Virological response and resistance among HIV-infected children receiving long-term antiretroviral therapy without virological monitoring in Uganda and Zimbabwe: Observational analyses within the randomised ARROW trial

In an analysis based on the ARROW trial, Alex Szubert and colleagues report on virological and drug resistance outcomes in children with HIV infection.

Published in the journal: . PLoS Med 14(11): e32767. doi:10.1371/journal.pmed.1002432
Category: Research Article
doi: 10.1371/journal.pmed.1002432


In an analysis based on the ARROW trial, Alex Szubert and colleagues report on virological and drug resistance outcomes in children with HIV infection.


The Joint United Nations Programme on HIV/AIDS (UNAIDS) has set an ambitious target for 2020: that 90% of people living with HIV know their status, 90% of those diagnosed receive antiretroviral therapy (ART), and 90% receiving ART have viral load (VL) suppression [1]. There are an estimated 1.8 million HIV-infected children worldwide, >80% of whom live in sub-Saharan Africa. Treating children is challenging, given their more limited access to antiretroviral drugs compared with adults; in 2015, only 49% of HIV-infected children globally were estimated to be receiving ART [2]. Current WHO guidelines recommend VL monitoring 6 and 12 months after initiating ART, and every 12 months thereafter [3]. A threshold of >1,000 copies/ml is used to define virological failure, which, if confirmed and adherence has been addressed, should be followed by the switch to second-line ART. Current guidelines also recommend stopping routine CD4 monitoring, provided patients are clinically stable and virologically suppressed. However, despite this push to increase VL monitoring and reduce reliance on immunological and clinical failure criteria, the availability of VL monitoring remains limited in low-income settings (estimated at 25% of people living with HIV in 2014 [4]), and VL is less frequently measured in low-income settings than in well-resourced ones (typically annually versus 3-monthly). Therefore, it is important to understand virological outcomes among children who are not managed using real-time VL monitoring, as this reflects the reality in most ART programmes in resource-limited settings.

Although management without VL monitoring has enabled ART rollout, children with virological failure risk developing resistance, which may reduce efficacy of second-line therapy. In a systematic review of 30 studies from low-income settings in 2011 [5], 80% and 88% of children failing first-line ART had 1 or more International AIDS Society (IAS)-USA major nucleoside reverse transcriptase inhibitor (NRTI) and non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance-associated mutations, respectively. In 2012, WHO reported that 60% and 67% of adults and children in sub-Saharan Africa failing first-line ART at 12 months had NRTI and NNRTI resistance, respectively [6]. The only large randomised trial to date of second-line ART in African adults found that those receiving NRTI-based second-line regimens had equivalent virological suppression to those receiving regimens based on 2 new drug classes [7], suggesting that NRTI cross-resistance may have less relevance than feared. However, longitudinal VL and resistance data are rare in children starting first-line ART in resource-limited settings.

We therefore investigated virological outcomes and resistance in the ARROW randomised trial (ISRCTN24791884), which compared first-line ART regimens and CD4 monitoring strategies in children and adolescents in Uganda and Zimbabwe [8]. Overall, ARROW showed that CD4 monitoring, compared with clinical monitoring alone, provided some clinical benefit after the first year on ART, but 5-year survival was very high overall (96%), supporting prioritisation of ART rollout over access to laboratory monitoring. There was no evidence of differences between 3NRTI and 2NRTI+NNRTI long-term maintenance regimens in terms of clinical outcomes or CD4, but medium-term virological suppression was poorer with 3NRTI, supporting 2NRTI+NNRTI becoming the WHO-recommended first-line regimen for children as of 2013.

The ARROW trial provided a unique opportunity to evaluate long-term virological outcomes in stored samples from a large cohort of well-characterised children with high retention in whom VL monitoring was not undertaken in real-time. In the present study, we had 2 main objectives. The first was to directly compare children randomised to monitoring with and without CD4 counts in terms of long-term VL suppression and resistance. The second was to characterise the patterns of long-term virological control and resistance in children receiving first-line ART in sub-Saharan Africa without frequent, regular real-time VL monitoring (reflecting the reality in most ART programmes) in an observational analysis without regard to the trial randomisations. We focussed on children receiving currently WHO-recommended 2NRTI+NNRTI maintenance ART regimens.

Materials and methods

The ARROW trial (ISRCTN24791884) recruited 1,206 previously untreated HIV-infected children and adolescents (aged 3 months to 17 years) eligible for ART using WHO 2006 criteria [8], between 15 March 2007 and 18 November 2008. Children were recruited from 3 centres in Uganda and 1 in Zimbabwe. Caregivers gave written informed consent for all children to enrol; if older children (8–17 years) were aware of their HIV status, they gave additional assent or consent following national guidelines. The ARROW trial and this current study were approved by Research Ethics Committees and Institutional Review Boards for Uganda (Joint Clinical Research Centre and Baylor College of Medicine and the Uganda National Council for Science and Technology [UNCST]), for Zimbabwe (Medical Research Council of Zimbabwe [MRCZ/A/1321]), and for the United Kingdom (University College London [0701/001]).

Children were randomised 1:1 to clinically driven monitoring (CDM; CD4 counts measured 12-weekly in real time but not returned to physicians) or laboratory plus clinical monitoring (LCM; CD4 counts measured 12-weekly) (CONSORT diagram in Figure 1 of [8]). Children were also randomised 1:1:1 in a factorial design to 3 first-line regimens: open-label lamivudine+abacavir+NNRTI continuously (Arm-A); induction-maintenance with 4-drug lamivudine+abacavir+NNRTI+zidovudine for 36 weeks, followed by lamivudine+abacavir+NNRTI (Arm-B); or lamivudine+abacavir+zidovudine (Arm-C; 3NRTI including long-term zidovudine). The NNRTI (nevirapine/efavirenz) was chosen by clinicians according to local availability (varying by country) and child’s age. After ≥36 weeks, eligible children taking lamivudine+abacavir twice daily were randomised to continue twice daily or move to once daily [9]. Following WHO guidelines at the time [10], switch to second-line ritonavir-boosted protease-inhibitor-containing ART was discouraged in the first year of therapy. Thereafter, switch was based on clinical criteria in all participants (new/recurrent WHO stage 4 event [9]; or WHO stage 3 event(s) at clinician discretion, particularly if recurrent or persistent) or on additional immunological criteria for LCM (confirmed on-ART CD4 <15% if aged 1–2 years, <10% if aged 3–4 years, <100 cells/μL if aged ≥5 years). VLs were not measured in real time nor used for any management. Children were followed until death or planned trial closure on 16 March 2012.

Study design

In the current study, we evaluated VL and resistance in 2 separate analyses (Fig 1). First, we undertook a cross-sectional analysis (“cross-sectional study”) of VL assayed in all children on cryopreserved plasma taken up to 6 months prior to the latest of trial closure (16 March 2012) or death and also at switch to second-line; samples with VL >1,000 copies/ml were genotyped. Second, we undertook a longitudinal study in a subgroup of 316 children randomised from 29 May 2008 (“longitudinal cohort”). In these children, retrospective VL was assayed longitudinally at weeks 4, 24, 36, and 48 post-ART initiation, then every 24 weeks, with a small number of additional VLs included from a previous analysis [10] (see S1 Appendix for assay completeness over time). Genotyping was undertaken on samples with VL >1,000 copies/ml at week 48 or 144. For both studies, we present results for children taking WHO-recommended 2NRTI+NNRTI regimens in the main text and results for all children, including those randomised to 3NRTI, in S1 Appendix. The sample size for the first study was determined by the size of the trial [8] and for the second study by the size of the longitudinal cohort that aimed to include all children randomised from 29 May 2008 when seed funding was obtained.

Flow diagram of children included in virological analyses.
Fig. 1. Flow diagram of children included in virological analyses.
* Results presented in main text. ** Results presented in S1 Appendix. † 97% of children enrolled after 29 May 2008. Abbreviations: ART, antiretroviral therapy; NNRTI, non-nucleoside reverse transcriptase inhibitor; NRTI, nucleoside reverse transcriptase inhibitor; VL, viral load.

Laboratory methods

VLs were assayed blind to randomised group using Abbott m2000sp/rt or Roche COBAS Amplicor Monitor ultrasensitive tests, v1.5, with lower limit of detection of 80 copies/ml because many samples were diluted 1:2 due to low volumes. Genotyping for reverse transcriptase was done blind to randomised group using an in-house assay at a WHO-designated laboratory (Joint Clinical Research Centre, Kampala, Uganda) using the ABI 3730xl sequencer. Major NRTI and NNRTI mutations were defined using IAS-USA 2013 [11], and drug susceptibility was predicted using the Stanford algorithm version 7 [12].

Virological definitions

In the longitudinal cohort, we predefined complete VL response as <10,000 copies/ml or >1 log10 drop at week 4, <5,000 copies/ml at week 24, declining or <400 copies/ml at week 36, and subsequently <80 copies/ml at all measurements. VL measurements ≥80 copies/ml were classified as a blip if the child had a previous VL <80 copies/ml and either subsequently resuppressed <80 copies/ml (1 or 2 VL ≥80 copies/ml allowed; n = 150) or their last measurement was a single value ≥80 copies/ml (n = 31; S1 Appendix). Those not resuppressing <80 copies/ml but remaining <5,000 copies/ml were defined as persistent low-level viral load (pLLVL), whereas rebound was defined as confirmed VL ≥5,000 copies/ml (following WHO 2010 guidelines [13]). Each individual VL measurement on first-line ART was classified (S1 Table); in order to record the greatest degree of viral replication observed to have occurred, children could move from response to blip, pLLVL, and rebound states but not backwards through these states; i.e., if a child had ever experienced a VL blip, they were subsequently classified as having previously ‘blipped’.

Statistical analysis

Other than the overall comparison of VL suppression and resistance by monitoring randomisation at trial closure (protocol secondary endpoints), all analyses were exploratory and not part of the prespecified protocol (S1 Protocol) or analysis plan. Categorical factors were compared between randomised and other groups using chi-squared tests, unless otherwise stated, based on complete cases. Log10VL trajectories in pLLVL and rebound from the first measurement in the state were estimated using multilevel models with child-level random intercepts and slopes (unstructured correlation for rebound; independent for pLLVL, as correlation parameter was not estimable). Resistance was summarised at the first VL in rebound, then at the last available genotype tested subsequently, using signed-rank tests to compare repeated genotypes within each child. As VLs may be performed irregularly in clinical practice, in the longitudinal cohort we also estimated the probability that a single or confirmed VL above various thresholds (80, 200, 400, 1,000, and 5,000 copies/ml) post–week 24 would have been followed by the next VL 5–30 weeks later returning below that threshold.

All analyses were performed using Stata 14.2 (StataCorp). All P values are 2-sided.


One thousand two hundred and six children initiated ART in ARROW, aged median 6.0 years (IQR 2.4,9.3) with median CD4% 12% (7%,17%) (Table 1). Over a median 4 years follow-up, 54 children (4%) died [9], 39/54 (72%) before week 48. Sixty-seven children (6%) switched to ritonavir-boosted protease-inhibitor-containing regimens (see S1 Appendix for details of VL in children who died or switched).

Tab. 1. Characteristics at ART initiation of all children in the trial; children randomised to 2NRTI+NNRTI followed in the longitudinal cohort; and those subsequently experiencing VL blips, pLLVL, and/or rebound.
Characteristics at ART initiation of all children in the trial; children randomised to 2NRTI+NNRTI followed in the longitudinal cohort; and those subsequently experiencing VL blips, pLLVL, and/or rebound.
* Excluding 2 children who died before 4 weeks (with baseline VL only) and 2 non-responders (never achieved VL <9,500 c/ml).

Long-term virological response (cross-sectional study)

One thousand one hundred and thirty-two children (94%) were alive and in follow-up at trial closure with VL measurements available for 1,127/1,132 (99.6%) after median 3.9 years on ART (IQR 3.7,4.4). As expected, long-term virological suppression was significantly greater on the WHO-recommended 2NRTI+NNRTI maintenance regimen than 3NRTI maintenance (S1 Fig). All subsequent analyses therefore focussed on children randomised to the WHO-recommended 2NRTI+NNRTI maintenance regimen (see S1 Appendix for analyses in 3NRTI).

There was no difference in long-term virological suppression between those monitored with versus without CD4 counts (chi-squared P > 0.1 across thresholds shown in Fig 2). Among children receiving the WHO-recommended 2NRTI+NNRTI regimen, 284/378 (75%) monitored with CD4s versus 275/375 (73%) monitored without CD4s had VL <80 copies/ml after 4 years on ART (difference = +1.8% [95% CI −4.4% to +8.0%]; chi-squared P = 0.57), and 308 (81%) versus 297 (79%), respectively, had VL <1,000 copies/ml (difference = +2.3% [95% CI −3.4% to +8.0%]; chi-squared P = 0.43).

VL suppression in 2NRTI+NNRTI maintenance regimen after median 4 years on ART.
Fig. 2. VL suppression in 2NRTI+NNRTI maintenance regimen after median 4 years on ART.
Note: 95% CI for risk differences were <80 copies/ml [−4.4% to +8.0%], <200 copies/ml [−4.5% to +7.5%], <400 copies/ml [−3.6% to +8.2%], <1,000 copies/ml [−3.4% to +8.0%], <5,000 copies/ml [−1.1% to +8.7%], and <10,000 copies/ml [−0.8% to +8.4%]. Abbreviations: ART, antiretroviral therapy; CDM, clinically driven monitoring; LCM, laboratory plus clinical monitoring; NNRTI, non-nucleoside reverse transcriptase inhibitor; NRTI, nucleoside reverse transcriptase inhibitor; VL, viral load.

Of 110 children with VL >1,000 copies/ml and genotype on WHO-recommended 2NRTI+NNRTI (the vast majority on lamivudine+abacavir), only 17 (15%) had intermediate/high-level resistance to tenofovir and 10 (9%) to zidovudine, the key NRTI backbone drugs used in second-line treatment (Fig 3). There was no evidence of differences between CD4 monitoring groups in intermediate/high-level resistance to NRTIs or NNRTIs (exact P > 0.2). Prevalence of IAS-USA NRTI or NNRTI mutations was also similar (S2 Fig). 42 (82%) monitored with CD4s versus 48 (81%) without had the M184V mutation conferring resistance to lamivudine (difference = +1.0% [95% CI −13.4% to +15.4%]). Only 8 children (7%) (5 CD4-monitoring, 3 no CD4-monitoring) had the K65R NRTI mutation.

Predicted NRTI and NNRTI susceptibility in 2NRTI+NNRTI with VL &gt;1,000 copies/ml after median 4 years on ART (<i>n</i> = 110).
Fig. 3. Predicted NRTI and NNRTI susceptibility in 2NRTI+NNRTI with VL >1,000 copies/ml after median 4 years on ART (n = 110).
Note: risk differences and 95% CI between CD4 monitoring versus no CD4 monitoring with intermediate/high-level resistance were 3TC 1.0% [−13.4% to +15.4%], ABC 1.4% [−15.5% to +18.2%], ZDV 5.0% [−5.9% to +15.9%], DDI 1.1% [−16.1% to +18.3%], D4T 8.0% [−6.3% to +22.3%], FTC 1.0% [−13.4% to +15.4%], TDF 7.7% [−5.9% to +21.4%], NVP 4.7% [−14.6% to +5.2%], EFV 1.3% [−12.2% to +9.5%], ETR 0.0% [−18.1% to +18.2%], and RPV 11.6% [−28.6% to +5.5%]. Abbreviations: ART, antiretroviral therapy; CDM, clinically driven monitoring; LCM, laboratory plus clinical monitoring; NNRTI, non-nucleoside reverse transcriptase inhibitor; NRTI, nucleoside reverse transcriptase inhibitor; VL, viral load.

VL control over time on first-line WHO-recommended ART without real-time VL monitoring (longitudinal cohort)

We next evaluated virological responses over time in the 208 of the 316 longitudinal cohort children randomised to 2NRTI+NNRTI maintenance. At ART initiation, these children were broadly similar to those in the whole trial [9] (Table 1). Two children (1%) died before week 4 and had only baseline VL. Of the remaining 206 children, 204 (99%) achieved an initial VL response and were included in subsequent analyses. Only 2 children (1%) switched to second-line and 2 (1%) died after week 4 (1 VL responder, 1 in rebound).

VL measurements were classified as response, current or previous blip, pLLVL (80–5,000 copies/ml), or rebound (≥5,000 copies/ml). The differing levels of VL control over time are shown in Fig 4a. Interestingly 39 children (19%) were slow VL responders, i.e., still ≥80 copies/ml at week 36 but <80 copies/ml by week 48. After 72 weeks on ART, the percentage of children with either pLLVL or VL rebound stabilised and then remained constant; however, an increasing percentage had experienced at least 1 viral blip. In total, 93 children (46%) experienced 132 single (n = 118, 89%) or double (n = 14, 11%) blips ≥80 copies/ml, but the median (IQR) VL during these blips was only 200 (110–560) copies/ml, and children who had blipped did not progress faster to pLLVL or rebound than children remaining with complete VL response (rate 1.2 versus 4.7 per 100 child-years, respectively; S3 Fig). Overall, post–week 24, these children randomised to WHO-recommended 2NRTI+NNRTI spent 60% of child-time as complete VL responders and 85% as either complete VL responders or having had blips; 5% of time was spent with pLLVL and 10% with rebound >5,000 copies/ml. As for the cross-sectional cohort, there was no evidence of any difference in VL response between those monitored with or without CD4 counts throughout (exact P > 0.1, S3 Table).

VL response in 204 children randomised to 2NRTI+NNRTI initially responding to ART.
Fig. 4. VL response in 204 children randomised to 2NRTI+NNRTI initially responding to ART.
(a) VL classification by week on ART. (b) Mean VL during pLLVL and rebound. Note: (a) carrying forwards current state where VL was missing; carrying backwards, “VL response”, where week 4 VL was missing (n = 16). Abbreviations: ART, antiretroviral therapy; NNRTI, non-nucleoside reverse transcriptase inhibitor; NRTI, nucleoside reverse transcriptase inhibitor; pLLVL, persistent low-level viral load; VL, viral load.

Overall, 20 children (10%) experienced pLLVL. Geometric mean VL at the start of pLLVL was 780 copies/ml (95% CI 420–1,460) and did not increase over the subsequent (Kaplan-Meier) median >156 weeks (IQR 37,>156) spent with pLLVL through the end of follow-up (change −0.02 log10 per year [95% CI −0.20 to +0.16], P = 0.81; Fig 4b). In addition, some children with pLLVL resuppressed, albeit transiently; 21/105 (20%) measurements in pLLVL were <80 copies/ml.

Twenty-eight children (14%) experienced rebound to ≥5,000 copies/ml, most commonly following pLLVL (rate of progression from pLLVL to rebound 21.3/100 child-years, S3 Fig). Geometric mean VL at rebound was 41,910 copies/ml (95% CI 27,100–64,810); VL did not increase over the median of 95 weeks (IQR 25,137) spent with rebound (change −0.11 log10 per year [95% CI −0.27 to +0.05], P = 0.18; Fig 4b). In contrast to pLLVL, no measurements after confirmed rebound ≥5,000 copies/ml were <80 copies/ml.

Development of resistance on first-line 2NRTI+NNRTI without routine VL monitoring

In 12 children on 2NRTI+NNRTI with genotyping performed both at rebound and a median 2.3 (range 0.7–2.8) years subsequently, IAS-USA major NRTI mutations increased from a median (IQR) of 2 (0,2.5) to 2.5 (1.5,3.5) (median +1.0 [IQR 0.0,1.5] additional NRTI mutations per child; signed-rank P = 0.009). However, these additional NRTI mutations had little impact on predicted drug susceptibility, with only 1 child moving from no more than low-level to high-level resistance for both tenofovir and zidovudine (Fig 5). Only 5 children had repeated genotypes during pLLVL (median 2.1 [range 0.5–2.6] years between first and last genotype during pLLVL); none moved from no resistance or low-level resistance to intermediate or high-level resistance for tenofovir or zidovudine.

(a) Predicted drug susceptibility at rebound and (b) change in susceptibility over a median 2 years in those randomised to 2NRTI+NNRTI maintenance (<i>n</i> = 12).
Fig. 5. (a) Predicted drug susceptibility at rebound and (b) change in susceptibility over a median 2 years in those randomised to 2NRTI+NNRTI maintenance (n = 12).
Abbreviations: 3TC, lamivudine; ABC, abacavir; D4T, stavudine; DDI, didanosine; EFV, efavirenz; ETR, etravirine; FTC, emtricitabine; NNRTI, non-nucleoside reverse transcriptase inhibitor; NRTI, nucleoside reverse transcriptase inhibitor; NVP, nevirapine; RPV, rilpivirine; TDF, tenofovir; ZDV, zidovudine.

VL resuppression without routine VL monitoring in children randomised to 2NRTI+NNRTI maintenance

Finally, we considered the implications of the children living with low-level VLs in the context of no VL monitoring or infrequent VL measurements, as occurs in ART programmes in low-income settings. Among children in the longitudinal cohort randomised to 2NRTI+NNRTI, 36 (18%) of 203 single VL measurements ≥1,000 copies/ml were immediately followed by a subsequent VL <1,000 copies/ml. However, this depended on the level of VL: whereas 19 (40%) of 48 single VLs 1,000–4,999 copies/ml were immediately followed by a VL<1,000 copies/ml, this occurred in 17 (11%) of 155 single VLs ≥5,000 copies/ml (chi-squared P < 0.001, S4 Table). Even with confirmed VL 1,000–4,999 (i.e., 2 consecutive values ≥1,000 copies/ml with the first <5,000 copies/ml), 4/35 (11%) were immediately followed by a VL <1,000 copies/ml. In contrast, although 7/155 (5%) of single VL ≥5,000 copies/ml immediately resuppressed <80 copies/ml, no measurements after confirmed rebound ≥5,000 copies/ml were <80 copies/ml.


There are few long-term longitudinal data on virological and resistance outcomes among children initiating first-line ART in sub-Saharan Africa. In this study, we compared virological outcomes in a large cohort of children with moderately advanced HIV disease receiving first-line ART without real-time VL monitoring in Uganda and Zimbabwe. Overall, virological outcomes were good, with almost three-quarters of children on current WHO-recommended abacavir+lamivudine+NNRTI regimens fully suppressed after 4 years of ART and only 6% switching to second-line treatment. We found no evidence of a difference in VL suppression or drug susceptibility between children managed with or without CD4 monitoring. Virological blips were relatively common, but pLLVL and rebound ≥5,000 copies/ml occurred in a minority; only 15% of child-time after week 24 was spent with viraemia in children taking NNRTI+2NRTI regimens. Even among children with VL >1,000 copies/ml, intermediate/high-level drug resistance to key second-line NRTIs was found only in a minority. Children with virological rebound did have a small increase in genotypic NRTI resistance over 2 years. Overall, these results suggest that, where available, annual VL monitoring as recommended by WHO is a reasonable and pragmatic approach in low- and middle-income countries.

The ARROW trial showed that CD4 monitoring (without routine VL monitoring) provided clinical benefit over clinical monitoring alone after the first year on ART. However, event rates were very low (new WHO stage 4 disease/death 0.4 per 100 child-years with CD4 monitoring versus 1.3 without) and 5-year survival was very high (96%). We have now extended these findings, by showing that virological suppression in the cohort as a whole was high. After a median of 4 years, 80% of children randomised to WHO-recommended 2NRTI+NNRTI–based regimens had VL <1,000 copies/ml and 74% had undetectable virus. This is similar to a recent small cohort of Kenyan children monitored for 4 years, in whom two-thirds maintained long-term virological control [16]. Virological suppression from most paediatric [17,18] cohorts falls short of the 90% target set by UNAIDS, highlighting the need for simpler, better-tolerated regimens and effective adherence interventions.

VL did not increase significantly over time in children with pLLVL or rebound; rather, it appeared that viraemia reached an equilibrium (approximately 1,000 and approximately 40,000 copies/ml, respectively), similar to the set-point that is characteristic of untreated HIV infection [19], perhaps due to the capacity for HIV-specific CD8+ T-cell responses to control viral replication on suboptimal ART [20], before potentially changing again to a new equilibrium in the rebound state, driven by further loss of adherence or by immune escape from previously effective T-cell responses [21]. Future studies of HIV-specific T-cell responses in ART-treated children are warranted to investigate these hypotheses further.

Children with virological failure in ARROW had frequent NNRTI and lamivudine resistance, as expected, but retained high susceptibility to both tenofovir and zidovudine, the recommended second-line NRTI options. Perhaps more importantly, a median of 2 years’ viral replication at approximately 40,000 copies/ml led to an increase of only 1 major NRTI mutation and did not substantively alter drug susceptibility. In the PENPACT-1 trial, which compared switch at VL 1,000 versus 30,000 copies/ml in Europe and the Americas, NNRTI resistance had already developed when VL reached >1,000 copies/ml [22], despite 3-monthly VL monitoring. Although NRTI thymidine analogue mutations accumulated with ongoing replication in the 30,000 copies/ml switch threshold group in PENPACT-1, this occurred less frequently in children taking abacavir+lamivudine. Children took a median 80 weeks for VL to increase from 1,000 to 30,000 copies/ml, but all those switching from 2NRTI+NNRTI to second-line at VL >30,000 copies/ml resuppressed within 24 weeks and had similar VL suppression at 5 years compared with those switching at >1,000 copies/ml. Similarly, responses to second-line therapy were good despite modest accumulation of resistance in the Kenyan study [16]. Even when failure is confirmed virologically, clinicians are often reluctant to switch ART because of limited and more complex second-line options (particularly appropriate formulations); limited access to resistance testing to inform decision-making; concerns regarding adherence; and, in resource-limited settings, very limited availability of third-line ART [23]. ARROW provides some reassurance that delays in switching of up to 2 years should have limited implications, particularly since the risk of onward transmission from children is low and the only large randomised trial addressing the role of NRTIs with substantial predicted cross-resistance in second-line treatment suggested they retained considerable activity in adults [7,24].

Over the longer term, substantial efforts are being made to ensure virological monitoring is available in all settings. However, challenges in training, procurement, specimen transport, and financial resources have limited its roll-out [25]. Coverage was estimated at 25% in 2014 [4] and is only estimated to increase to around 47% by 2019 [26]; furthermore, monitoring is mostly restricted to high-level facilities and after the first year is not recommended more often than yearly in most low-income countries. No virological monitoring was undertaken in ARROW; furthermore, VL suppression did not differ between children with or without CD4 monitoring, showing that good virological outcomes are achievable even with clinical monitoring, which can be done at low-level health facilities. Most children switching to second-line ART had detectable VL. Together, these findings highlight that absence of VL monitoring should not be a barrier to providing first-line or switching to second-line ART, given the considerable morbidity and mortality benefits of treatment.

Where virological monitoring is used, it is important to consider the implications of detectable viraemia in children. Current guidelines recommend switching to second-line ART at a confirmed VL above 1,000 copies/ml. However, we found that it was not uncommon for single, or even confirmed, VLs above this threshold to be immediately followed by return to values below the threshold without adherence counselling (since all VLs were measured retrospectively). This was particularly true for VLs between 1,000–5,000 copies/ml—precisely those levels where switch might be considered to have the greatest potential to prevent resistance accumulation. Resuppression on NNRTI-based regimens despite NNRTI resistance has previously been noted in cohorts [27] and a treatment interruption study [28]. This highlights the importance of maximising efforts to extend the durability of first-line ART, for example through enhanced adherence counselling and peer support, given detectable VL. Furthermore, it demonstrates the importance of repeating VL testing before switching from first-line to second-line ART in low-income countries, given the limited treatment regimens available, particularly where VL is 1,000–5,000 copies/ml. Importantly, no children with confirmed VL ≥5,000 copies/ml resuppressed <80 copies/ml. Outside a clinical trial such as ARROW, blips may also be caused by ART interruptions following drug stock-outs. Whilst blips have previously been shown to have no deleterious effect on subsequent VL rebound or CD4 responses [29], their impact on markers of underlying inflammation remains unclear in children and requires further study.

Study limitations include the fact that this was an exploratory analysis within a clinical trial that was conducted using 2006 WHO treatment thresholds, which have now been superseded by universal ART initiation criteria; whether virological outcomes would be different in children treated using current guidelines is unknown. However, given that VLs would be expected to be lower and CD4 percentages higher with earlier treatment, our results plausibly reflect a ‘worst-case’ scenario moving forwards. Genotyping was not conducted at ART initiation, and so may have missed preexisting resistance before ART. A reported 6.8% of those in the WHO African Region with available pre-ART genotypes had 1 or more mutations in any drug class before therapy initiation in 2010 [6], although prevalence of transmitted drug resistance is likely to be considerably lower here, since children were born between 1990–2008. Further resistance could have been identified by sequencing at lower thresholds; all genotyping was performed in Uganda based on a 1,000 copies/ml genotyping threshold. Our study was conducted within a clinical trial where drug supplies were continuous and participants received greater support than in a treatment programme; therefore, incidence of virological failure could have been lower. However, in contrast, most existing paediatric resistance data are from programmes/clinics with real-time VL monitoring; one might expect that resistance may be more prevalent without real-time VL monitoring.

In summary, we found that virological and resistance outcomes were good in this study, and that neither VL suppression nor predicted susceptibility of second-line treatment options were impacted by monitoring with or without CD4 counts over median 4 years follow-up in children initiating ART in Uganda and Zimbabwe. Despite being managed without real-time VL monitoring, only 20% of children on WHO-recommended 2NRTI+NNRTI first-line ART experienced pLLVL or rebound, during which time VL levels were stably maintained over relatively long periods. In rebound, genotypic resistance increased only slightly over 2 years, providing reassurance that annual VL monitoring, as recommended by WHO, is a reasonable and pragmatic approach for HIV-infected children on first-line ART in resource-limited settings.

Supporting Information

Attachment 1

Attachment 2

Attachment 3

Attachment 4

Attachment 5

Attachment 6

Attachment 7

Attachment 8

Attachment 9

Attachment 10


1. Joint United Nations Programme on HIV/AIDS. 90-90-90: an ambitious treatment target to help end the AIDS epidemic. Geneva: 2014.

2. Joint United Nations Programme on HIV/AIDS. AIDS by the numbers. 2016.

3. World Health Organization. Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection: Recommendations for a public health approach. 2016.

4. Joint United Nations Programme on HIV/AIDS. Diagnostics access initiative to achieve the 90-90-90 treatment target. 2015.

5. Sigaloff KCE, Calis JCJ, Geelen SP, van Vugt M, de Wit TFR. HIV-1-resistance-associated mutations after failure of first-line antiretroviral treatment among children in resource-poor regions: a systematic review. Lancet Infect Dis. 2011;11:769–79. doi: 10.1016/S1473-3099(11)70141-4 21872531

6. World Health Organization. WHO HIV drug resistance report 2012. Geneva: 2012.

7. Paton NI, Kityo C, Hoppe A, Reid A, Kambugu A, Lugemwa A, et al. Assessment of Second-Line Antiretroviral Regimens for HIV Therapy in Africa. N Engl J Med. 2014;371(3):234–47. doi: 10.1056/NEJMoa1311274 25014688

8. ARROW Trial team. Routine vs clinically driven laboratory monitoring and first-line antiretroviral therapy strategies in African children with HIV (ARROW): a 5-year open-label randomised factorial trial. Lancet. 2013;381(9875):1391–403. doi: 10.1016/S0140-6736(12)62198-9 23473847

9. Musiime V, Kasirye P, Naidoo-James B, Nahirya-Ntege P, Mhute T, Cook A, et al. Once- versus twice-daily abacavir and lamivudine in African children: the randomised controlled ARROW Trial. AIDS. 2016;30(11):1761–70. doi: 10.1097/QAD.0000000000001116 27064996

10. World Health Organization. Antiretroviral therapy for HIV infection in infants and children: Towards universal access. Recommendations for a public health approach. 2006.

11. Johnson VA, Calvez V, Günthard HF, Paredes R, Pillay D, Shafer RW, et al. Update of the drug resistance mutations in HIV-1: March 2013. Top Antivir Med. 2013;21(1):6–14. 23596273

12. Tang MW, Liu TF, Shafer RW. The HIVdb System for HIV-1 Genotypic Resistance Interpretation. Intervirology. 2012;55:98–101. doi: 10.1159/000331998 22286876

13. World Health Organization. Antiretroviral therapy for HIV infection in infants and children: Towards universal access. Recommendations for a public health approach. 2010.

14. De Onis M, Onyango AW, Borghi E, Siyam A, Nishida C, Siekmanna J. Development of a WHO growth reference for school-aged children and adolescents. Bull World Health Organ. 2007;85:660–7. doi: 10.2471/BLT.07.043497 18026621

15. Wade A, Ades A. Age-related reference ranges: significance tests for models and confidence intervals for centiles. Stat Med. 1994;13:2359–67. 7855469

16. Wamalwa DC, Lehman DA, Benki-Nugent S, Gasper MA, Gichohi R, Maleche-Obimbo E, et al. Long-Term Virologic Response and Genotypic Resistance Mutations in HIV-1 Infected Kenyan Children on Combination Antiretroviral Therapy. J Acquir Immune Defic Syndr. 2013;62(3):267–74. doi: 10.1097/QAI.0b013e31827b4ac8 23196827

17. Sutcliffe CG, van Dijk JH, Bolton C, Persaud D, Moss WJ. Effectiveness of antiretroviral therapy among HIV-infected children in sub-Saharan Africa. Lancet Infect Dis. 2008;8:477–89. doi: 10.1016/S1473-3099(08)70180-4 18652994

18. Ciaranello AL, Chang Y, Margulis AV, Bernstein A, Bassett IV, Losina E, et al. Effectiveness of Pediatric Antiretroviral Therapy in Resource-Limited Settings: A Systematic Review and Meta-analysis. Clin Infect Dis. 2009;49:1915–27. doi: 10.1086/648079 19916798

19. Henrard DL, Phillips JF, Muenz LR, Blatter WA, Wiesner D, Eyster ME, et al. Natural history of HIV-1 cell-free viremia. JAMA. 1995;274(7):554–8. 7629984

20. Mollet L, Li TS, Samri A, Tournay C, Tubiana R, Calvez V, et al. Dynamics of HIV-Specific CD8+ T Lymphocytes with Changes in Viral Load. J Immunol. 2000;165(3):1692–704. 10903781

21. Phillips RE, Rowland-Jones S, Nixon DF, Gotch FM, Edwards JP, Ogunlesi AO, et al. Human immunodeficiency virus genetic variation that can escape cytotoxic T cell recognition. Nature. 1991;354:453–9. doi: 10.1038/354453a0 1721107

22. Harrison L, Melvin A, Fiscus S, Saidi Y, Nastouli E, Harper L, et al. HIV-1 Drug Resistance and Second-Line Treatment in Children Randomized to Switch at Low Versus Higher RNA Thresholds. J Acquir Immune Defic Syndr. 2015;70(1):42–53. doi: 10.1097/QAI.0000000000000671 26322666

23. Davies M-A, Moultrie H, Eley B, Rabie H, Cutsem GV, Giddy J, et al. Virologic Failure and Second-Line Antiretroviral Therapy in Children in South Africa—The IeDEA Southern Africa Collaboration. J Acquir Immune Defic Syndr. 2011;56(3):270–8. doi: 10.1097/QAI.0b013e3182060610 21107266

24. Paton NI, Kityo C, Thompson J, Nankya I, Bagenda L, Hoppe A, et al. Nucleoside reverse-transcriptase inhibitor cross-resistance and outcomes from second-line antiretroviral therapy in the public health approach: an observational analysis within the randomised, open-label, EARNEST trial. Lancet HIV 2017 Aug;4(8):e341–e348. Epub 2017 May 8. doi: 10.1016/S2352-3018(17)30065-6 28495562

25. Lecher S, Ellenberger D, Kim AA, Fonjungo PN, Agolory S, Borget MY, et al. Scale-up of HIV Viral Load Monitoring—Seven Sub-Saharan African Countries. MMWR Morb Mortal Wkly Rep. 2015;64(46):1287–90. doi: 10.15585/mmwr.mm6446a3 26605986

26. Joint United Nations Programme on HIV/AIDS. Ambitious treatment targets: writing the final chapter of the AIDS epidemic. 2014.

27. Hoffmann CJ, Charalambous S, Sim J, Ledwaba J, Schwikkard G, Chaisson RE, et al. Viremia, Resuppression, and Time to Resistance in Human Immunodeficiency Virus (HIV) Subtype C during First-Line Antiretroviral Therapy in South Africa. Clin Infect Dis. 2009;(49):1928–35.

28. Fox Z, Phillips A, Cohen C, Neuhaus J, Baxter J, Emery S, et al. Viral resuppression and detection of drug resistance following interruption of a suppressive non-nucleoside reverse transcriptase inhibitor-based regimen. AIDS. 2008;22(17):2279–89. doi: 10.1097/QAD.0b013e328311d16f 18981767

29. Lee KJ, Shingadia D, Pillay D, Walker AS, Riordan A, Menson E, et al. Transient viral load increases in HIV-infected children in the U.K. and Ireland: what do they mean? Antivir Ther. 2007;12(6):949–56. 17926649

Interní lékařství

Článek vyšel v časopise

PLOS Medicine

2017 Číslo 11

Nejčtenější v tomto čísle

Tomuto tématu se dále věnují…


Zvyšte si kvalifikaci online z pohodlí domova

Antiseptika a prevence ve stomatologii
nový kurz
Autoři: MUDr. Ladislav Korábek, CSc., MBA

Citikolin v neuroprotekci a neuroregeneraci: od výzkumu do klinické praxe nejen očních lékařů
Autoři: MUDr. Petr Výborný, CSc., FEBO

Zánětlivá bolest zad a axiální spondylartritida – Diagnostika a referenční strategie
Autoři: MUDr. Monika Gregová, Ph.D., MUDr. Kristýna Bubová

Diagnostika a léčba deprese pro ambulantní praxi
Autoři: MUDr. Jan Hubeňák, Ph.D

Význam nemocničního alert systému v době SARS-CoV-2
Autoři: doc. MUDr. Helena Lahoda Brodská, Ph.D., prim. MUDr. Václava Adámková

Všechny kurzy
Kurzy Doporučená témata Časopisy
Zapomenuté heslo

Nemáte účet?  Registrujte se

Zapomenuté heslo

Zadejte e-mailovou adresu, se kterou jste vytvářel(a) účet, budou Vám na ni zaslány informace k nastavení nového hesla.


Nemáte účet?  Registrujte se