Abstract
BackgroundIn HIV-infected children, viral diversity tends to increase with age in the absence of antiretroviral treatment (ART). We measured HIV diversity in African children (ages 6–36 months) enrolled in a randomized clinical trial comparing two ART regimens (Cohort I of the P1060 trial). Children in this cohort were exposed to single dose nevirapine (sdNVP) at birth.MethodsHIV diversity was measured retrospectively using a high resolution melting (HRM) diversity assay. Samples were obtained from 139 children at the enrollment visit prior to ART initiation. Six regions of the HIV genome were analyzed: two in gag, one in pol, and three in env. A single numeric HRM score that reflects HIV diversity was generated for each region; composite HRM scores were also calculated (mean and median for all six regions).ResultsIn multivariable median regression models using backwards selection that started with demographic and clinical variables, older age was associated with higher HRM scores (higher HIV diversity) in pol (P = 0.005) and with higher mean (P = 0.014) and median (P<0.001) HRM scores. In multivariable models adjusted for age, pre-treatment HIV viral load, pre-treatment CD4%, and randomized treatment regimen, higher HRM scores in pol were associated with shorter time to virologic suppression (P = 0.016) and longer time to study endpoints (virologic failure [VF], VF/death, and VF/off study treatment; P<0.001 for all measures).ConclusionsIn this cohort of sdNVP-exposed, ART-naïve African children, higher levels of HIV diversity in the HIV pol region prior to ART initiation were associated with better treatment outcomes.
Highlights
Mother-to-child transmission (MTCT) of HIV can occur in utero, at the time of delivery, or during breastfeeding [1]
We developed an assay based on high resolution melting (HRM) technology that can be used to quantify the genetic diversity of HIV populations without sequencing [17]
In a previous study of 31 HIV-infected infants in Uganda, we found that higher HRM scores in the gag and pol regions were associated with older age and decreased 5-year survival [4]
Summary
Mother-to-child transmission (MTCT) of HIV can occur in utero, at the time of delivery, or during breastfeeding [1]. Most HIV-infected infants have relatively homogeneous viral populations that tend to diversify over time [2,3,4,5]. Most studies of HIV diversity have used methods based on the comparison of sequences from individual HIV variants, which is time consuming and costly This often limits the number of individuals, samples, and genomic regions that can be analyzed. We measured HIV diversity in African children (ages 6–36 months) enrolled in a randomized clinical trial comparing two ART regimens (Cohort I of the P1060 trial). Children in this cohort were exposed to single dose nevirapine (sdNVP) at birth
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