contract Lab Services (University of the Witwatersrand, Johannesburg, South Africa).
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