Abstract

BackgroundEarly combination antiretroviral therapy (cART) reduces the size of the viral reservoir in paediatric and adult HIV infection. Very early-treated children may have higher cure/remission potential. MethodsIn an observational study of 151 in utero (IU)-infected infants in KwaZulu-Natal, South Africa, whose treatment adhered strictly to national guidelines, 76 infants diagnosed via point-of-care (PoC) testing initiated cART at a median of 26 h (IQR 18–38) and 75 infants diagnosed via standard-of-care (SoC) laboratory-based testing initiated cART at 10 days (IQR 8–13). We analysed mortality, time to suppression of viraemia, and maintenance of aviraemia over the first 2 years of life. FindingsBaseline plasma viral loads were low (median 8000 copies per mL), with 12% of infants having undetectable viraemia pre-cART initiation. However, barely one-third (37%) of children achieved suppression of viraemia by 6 months that was maintained to >12 months. 24% had died or were lost to follow up by 6 months. Infant mortality was 9.3%. The high-frequency virological failure in IU-infected infants was associated not with transmitted or acquired drug-resistant mutations but with cART non-adherence (plasma cART undetectable/subtherapeutic, p<0.0001) and with concurrent maternal cART failure (OR 15.0, 95%CI 5.6–39.6; p<0.0001). High-frequency virological failure was observed in PoC- and SoC-tested groups of children. InterpretationThe success of early infant testing and cART initiation strategies is severely limited by subsequent cART non-adherence in HIV-infected children. Although there are practical challenges to administering paediatric cART formulations, these are overcome by mothers who themselves are cART-adherent. These findings point to the ongoing obligation to address the unmet needs of the mothers. Eliminating the particular barriers preventing adequate treatment for these vulnerable women and infants need to be prioritised in order to achieve durable suppression of viraemia on cART, let alone HIV cure/remission, in HIV-infected children. FundingWellcome Trust, National Institutes of Health.

Highlights

  • Initiation of combination antiretroviral therapy early in HIV infection reduces the size of the viral reservoir, estimated by the frequency of HIV DNA in peripheral blood cells, both in paediatric and adult infection [1À3]

  • To further explore the factors, including combination antiretroviral therapy (cART) non-adherence and drug resistance, underlying success or failure of early cART in this group, we studied in utero (IU)-infected infants enroled from hospitals in KwaZulu-Natal, South Africa where the prevention of mother-to-child transmission (PMTCT) programme has been very effective

  • Two-thirds of infants (103/151, 68%) received both NVP and AZT, the remaining one-third (48/151, 32%) receiving NVP or AZT only. Of these 151 IUinfected infants, 76 were identified through PoC (n = 70) or overnight viral load (n = 6) testing of infants, and cART was initiated at a median age of 26 h (IQR 18À38)

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Summary

Introduction

Initiation of combination antiretroviral therapy (cART) early in HIV infection reduces the size of the viral reservoir, estimated by the frequency of HIV DNA in peripheral blood cells, both in paediatric and adult infection [1À3]. IU-MTCT rates have fallen from 7% to 0.5% since the provision of cART to all HIV-infected mothers during pregnancy [1,12] but HIV seroprevalence in mothers attending antenatal clinics has continued to rise even since the introduction of cART in 2004, and approaches 40% [13]. This setting provided the opportunity to evaluate the success of early cART on outcome following IU-infection

Study design and participants
Ethics
Study definitions
Procedures
Analysis and outcomes
Statistical analysis
Role of the funding source
Results
11 Child 90 12 Mother 2
Discussion
Declaration of Competing Interest
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