Evidence map›Paper›PMID 39430319›Full record

ArticleTranslational lung cancer research2024

Stem-like exhausted CD8 T cells in pleural effusions predict improved survival in non-small cell lung cancer (NSCLC) and mesothelioma.

Linda Ye, Heeju Ryu, David Granadier, Long T Nguyen, Yannick Simoni, Ian Dick, Tina Firth, Ebony Rouse, Peter Chiang, Y C Gary Lee and 4 more

Abstract read
In one paragraph

Article in Translational lung cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Terminally exhausted CD8Frontiers in immunology · 2025
    Review
  9. Review
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

14 authors.

Linda Ye *National Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.
Heeju Ryu *Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Centre, Seattle, WA, USA.
David GranadierVaccine and Infectious Disease Division, Fred Hutchinson Cancer Centre, Seattle, WA, USA.
Long T NguyenVaccine and Infectious Disease Division, Fred Hutchinson Cancer Centre, Seattle, WA, USA.
Yannick SimoniVaccine and Infectious Disease Division, Fred Hutchinson Cancer Centre, Seattle, WA, USA.
Ian DickSchool of Biomedical Science, University of Western Australia, Nedlands, WA, Australia.
Tina FirthNational Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.
Ebony RouseNational Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.
Peter ChiangNational Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.
Y C Gary LeeSchool of Biomedical Science, University of Western Australia, Nedlands, WA, Australia.
Bruce W RobinsonNational Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.
Jenette CreaneyNational Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.
Evan W Newell *Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Centre, Seattle, WA, USA.
Alec J Redwood *National Centre for Asbestos Related Diseases, Faculty of Health and Medical Science, University of Western Australia, Nedlands, WA, Australia.

Funding

Deeply analyzing MHC class I-restricted peptide presentation mechanistics across alleles, pathways, and disease coupled with TCR discovery/characterizationR01AI176563 · NIAID · FRED HUTCHINSON CANCER CENTER · PI Roland K Strong · 2023 to 2026
$3.2M
The roles of EBV-specific T cells in response to checkpoint blockade immunotherapy of EBV-driven nasopharyngeal carcinomaR01CA264646 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWELL, EVAN · 2021 to 2025
$3.0M
NCI NIH HHS R01 CA264646NIAID NIH HHS R01 AI176563
6 · The paper itself

Abstract

Background: Anti-tumor CD8 T cells are important for immunity but can become 'exhausted' and hence ineffective. Tumor-infiltrating exhausted CD8 Methods: Pre-treatment malignant pleural effusions (PEs) from 43 NSCLC (41 non-squamous, 2 squamous) patients were analyzed by flow cytometry. The percentages of Tex Results: Higher frequency of Tex Conclusions: This study demonstrates that PE CD8 Tex

Indexed as

mesotheliomaNon-small cell lung cancer (NSCLC)T cell exhaustion

Identifiers

PMID39430319
PMCPMC11484714

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.