Evidence map›Paper›PMID 41574287›Full record

ArticleImmunotherapy advances2026

Targeting intratumoral regulatory T cells by CD137 aptamer-shRNA chimeras.

Kang Yi Lee, Yu Mei, Haiyan Liu, Herbert Schwarz

Abstract read
In one paragraph

Article in Immunotherapy advances, 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.

Kang Yi LeeNUS Immunology Programme, Life Sciences Institute, Department of Microbiology and Immunology, National University of Singapore, 117545 Singapore, Singapore.
Yu MeiNUS Immunology Programme, Life Sciences Institute, Department of Microbiology and Immunology, National University of Singapore, 117545 Singapore, Singapore.
Haiyan LiuNUS Immunology Programme, Life Sciences Institute, Department of Microbiology and Immunology, National University of Singapore, 117545 Singapore, Singapore.
Herbert SchwarzNUS Immunology Programme, Life Sciences Institute, Department of Microbiology and Immunology, National University of Singapore, 117545 Singapore, Singapore.ORCID https://orcid.org/0000-0002-3558-3424

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The cytokine CD137 (TNFRSF9, 4-1BB) is best known as a T cell costimulatory molecule. However, CD137 is also part of a negative feedback mechanism that limits T cell activation, and that is employed by regulatory T cells (Tregs) to prevent an overstimulation of T cells and subsequent autoimmune damage. CD137 has been identified as the gene that most significantly distinguishes intra- from extratumoral Tregs. CD137 Methods and Results: We fused the aptamer to short hairpin (sh) RNAs that are specific for Enhancer of zeste homolog 2 (EzH2) or neuropilin-1 (Nrp1), and demonstrated their uptake into CD137 Conclusion: This study confirms CD137 as a target for tumor immunotherapy and introduces CD137 aptamer-shRNA chimeras as novel tools to be evaluated for their usefulness in cancer treatment.

Indexed as

aptamerCD137enhancer of zeste homolog 2neuropilin-1regulatory T cellsshort hairpin RNA

Identifiers

PMID41574287
PMCPMC12822494

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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.