At the 18th International Workshop on Pediatrics & HIV and AIDS 2026 in Rio de Janeiro, researchers presented new findings spanning epidemiology, prevention of vertical transmission, pediatric treatment, drug resistance, long-acting prevention and treatment, and adolescent care.

Across the findings, a common picture emerged: the science and tools for preventing and treating HIV among women, children, and adolescents continue to improve, but gaps in service delivery are preventing those advances from reaching everyone who could benefit. At the same time, funding instability threatens to widen existing gaps.

Our team reviewed the research.

Five Things That Stood Out

1. Progress is slowing and the remaining gaps require more tailored responses

The decline to approximately 93,000 new HIV infections among children in 2025 represents a major achievement. Yet reaching that milestone took considerably longer than earlier stages of progress.

Line chart titled "Timeline to Get to <100,000 New Annual Infant HIV Infections," showing new HIV infections among children 0-14 from 1990 to 2025. The line rises from about 290,000 in 1990 to a peak of 560,000 around 1999, then declines steadily after maternal ART starts in 2004, reaching 93,000 in 2025. Colored brackets mark four progress periods: 2005-2007 (3 years, 400s→300,000), 2008-2010 (3 years, 300s→200,000), 2011-2014 (4 years, 200s→100,000), and 2015-2024 (10 years, 100s→<100,000), showing the pace of decline has slowed over time. Source: UNAIDS epidemiological estimates 2026.
Source: UNAIDS 2026 Data Report with annotation from Lynne Mofenson.

The remaining burden is highly concentrated. Eastern and Southern Africa accounted for 49% of new pediatric HIV infections in 2025, while Western and Central Africa accounted for another 34%. Together, the two regions accounted for 83% of new pediatric infections globally.

But the drivers of those infections differ substantially by region. In Eastern and Southern Africa, where maternal ART coverage is high, remaining pediatric infections are more often associated with HIV acquisition during pregnancy or breastfeeding, treatment interruption, or lack of viral suppression. In Western and Central Africa, where maternal ART coverage is lower, women not receiving ART during pregnancy or breastfeeding account for a much larger share of new pediatric infections.

Stacked bar chart titled "Causes of New Child Infections Globally 2025 Varies by Region," comparing three bars—Global (93,000), East/Southern Africa (45,300), and West/Central Africa (31,500)—broken down by transmission cause: mother acquired HIV during pregnancy/breastfeeding, mother did not receive ART, mother did not continue ART, and mother on ART but unsuppressed. Globally 42% of infections stem from mothers not receiving ART. In East/Southern Africa, a third of infections come from women acquiring HIV during pregnancy or postpartum; in West/Central Africa, 57% come from women not diagnosed and not receiving ART.
Source: UNAIDS 2026 Data Report with annotation from Lynne Mofenson.

What this means in practice

Accelerating progress will require responses tailored to the gaps driving pediatric infections in different settings. That may mean strengthening earlier diagnosis and ART initiation in some settings, while in others placing greater emphasis on identifying women who acquire HIV during pregnancy or breastfeeding, maintaining women on treatment, and ensuring viral suppression throughout pregnancy and the breastfeeding period. There is no one-size-fits-all solution; the most effective approach will depend on the specific gaps and circumstances in each community.

2. The pediatric treatment gap demands renewed attention, particularly beyond early childhood

While adult ART coverage has continued to increase, pediatric coverage has not kept pace. In 2025, approximately 55% of children ages 0–14 living with HIV were receiving ART, compared with 79% of adults. And that gap appears to be widening.

Line chart titled "Antiretroviral Therapy in Children Continues to Lag Behind Adults," showing ART coverage trends from 2015-2025 for children (0-14, red line) and adults (15+, blue line). Adult coverage rises from about 48% to 79%, while child coverage rises from about 38% to 55%, with shaded confidence bands around each line. A callout notes the gap between children and adults appears to be widening.
Source: UNAIDS 2026 Data Report with annotation from Lynne Mofenson.

Of the estimated 570,000 children living with HIV who were not receiving ART in 2025, 80% were older than age five, underscoring the need to strengthen case finding, linkage, and retention beyond early childhood.

The changing funding environment makes this especially urgent. An analysis of PEPFAR program data found 77,163 fewer children receiving PEPFAR-supported ART in FY2025 than in FY2024, a 14.2% decline. In countries experiencing declines, pediatric reductions outpaced those among adults; in South Africa and India, declines exceeded 40%. The investigators cautioned that these findings are a signal rather than a definitive conclusion, but they raise significant questions about program stability.

Modeling presented at the Pediatric HIV Workshop underscores the potential stakes. If intervention coverage were reduced by 50% by 2030, models project 3 million pediatric HIV infections and 1.1 million deaths by 2040, primarily in sub-Saharan Africa.

What this means in practice

Pediatric treatment trends should be monitored separately from adult trends rather than assuming children will benefit equally from broader ART programs. Particular attention should be paid to finding and retaining older children and adolescents who may be missed by approaches focused primarily on younger children. Programs should also scrutinize site-level enrollment and retention data for early signs that children are disproportionately affected by service disruptions or funding changes. Because pediatric HIV programs depend on functioning health systems, reliable supply chains, and sustained investment, declines in pediatric treatment may also provide an early warning, a canary-in-the-coal-mine, of broader program disruption.

3. Closing the PMTCT gaps requires reaching women beyond facility visits

Several studies presented in Rio showed how gaps can emerge even where PMTCT services are well established. An audit of 365 infants who acquired HIV in Uganda found that nearly half of their mothers were first diagnosed with HIV during breastfeeding. Only about half of the infants had documented postnatal ARV prophylaxis. Maternal viral load and partner testing were also significant gaps.

Slide titled "Missed Opportunities in PMTCT Cascade in Uganda, 2021-2025: Detection by Routine HIV Infant Audits" (Nabitaka L., IAS AIDS 2026, Abs. OAC1303), summarizing a chart audit of 365 infants who acquired HIV. Four panels show: a bar chart of timing of maternal HIV diagnosis (most diagnosed during breastfeeding, 158 cases/43.3%); maternal viral load documentation at only 37%, with 29% of those tested not virally suppressed; partner HIV testing known in only 29.3% of cases; and infant postnatal prophylaxis documented in 51.2% of cases.
Source: Nabitaka L. International AIDS Conference Rio de Janeiro, Brazil 2026 Abs. OAC1303

Examples of solutions to these challenges provided cause for optimism. Studies in Nigeria and India demonstrated how community-based and decentralized approaches—including working through traditional birth attendants, faith-based facilities, lower-level health facilities, and community health workers—can bring HIV testing and linkage closer to pregnant women who may not be reached through traditional facility-based services.

Slide titled "Closing Gaps Through Community-Based ANC Services, Traditional Birth Attendants & Faith-Based Delivery Settings, Nigeria" (Ajuka-Patrick V., IAS AIDS 2026, Abs. OAC13104). Shows testing coverage of 331,873 pregnant women (94.9% average across 7 states, ranging from 87.0% in Jigawa to 99.0% in Zamfara) with a bar chart by state; HIV positivity of 464 women (0.14%), highest in Kaduna (0.40%) and lowest in Katsina (0.02%), shown in a state-by-state bar chart; and linkage to ART, with 285 women linked (61.4% overall, 100% in Kebbi and Zamfara, lowest 5.4%/0% in Sokoto and Jigawa), plus a bar chart of ART timing during pregnancy. A quote box states the program tapped into existing community-based maternity care to create an HIV prevention model.
Ajuka-Patrick V., International AIDS Conference, Rio de Janeiro, Brazil, 2026, Abs. OAC13104

Postpartum monitoring remains another important vulnerability. Data from the Western Cape showed increased viral load testing during pregnancy following updated guidelines and the rollout of dolutegravir, driven largely by increased testing at delivery. But postpartum monitoring did not show the same improvement.

What this means in practice

The PMTCT cascade cannot effectively end at delivery. Programs should examine whether testing, prophylaxis, viral load monitoring, and retention systems adequately cover pregnancy and the full breastfeeding period, while considering community-based and differentiated models for populations poorly reached through facility-based services.

4. Better pediatric HIV treatment still depends on finding treatment failure early

Dolutegravir (DTG)-based ART has significantly improved treatment options for children living with HIV. Evidence presented in Rio supports its effectiveness. But even highly effective treatment does not eliminate treatment failure. This underscores the importance of identifying and responding quickly when viral load remains high.
Among children and young people with confirmed viral failure while receiving DTG, researchers found evidence of drug resistance in many of those tested. This included resistance to the class of drugs that includes DTG.

Other findings were reassuring. In the PENTA-21 study, children who were already virally suppressed and switched to dolutegravir/lamivudine (DTG/3TC) maintained high levels of viral suppression, including those with evidence of previous drug resistance.

Slide titled "Viral Suppression and Predictors of Failure Following DTG ART Optimization in 5 Eastern/Southern Pediatric Centers (Baylor)" (Perry SH., IAS AIDS 2026, Abs. WEPEB112). A Sankey diagram shows viral load flow for 13,092 children/adolescents (ages 0-24) before and after switching to dolutegravir (DTG): most with pre-DTG VL ≤50 remained suppressed post-DTG, while those with higher pre-DTG viral loads had more post-DTG viral failure (8.3% to 8.5% confirmed failure). A multivariable table lists risk factors for viral failure, including age 10-19 years, female sex, higher pre-DTG viral load, switching from a PI-based regimen, concurrent TB treatment or cation use, and country (highest odds in Botswana and Eswatini). Conclusions note DTG reduced viral failure in younger children but rates in older children still exceed 5%.
Perry SH., International AIDS Conference, Rio de Janeiro, Brazil, 2026, Abs. WEPEB112

What this means in practice

DTG-based treatment remains highly effective, but programs cannot assume that an effective regimen alone eliminates treatment failure. Regular viral load monitoring, prompt follow-up when viral load remains high, and adherence and differentiated care support remain essential.

5. How services are delivered to adolescents may be as important as what is delivered

Some of the most promising findings presented in Rio involved long-acting prevention and treatment. In the LATA trial, adolescents living with HIV who were virally suppressed were randomized to receive either long-acting injectable cabotegravir/rilpivirine or daily oral tenofovir/lamivudine/dolutegravir (TLD). At 96 weeks, confirmed viral rebound was less common among adolescents receiving the long-acting regimen than among those receiving daily oral TLD. The injectable regimen was also well tolerated and strongly preferred by participants, with 99% of maintenance injections given on time.

Slide titled "LA-CAB/RPV ART Superior to Daily Oral TLD in Adolescents: LATA 96-Week Results" (Bwakura Dangarembizi MB., IAS AIDS 2026, Abs. OAX1105LB). An FDA snapshot bar chart at week 96 shows 94.9% of the long-acting injectable (LAI) group and 93.8% of the oral TLD control group had HIV-1 RNA <50 copies/mL, with an adjusted difference of -2.8% favoring LAI/CAB-RPV (p=0.018). A forest plot shows differences in confirmed viral rebound at thresholds of ≥50, ≥200, and ≥1000 copies/mL, generally favoring LAI. Tables show comparable adverse event rates between arms and pregnancy outcomes (34/476, 7%) by treatment choice. A pie chart shows 94% of adolescents on LAI found injections "a lot easier" than daily pills. The slide concludes CAB/RPV was superior to TLD over 96 weeks, well-tolerated, and strongly preferred by adolescents living with HIV.
Source: Bwakura Dangarembizi MB., International AIDS Conference, Rio de Janeiro, Brazil, 2026, Abs. OAX1105LB

Evidence on long-acting PrEP also reinforces an important implementation lesson: biomedical innovation alone is not enough. Among adolescent girls, young women, and female sex workers using long-acting cabotegravir for PrEP in Zambia, community-based delivery was associated with a substantially lower risk of discontinuation than facility-based delivery. The investigators concluded that delivery model, not simply dosing frequency, was a major determinant of persistence.

What this means in practice

New long-acting technologies could substantially expand the options available to adolescents and young people, but their impact will depend on delivery models that reflect how young people actually engage with services. Community delivery and differentiated care should be prioritized alongside biomedical innovation. Adequate resources will also be essential to translate these innovations into effective, sustainable programs.

Taking this knowledge forward

The science presented in Rio shows us that the next phase of the pediatric and maternal HIV response will require programs to focus more deliberately on the populations and moments where current systems are losing people: from early access to antenatal care, where community-based models remain essential to reach women who would otherwise miss testing altogether, through maternal diagnosis during breastfeeding and postpartum viral load monitoring to case finding among older children and retention of adolescents in treatment and prevention services. At the same time, funding instability threatens to widen precisely the pediatric treatment gaps the global HIV response has spent decades trying to close.

But we know progress, even during the most challenging times, is possible.

The global HIV response has already driven dramatic reductions in new pediatric infections by translating effective interventions into programs that reach women and children. We know what sustained commitment can achieve. The challenge now is to bring that same urgency and resolve to the gaps that remain, tailoring programs to reach those being missed, protecting hard-won gains, and accelerating progress toward a generation in which no child acquires HIV.


This review was conducted by Dr. Lynne Mofenson, senior technical advisor, and Dr. Roland van de Ven, senior director, technical excellence, with support from Glassroth Creative Strategies.