Evidence map›Paper›PMID 40330479›Full record

ReviewFrontiers in immunology2025

From

Morgane Chauvet, Dorothée Bourges, Emmanuel Scotet

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Morgane ChauvetNantes Université, Inserm UMR 1307, CNRS UMR 6075, Université d'AngersCRCI2NA, Nantes, France.
Dorothée BourgesSanofi, Oncology, Vitry-sur-Seine, France.
Emmanuel ScotetNantes Université, Inserm UMR 1307, CNRS UMR 6075, Université d'AngersCRCI2NA, Nantes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human γδ T cells demonstrate remarkable and diverse antitumor properties driven by TCR-dependent activation. Their non-alloreactive nature and pivotal role in cancer immunity position them as attractive targets for immunotherapies. However, upon infiltrating tumors, due to mechanisms induced by the tumor microenvironment's immune evasion strategies, these cells frequently become exhausted, greatly weakening the efficacy and antitumor potential of novel immunotherapeutic treatments. While being extensively characterized in CD8

Indexed as

ImmunotherapyNeoplasmsReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsAnimalsDisease Models, AnimalHumansLymphocyte ActivationMiceTumor MicroenvironmentReceptors, Antigen, T-Cell, gamma-deltacancerimmunotherapyin vitro modelsT cell exhaustionVγ9Vδ2 T cell

Identifiers

PMID40330479
PMCPMC12052970

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.