Evidence map›Paper›PMID 40471871›Full record

ArticleJCI insight2025

Impact of the IL-15 superagonist N-803 on lymphatic reservoirs of HIV.

Joshua Rhein, Jeffrey G Chipman, Gregory J Beilman, Ross Cromarty, Kevin Escandón, Jodi Anderson, Garritt Wieking, Jarrett Reichel, Rodolfo Batres, Alexander Khoruts and 13 more

Registry-linked trialAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in JCI insight, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04808908 (Effect of N-803 on B Cell Follicles in Antiretroviral Treated HIV Disease), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT04808908 phase1completednot on this map

Effect of N-803 on B Cell Follicles in Antiretroviral Treated HIV Disease

TypeinterventionalSponsorUniversity of MinnesotaRan2021 to 2023Enrolled10ConditionsHiv, HIV Infections, AIDSArmsN-803
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. CXCR6Frontiers in immunology · 2026
    Article
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

23 authors.

Joshua RheinDivision of Infectious Diseases and International Medicine, Department of Medicine.
Jeffrey G ChipmanDepartment of Surgery.
Gregory J BeilmanDepartment of Surgery.
Ross CromartyMasonic Cancer Center.
Kevin EscandónDivision of Infectious Diseases and International Medicine, Department of Medicine.
Jodi AndersonDivision of Infectious Diseases and International Medicine, Department of Medicine.
Garritt WiekingDivision of Infectious Diseases and International Medicine, Department of Medicine.
Jarrett ReichelDivision of Infectious Diseases and International Medicine, Department of Medicine.
Rodolfo BatresDivision of Infectious Diseases and International Medicine, Department of Medicine.
Alexander KhorutsDivision of Gastroenterology, Department of Medicine.
Christopher M BastingDepartment of Surgery.
Peter HinderlieDivision of Hematology, Oncology, and Transplantation, Department of Medicine; and.
Zachary B DavisDivision of Hematology, Oncology, and Transplantation, Department of Medicine; and.
Anne EatonDivision of Biostatistics and Health Data Science, School of Public Health, University of Minnesota, Minneapolis, Minnesota, USA.
Byron P VaughnDivision of Gastroenterology, Department of Medicine.
Elnaz EilkhaniDivision of HIV, Infectious Diseases and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.
Jeffrey T SafritImmunityBio, Culver City, California, USA.
Patrick Soon-ShiongImmunityBio, Culver City, California, USA.
Jason V BakerDivision of Infectious Diseases and International Medicine, Department of Medicine.
Nichole R KlattDepartment of Surgery.
Steven G DeeksDivision of HIV, Infectious Diseases and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.
Jeffrey S MillerMasonic Cancer Center.
Timothy W SchackerDivision of Infectious Diseases and International Medicine, Department of Medicine.

Funding

Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
Reversing Immune Dysfunction for HIV-1 EradicationUM1AI164561 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI SUMIT K CHANDA, Paula M Cannon · 2021 to 2026
$30.0M
Delaney AIDS Research Enterprise to Cure HIVUM1AI126611 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEEKS, STEVEN GRANT, PICKER, LOUIS J. · 2016 to 2020
$27.9M
Investigation of persistent HIV immune stimulation in lymphoid tissues during therapy as a cause of sustained immune activationR01AI147912 · NIAID · UNIVERSITY OF MINNESOTA · PI SCHACKER, TIMOTHY W · 2020 to 2024
$3.7M
Targeting off-the-shelf iPSC-derived natural killer cells against solid tumorsR35CA283892 · NCI · UNIVERSITY OF MINNESOTA · PI Jeffrey S. Miller · 2023 to 2026
$3.7M
NCATS NIH HHS UL1 TR002494NCI NIH HHS P01 CA065493NCI NIH HHS R35 CA283892NIAID NIH HHS R01 AI147912NIAID NIH HHS UM1 AI126611NIAID NIH HHS UM1 AI164561
6 · The paper itself

Abstract

BACKGROUNDNK cell function is impaired in people with HIV (PWH), hindering their potential to reduce the lymphoid tissue (LT) reservoir. The IL-15 superagonist N-803 has been shown to enhance NK and T cell function and thus may reduce viral reservoirs.METHODSTo determine the impact of N-803 on LTs, we conducted a clinical trial where 10 PWH on effective antiretroviral therapy (ART) were given 3 subcutaneous 6 mcg/kg doses of N-803. We obtained PBMCs and lymph node (LN) and gut biopsies at baseline and after the last N-803 dose.RESULTSWe found a nonstatistically significant approximately 0.50 median log reduction in the frequency of viral RNA+ (vRNA+) and vDNA+ cells/g in the 6 participants with baseline and posttreatment LN biopsies. In the ileum, we observed reductions of vRNA+ cells in 8/10 participants and vDNA+ cells in all participants. We also found significant inverse correlations between NK cell proliferation and the frequency of vRNA+ cells and between NKG2A expression on NK cells and the frequency of vRNA+ cells.CONCLUSIONOur findings suggest N-803 may reduce the HIV reservoir in LTs of PWH on ART, an effect likely mediated by enhanced NK cell function. Controlled studies assessing the impact of NK cell therapy on HIV LTs are needed.TRIAL REGISTRATIONClinicalTrials.gov NCT04808908.FUNDINGNIH grants 5UM1AI126611, UL1TR002494, R01 AI147912, R35 CA283892, and UM1AI164561.

Indexed as

HIV-1HIV InfectionsInterleukin-15Lymphoid TissueAdultFemaleHumansKiller Cells, NaturalLymph NodesMaleMiddle AgedRecombinant Fusion ProteinsRNA, ViralViral LoadALT-803IL15 protein, humanInterleukin-15Recombinant Fusion ProteinsRNA, ViralAIDS/HIVImmunotherapyInfectious diseaseNK cells

Identifiers

PMID40471871
PMCPMC12288898

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Registered trials

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.