Evidence map›Paper›PMID 41313002›Full record

ArticleJournal of virology2025

The functional antibody landscape in HIV post-treatment controllers is heterogeneous.

Nicholas E Webb, Matthew J Gorman, Lily J Parker, Wonyeong Jung, Dansu Yuan, Jonathan Z Li, Galit Alter, Boris Julg

Abstract read
In one paragraph

Article in Journal of virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

8 authors.

Nicholas E WebbRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.ORCID 0000-0003-4370-553X
Matthew J GormanRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.
Lily J ParkerRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.
Wonyeong JungRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.
Dansu YuanRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.
Jonathan Z LiBrigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Galit AlterRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.
Boris JulgRagon Institute of Mass General MIT and Harvard, Cambridge, Massachusetts, USA.ORCID 0000-0002-4687-9626

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
Delaney AIDS Research Enterprise to Cure HIVUM1AI164560 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS, Sharon Ruth Lewin · 2021 to 2026
$32.0M
I4C 2.0: Immunotherapy for CureUM1AI164556 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Dan H. Barouch, John W Mellors · 2021 to 2026
$28.0M
NHP CoreP01AI177687 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Dan H. Barouch · 2023 to 2026
$7.4M
HIV Reservoir Ecology of Viral Remission (PTC)R01AI150396 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI LI, JONATHAN · 2020 to 2025
$5.4M
Demystifying the antiviral activity of the IgG3+ antibody responseR01AI080289 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI JUELG, BORIS DOMINIK · 2009 to 2024
$4.1M
HIV Reservoir Ecology of Viral Remission (PTC)R37AI150396 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Jonathan Li · 2026 to 2026
$868k
NIAID NIH HHS P01 AI177687NIAID NIH HHS R01 AI080289NIAID NIH HHS R01 AI150396NIAID NIH HHS R37 AI150396NIAID NIH HHS UM1 AI068634NIAID NIH HHS UM1 AI068636NIAID NIH HHS UM1 AI106701NIAID NIH HHS UM1 AI164556NIAID NIH HHS UM1 AI164560
6 · The paper itself

Abstract

HIV-1 establishes a latent reservoir early in infection that persists during antiretroviral therapy (ART), typically leading to rapid viral rebound upon treatment interruption in most people living with HIV-1. However, a rare group known as post-treatment controllers (PTCs) can maintain low or undetectable viral loads for extended periods after ART cessation, offering critical insights into durable HIV remission. While immune responses are thought to play a key role in this control, the contribution of humoral immunity-particularly Fc-mediated antibody functions-remains insufficiently defined. In this study, we explored the influence of humoral responses on viral rebound in PTCs using a comprehensive systems serology approach. We profiled Env-specific antibody characteristics and Fc-effector functions-including antibody-dependent cellular phagocytosis, antibody-dependent neutrophil phagocytosis, antibody-dependent complement deposition, and antibody-dependent NK cell activation-in PTCs and matched non-controllers (NCs). Baseline antibody features prior to ART interruption did not clearly distinguish PTCs from NCs, and antibody responses evolved dynamically and in a highly individualized manner during viral rebound. Notably, distinct and individual-specific shifts in Fc-functional antibody signatures occurred during rebound, indicating that the humoral immune system actively adapts during this critical period. These findings highlight the complexity and adaptability of antibody-mediated responses, shaped by dynamic processes during rebound rather than static baseline features. This work underscores the value of longitudinal immune profiling to delineate how humoral immunity evolves in relation to, but not necessarily driving, post-treatment control.IMPORTANCEMost people living with HIV experience a quick return of the virus after stopping antiretroviral therapy (ART). However, a small group-post-treatment controllers (PTCs)-can keep the virus suppressed without ongoing treatment. This study examined whether antibody responses, especially those involving Fc-mediated functions, play a role in this control. This study compared antibody features and immune functions in PTCs and matched individuals who did not control the virus after stopping ART. They found that antibody profiles before treatment interruption did not predict who would control the virus. Instead, antibody responses changed over time in unique ways during viral rebound. These shifts suggest that the immune system adapts dynamically rather than relying on fixed traits. The findings highlight the importance of tracking immune changes over time to better understand how long-term HIV control may occur, even if antibodies alone may not be the driving force behind post-treatment remission.

Indexed as

HIV-1HIV AntibodiesHIV InfectionsHIV Long-Term SurvivorsAdultFemaleHumansImmunity, HumoralKiller Cells, NaturalMaleMiddle AgedPhagocytosisViral LoadHIV Antibodiesantibody responsesHIV-1post-treatment controllerssystem serology

Identifiers

PMID41313002
PMCPMC12724254

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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.