Evidence map›Paper›PMID 42120791›Full record

ArticleNature immunology2026

Epigenetic reprogramming of T cell metabolism restores function and enhances anti-tumor immunity in lung cancer.

Yi-Chieh Wu, Shih-Feng Yang, Yu-Ting Lee, Meng-Wei Chou, Shu-Yung Lin, Yu-Ching Wang, Sheng-Yao Su, Chia-Lang Hsu, Nai-Wen Chang, Yi-Jhen Huang and 13 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 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

23 authors.

Yi-Chieh WuGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Shih-Feng YangGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Yu-Ting LeeGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Meng-Wei ChouGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Shu-Yung LinDepartment of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
Yu-Ching WangGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Sheng-Yao SuGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Chia-Lang HsuDepartment of Medical Research, National Taiwan University Hospital, Taipei City, Taiwan.ORCID http://orcid.org/0000-0002-7447-8045
Nai-Wen ChangDepartment of Medical Research, National Taiwan University Hospital, Taipei City, Taiwan.
Yi-Jhen HuangGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Yi-Hsiu JuanDepartment of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
Hsuan-Hsuan LuDepartment of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.ORCID http://orcid.org/0000-0002-2398-9347
Chien-Yin ChenInstitute of Molecular Medicine, National Taiwan University College of Medicine, Taipei City, Taiwan.
Yi-Fu WangInstitute of Biomedical Sciences, Academia Sinica, Taipei City, Taiwan.ORCID http://orcid.org/0009-0003-2387-9353
Po-Ju LeeTaiwan International Graduate Program in Molecular Medicine, National Yang Ming Chiao Tung University and Academia Sinica, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-7369-2015
Hsiao-Jung KaoInstitute of Biomedical Sciences, Academia Sinica, Taipei City, Taiwan.ORCID http://orcid.org/0009-0008-1106-3898
Pei-Shan WuDepartment of Microbiology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Miao-Hsia LinDepartment of Microbiology, National Taiwan University College of Medicine, Taipei City, Taiwan.
Li-Chung HsuInstitute of Molecular Medicine, National Taiwan University College of Medicine, Taipei City, Taiwan.ORCID http://orcid.org/0000-0001-7206-5231
Yen-Ling ChiuDepartment of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.ORCID http://orcid.org/0000-0003-4504-5571
Shih-Yu ChenTaiwan International Graduate Program in Molecular Medicine, National Yang Ming Chiao Tung University and Academia Sinica, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-7955-481X
Chong-Jen YuDepartment of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.ORCID http://orcid.org/0000-0001-5664-9392
Hsing-Chen TsaiGraduate Institute of Toxicology, National Taiwan University College of Medicine, Taipei City, Taiwan. htsai@ntu.edu.tw.ORCID http://orcid.org/0000-0002-7057-9084

Funding

Academia Sinica AS-TM-115-01-03National Taiwan University Hospital (NTUH) 115-SS0020National Taiwan University (NTU) 115L104309National Taiwan University (NTU) 115L892804
6 · The paper itself

Abstract

T cell exhaustion represents a critical target for immunotherapy in cancer. Nevertheless, T cells exhibit diminished responsiveness to immune checkpoint inhibitors once they transition to a terminally exhausted state. Here we used an epigenetic drug screen and identified bromodomain and extra-terminal motif inhibitors (BETis) as enhancers of effector functions in primary exhausted T cells (T

Indexed as

Epigenesis, GeneticLung NeoplasmsT-LymphocytesAnimalsHumansImmunotherapyMetabolic ReprogrammingMiceT-Cell Exhaustion

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.