Evidence map›Paper›PMID 40824199›Full record

ReviewCancer immunology research2025

A Dual Role for NKG7 in T-cell Cytotoxicity and Longevity.

Haidong Dong, Hyoungjun Ham, Whitney Barham, Ti Wen, Jacob B Hirdler, Zhiming Mao, Dallin S Ashton, Wenjing Zhang, Fabrice Lucien-Matteoni, Henrique Borges da Silva and 1 more

Abstract readReview
In one paragraph

Review in Cancer immunology research, 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. Article
  2. NR4A1 limits CD8Research square · 2026
    Article
  3. 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

11 authors.

Haidong DongDepartment of Urology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-5782-2983
Hyoungjun HamDepartment of Urology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-8669-6875
Whitney BarhamDepartment of Cancer Biology, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0002-1130-1971
Ti WenFirst hospital of China Medical University, Shenyang, China.ORCID 0000-0002-6688-211X
Jacob B HirdlerDepartment of Urology, Mayo Clinic, Rochester, Minnesota.ORCID 0009-0001-3674-0276
Zhiming MaoDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-7705-9575
Dallin S AshtonDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-2322-4862
Wenjing ZhangDepartment of Virology, Mayo Clinic, Rochester, Minnesota.ORCID 0009-0000-3523-1982
Fabrice Lucien-MatteoniDepartment of Urology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-6149-345X
Henrique Borges da SilvaDepartment of Immunology, Mayo Clinic, Phoenix, Arizona.ORCID 0000-0001-9424-3326
Daniel D BilladeauDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-2296-9547

Funding

Control of antiviral memory CD8+ T cell longevity by extracellular ATP sensingR01AI170649 · NIAID · MAYO CLINIC ARIZONA · PI Henrique Borges da Silva · 2022 to 2026
$2.4M
Center for Individualized Medicine, Mayo Clinic (CIM)Mayo Clinic Cancer CenterMayo Clinic Center for Biomedial DiscoveryNIAID NIH HHS R01 AI170649
6 · The paper itself

Abstract

The effectiveness of T cell-based immunotherapy depends on durable T-cell responses that can efficiently eliminate tumor cells. NKG7 was discovered three decades ago as a protein associated with lytic granules. However, only studies published over the past 5 years have contributed substantially to our understanding of NKG7 in T-cell biology. NKG7 has been recognized as an important T-cell functional marker in responses to immune checkpoint inhibitor therapy and in the prognosis of certain cancers. Besides its role in the generation, trafficking, and release of lytic granules, which is critical for efficient T-cell cytotoxicity against tumor cells, NKG7 has been identified as a key negative regulator of mTORC1 activity. By restraining mTORC1 activity, NKG7 promotes T-cell longevity and memory generation after infection. Importantly, NKG7 upregulation has demonstrated therapeutic potential in preclinical T-cell therapy for cancer. Collectively, NKG7 is emerging as a promising biomarker and therapeutic addition to T cell-based immunotherapies.

Indexed as

Cytotoxicity, ImmunologicNeoplasmsT-LymphocytesAnimalsHumans

Identifiers

PMID40824199
PMCPMC12485375

What OpenQuestion holds

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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.