Evidence map›Paper›PMID 36681605›Full record

ReviewTrends in cancer2023

T cell exhaustion in malignant gliomas.

Matthew B Watowich, Mark R Gilbert, Mioara Larion

Open access · hybridAbstract readReview
In one paragraph

Review in Trends in cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 1 pooled it
36.2field-weighted citation impact, top 1% of its field
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

90 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Pooled it
  2. Oncoimmunology · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. All-trans retinoic acid suppresses CD8Signal transduction and targeted therapy · 2026
    Article
  7. Immunotherapy for Glioma: A compartmental framework for resistance and rational combination design.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  8. Decoding IGLL5 Mutation-Mediated BCR Signaling: A Novel Mechanism of CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Spatiotemporal cancer controlNanomedicine (London, England) · 2026
    Review
  18. Article
  19. Article
  20. Article

30 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Matthew B WatowichNeuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Mark R GilbertNeuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Mioara LarionNeuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: mioara.larion@nih.gov.
National Institutes of Health · US

Funding

Translational ImmunologyZIABC011714 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GILBERT, MARK · 2016 to 2024
$4.0M
Develop RAMAN imaging to visualize metabolism in cell lines and tissueZIABC011711 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARION, MIOARA · 2016 to 2025
$3.3M
The effect of therapeutics on mutated IDH1 cell lines and mice tumor modelsZIABC011707 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARION, MIOARA · 2016 to 2025
$2.4M
Targeted and untargeted metabolomics in IDH1 mutated xenografts in miceZIABC011708 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARION, MIOARA · 2016 to 2025
$2.4M
In vivo and in vitro metabolic flux analysis in preclinical mouse modelsZIABC011710 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARION, MIOARA · 2016 to 2025
$2.4M
Metabolite profiling of patients blood, urine, cerebrospinal fluid and tissueZIABC011709 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARION, MIOARA · 2016 to 2025
$1.6M
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC011707Intramural NIH HHS ZIA BC011708Intramural NIH HHS ZIA BC011709Intramural NIH HHS ZIA BC011710Intramural NIH HHS ZIA BC011711
6 · The paper itself

Abstract

Despite advances in understanding tumor biology, malignant gliomas remain incurable. While immunotherapy has improved outcomes in other cancer types, comparable efficacy has not yet been demonstrated for primary cancers of the central nervous system (CNS). T cell exhaustion, defined as a progressive decrease in effector function, sustained expression of inhibitory receptors, metabolic dysfunction, and distinct epigenetic and transcriptional alterations, contributes to the failure of immunotherapy in the CNS. Herein, we describe recent advances in understanding the drivers of T cell exhaustion in the glioma microenvironment. We discuss the extrinsic and intrinsic factors that contribute to exhaustion and highlight potential avenues for reversing this phenotype. Our ability to directly target specific immunosuppressive drivers in brain cancers would be a major advance in immunotherapy.

Indexed as

Brain NeoplasmsGliomaCentral Nervous SystemHumansImmunotherapyT-Cell ExhaustionTumor Microenvironmentexhaustionimmunologyneuro-oncologyT cellstreatment modalities

Identifiers

PMID36681605
PMCPMC10038906
OpenAlexW4317708616

What OpenQuestion holds

Textmetadata
LicenceTDM
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.