Evidence map›Paper›PMID 41891213›Full record

ArticleAIDS (London, England)2026

Increases in total HIV-1 nucleic acid in whole blood precede plasma RNA rebound during pediatric analytical treatment interruption.

Gabriela Z L Cromhout, Nomonde Bengu, Nicholas G Herbert, Rowena Fillis, Samantha Kannie, Jeroen Van Lobenstein, Kogielambal Chinniah, Malini Krishna, Roopesh Bhoola, Noxolo Mahlaba and 6 more

Abstract read
In one paragraph

Article in AIDS (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Gabriela Z L CromhoutHIV Pathogenesis Programme, Doris Duke Medical Research Institute, Nelson R Mandela School of Medicine.
Nomonde BenguHIV Pathogenesis Programme, Doris Duke Medical Research Institute, Nelson R Mandela School of Medicine.
Nicholas G HerbertPeter Medawar Building for Pathogen Research, Department of Paediatrics, University of Oxford, Oxford, UK.
Rowena FillisHarry Gwala Regional Hospital, Pietermaritzburg.
Samantha KannieGeneral Justice Gizenga Mpanza Regional Hospital, KwaDukuza.
Jeroen Van LobensteinGeneral Justice Gizenga Mpanza Regional Hospital, KwaDukuza.
Kogielambal ChinniahMahatma Gandhi Memorial Hospital.
Malini KrishnaHarry Gwala Regional Hospital, Pietermaritzburg.
Roopesh BhoolaHarry Gwala Regional Hospital, Pietermaritzburg.
Noxolo MahlabaHarry Gwala Regional Hospital, Pietermaritzburg.
Maria C Garcia-GuerreroIrsiCaixa, Badalona, Barcelona.
Thumbi Ndung'uDepartment of Paediatrics and Child Health, University of KwaZulu-Natal, Durban.
Maria C PuertasIrsiCaixa, Badalona, Barcelona.
Javier Martinez-PicadoIrsiCaixa, Badalona, Barcelona.
Moherndran ArcharyDepartment of Paediatrics and Child Health, University of KwaZulu-Natal, Durban.
Philip J R GoulderHIV Pathogenesis Programme, Doris Duke Medical Research Institute, Nelson R Mandela School of Medicine.

Funding

LOC-IMPAACT Leadership GroupPharmacokinetics and Safety of Remdesivir for Treatment of COVID-19 in Pregnant Women in the USUM1AI068632 · NIAID · SOCIAL AND SCIENTIFIC SYSTEMS, INC. · PI Jennifer Jao, Sharon A Nachman · 2011 to 2026
$278.1M
Statistical and Data Management Center-Pediatric,Adolescent, and Maternal CTGUM1AI068616 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Sean Scott Brummel, Marlene Ann Cooper · 2011 to 2026
$155.6M
NIAID NIH HHS UM1 AI068616NIAID NIH HHS UM1 AI068632
6 · The paper itself

Abstract

objectivesIn the absence of reliable biomarkers, analytical treatment interruption (ATI) is needed to evaluate HIV-1 cure/remission strategies. Children living with HIV-1 may have high potential to achieve cure/remission due to very-early antiretroviral therapy (ART) initiation combined with early-life immunity. However, pediatric ATI safety monitoring requires frequent blood sampling for early plasma viral rebound detection to facilitate prompt ART resumption.

designWe hypothesized that viral rebound during ATI would be detected earlier by point-of-care (PoC) total HIV-1 nucleic acid (TNA) measurement, which quantifies both HIV-1 RNA and DNA, than via standard laboratory assays of plasma HIV-1 RNA. Therefore, viral rebound during pediatric ATI studies could be detected earlier via a practical and user-friendly approach.

methodsNineteen very-early ART-treated children underwent ATI. Sixteen experienced plasma HIV-1 viral rebound. PoC TNA testing with the Cepheid GeneXpert HIV-1 Qual XC assay, requiring 100 μl of whole blood and 2 h turnaround time (TAT), was compared with standard plasma HIV-1 RNA quantification (Aptima Quant), requiring 500 μl of whole blood and 30 h TAT.

resultsGeneXpert TNA Ct values and plasma HIV-1 RNA were strongly negatively correlated ( r  = -0.88, P  < 0.0001). In all 27 instances where viral rebound was detected by plasma HIV-1 RNA testing, TNA was also detected. In 12 instances, TNA was detected prior to any plasma RNA rebound. There were no instances where plasma rebound was detected prior to TNA detection ( P  = 2 x 10 -15 ).

conclusionPoC HIV-1 TNA testing offers a more rapid and lower-volume method to detect viral rebound in pediatric ATI, enhancing safety monitoring and timely ART reinitiation.

Indexed as

Anti-Retroviral AgentsHIV-1HIV InfectionsPlasmaRNA, ViralViral LoadAdolescentChildChild, PreschoolFemaleHumansInfantMaleRapid Diagnostic TestsTreatment InterruptionAnti-Retroviral AgentsRNA, ViralAfricaanalytical treatment interruptionantiretroviral therapycure/remissionHIVHIV-1HIV replicationpediatricspoint-of-care testing

Identifiers

PMID41891213
PMCPMC13336579

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.