Evidence map›Paper›PMID 41589894›Full record

ArticleJournal of virology2026

Retinoids enhance NK effector function against HIV-infected CD4 T cells.

Elyse K McMahon, Jonathan S Lochner, Rebecca M Lynch, Alberto Bosque

Abstract read
In one paragraph

Article in Journal of 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

4 authors.

Elyse K McMahonDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA.
Jonathan S LochnerDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA.
Rebecca M LynchDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA.
Alberto BosqueDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA.ORCID 0000-0002-8800-2160

Funding

REACH: Research Enterprise to Advance a Cure for HIVUM1AI164565 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI Marina Caskey, R. Brad Jones · 2021 to 2026
$32.9M
Cancer Biology Training Program (CBTP)T32CA247756 · NCI · GEORGE WASHINGTON UNIVERSITY · PI LEE, NORMAN H, SETO, EDWARD · 2020 to 2024
$1.4M
Training in HIV Persistence, Co-morbidities and TherapeuticsT32AI158105 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BOSQUE, ALBERTO, MAGGIRWAR, SANJAY B. · 2021 to 2025
$909k
Pathways modulating memory-like properties in NK cells and their impact on HIV controlR21AI172042 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BOSQUE, ALBERTO · 2022 to 2023
$444k
NCI NIH HHS T32 CA247756NIAID NIH HHS R21 AI172042NIAID NIH HHS T32 AI158105NIAID NIH HHS UM1 AI164565
6 · The paper itself

Abstract

Novel approaches to sensitize latently infected cells to apoptosis may provide additional methods to eliminate latent reservoirs. Prior research identified several retinoids as potential drugs that increase the sensitivity of HIV-infected cells to cell death. Retinoids are derivatives of vitamin A that target retinoid receptors causing antiproliferative and proapoptotic activity. Several are FDA-approved or in clinical trials. The aim of this study was to evaluate the ability of vitamin A, three of its natural metabolites, and nine synthetic derivatives to sensitize HIV-infected CD4 T cells to NK natural cytotoxicity and antibody-dependent cellular cytotoxicity (ADCC). From the retinoids tested, alitretinoin, tazarotene acid, and AM80 significantly enhanced NK natural cytotoxicity in the presence of IL-15. Mechanistically, these retinoids increased NK degranulation upon target recognition in an HLA-F/KIR3DS1-dependent manner. Furthermore, these retinoids enhanced ADCC by transcriptionally increasing CD16 expression on NK cells. In conclusion, our study has identified at least three retinoids capable of enhancing NK natural cytotoxicity and ADCC against HIV-infected cells. These or other retinoids could be used to reduce HIV persistent reservoirs.IMPORTANCEThis study highlights how retinoids, compounds derived from vitamin A, can help the immune system target HIV-infected cells more effectively. HIV often hides in immune cells, making it difficult to fully eliminate the virus. We found that certain retinoids, including alitretinoin, tazarotene acid, and AM80, improve the function of natural killer (NK) cells-key immune cells that target infected cells. These retinoids boost NK cell activity by increasing their ability to release toxic molecules that kill infected cells and by enhancing their response to antibodies targeting HIV. This makes the infected cells more vulnerable to being eliminated. Since some of these retinoids are already approved for medical use, they could offer a promising way to reduce persistent HIV reservoirs in the body and improve efforts to cure the infection.

Indexed as

CD4-Positive T-LymphocytesHIV-1HIV InfectionsKiller Cells, NaturalRetinoidsAlitretinoinAntibody-Dependent Cell CytotoxicityBenzoatesHumansNicotinic AcidsTetrahydronaphthalenesAlitretinoinBenzoatesNicotinic AcidsRetinoidstamibarotenetazaroteneTetrahydronaphthalenesHIVHLA-FIL-15KIR3DS1natural killer cellsNKretinoids

Identifiers

PMID41589894
PMCPMC12911896

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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.