Evidence map›Paper›PMID 41791199›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2026

Characterization of HIV humoral immunity during analytical treatment interruption.

Clara Di Germanio, Brendan G Balasko, Patricia G Villaflor, George Noutsios, Jonathan Z Li, Davey M Smith, Steven Deeks, Ronald J Bosch, Rajesh T Gandhi, Philip J Norris and 1 more

Abstract read
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Clara Di GermanioVitalant Research Institute, San Francisco, CA, United States; University of California San Francisco, San Francisco, CA, United States. Electronic address: cdigermanio@vitalant.org.
Brendan G BalaskoVitalant Research Institute, San Francisco, CA, United States. Electronic address: bbalasko@vitalant.org.
Patricia G VillaflorVitalant Research Institute, San Francisco, CA, United States. Electronic address: pvillaflor@vitalant.org.
George NoutsiosBio-Rad Laboratories, Clinical Immunology Diagnostics, Hercules, CA, United States. Electronic address: georgios_noutsios@bio-rad.com.
Jonathan Z LiBrigham and Women's Hospital, Harvard Medical School, Boston, MA, United States. Electronic address: JLI@BWH.HARVARD.EDU.
Davey M SmithUniversity of California San Diego, San Diego, CA, United States. Electronic address: d13smith@health.ucsd.edu.
Steven DeeksUniversity of California San Francisco, San Francisco, CA, United States. Electronic address: Steven.Deeks@ucsf.edu.
Ronald J BoschHarvard T. H. Chan School of Public Health, Boston, MA, United States. Electronic address: ronbosch@sdac.harvard.edu.
Rajesh T GandhiMassachusetts General Hospital, Harvard Medical School, Boston, MA, United States. Electronic address: RGANDHI@mgh.harvard.edu.
Philip J NorrisVitalant Research Institute, San Francisco, CA, United States; University of California San Francisco, San Francisco, CA, United States. Electronic address: PNorris@vitalant.org.
Michael P BuschVitalant Research Institute, San Francisco, CA, United States; University of California San Francisco, San Francisco, CA, United States. Electronic address: mbusch@vitalant.org.

Funding

Leadership and Operations Center (LOC), AIDS Clinical Trials Group (ACTG); LOC 1/UM1AI068636 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, RAJESH T GANDHI · 2011 to 2026
$1073.1M
Statistical and Data Management Center (SDMC), AIDS Clinical Trials Group (ACTG)UM1AI068634 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Marlene Ann Cooper, Michael David Hughes · 2011 to 2026
$246.6M
Validation, CLIA and Qualification (VQC): Enhancing the RS ratio as a tool for AIDS Clinical Trial Group (ACTG) tuberculosis trialsUM1AI106701 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Grace M Aldrovandi · 2014 to 2026
$116.8M
UCSD Department of Medicine HIV/AIDS Clinical Trials UnitUM1AI069432 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TIMOTHY J. WILKIN · 2012 to 2026
$50.4M
San Francisco Vaccine and Prevention UnitUM1AI069496 · NIAID · PUBLIC HEALTH FOUNDATION ENTERPRISES · PI Susan Buchbinder, Diane V Havlir · 2012 to 2026
$30.5M
High-Definition Characterization of the Persistence and Perturbation of the HIV Reservoir: Project 3P01AI169768 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Ya-Chi Ho, Jonathan Li · 2022 to 2026
$10.1M
NIAID NIH HHS P01 AI169768NIAID NIH HHS UM1 AI068634NIAID NIH HHS UM1 AI068636NIAID NIH HHS UM1 AI069432NIAID NIH HHS UM1 AI069496NIAID NIH HHS UM1 AI106701
6 · The paper itself

Abstract

introductionThis study investigated whether HIV binding antibody (Ab) and p24 antigen (Ag) quantitation could detect humoral immune responses or p24 Ag before or following detectable plasma viral load (VL) rebound during antiretroviral therapy interruption (ATI) and provide insights into post-rebound viral replication.

methodsLongitudinal plasma samples collected before and following ATI from 40 participants (485 samples; mean of 12/participant) in the ACTG A5345 study who began antiretroviral therapy during either acute or chronic stages of infection were analyzed using commercial immunoassays to assess HIV Ab and Ag dynamics, including following dissociation of immune complexes for improved Ag detection.

resultsNeither Ab nor Ag levels increased in plasma before VL rebound. However, 75% of participants exhibited increased Ab reactivity concurrent with or shortly after VL rebound, which declined upon ART reinitiation. Participants who were ART-treated early had lower Ab levels at ATI initiation but demonstrated greater fold increases in Ab during ATI than late-treated participants. Two participants who demonstrated post-treatment control of VL showed gradual Ab increases that paralleled intermittent VL elevations. p24 Ag was only detectable after dissociating immune complexes in samples with VL > 10⁴ RNA copies/mL, correlating strongly with VL levels.

conclusionsAlthough antibody levels did not predict viral rebound, tracking their longitudinal changes provided meaningful information about viral replication patterns and immune reactivation during and after rebound, offering a practical tool for monitoring ATI outcomes.

Indexed as

Anti-HIV AgentsHIV-1HIV AntibodiesHIV InfectionsImmunity, HumoralAdultFemaleHIV Core Protein p24HumansLongitudinal StudiesMaleTreatment InterruptionViral LoadAnti-HIV AgentsHIV AntibodiesHIV Core Protein p24Analytical treatment interruptionAntibodyViral rebound

Identifiers

PMID41791199
PMCPMC13055523

What OpenQuestion holds

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Registered trials

None linked

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.