Evidence map›Paper›PMID 38053333›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

Soluble CTLA-4 attenuates T cell activation and modulates anti-tumor immunity.

Paul T Kennedy, Emma L Saulters, Andrew D Duckworth, Yeong Jer Lim, John F Woolley, Joseph R Slupsky, Mark S Cragg, Frank J Ward, Lekh N Dahal

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
11.3field-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

40 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Splicing-driven post-translational dysregulation: a new frontier for precision cancer medicine and immunotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  6. Review
  7. Role of alternative splicing in cancer progression.Irish journal of medical science · 2026
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Proteostasis of immune checkpoint receptors.The Biochemical journal · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Paul T KennedyDepartment of Pharmacology and Therapeutics, University of Liverpool, L69 3GE Liverpool, UK.
Emma L SaultersDepartment of Pharmacology and Therapeutics, University of Liverpool, L69 3GE Liverpool, UK.
Andrew D DuckworthDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, L69 3GE Liverpool, UK.
Yeong Jer LimDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, L69 3GE Liverpool, UK.
John F WoolleyDepartment of Pharmacology and Therapeutics, University of Liverpool, L69 3GE Liverpool, UK.
Joseph R SlupskyDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, L69 3GE Liverpool, UK.
Mark S CraggCentre for Cancer Immunology, University of Southampton, SO16 6YD Southampton, UK.
Frank J WardDepartment of Immunology, University of Aberdeen, AB25 2ZD Aberdeen, UK.
Lekh N DahalDepartment of Pharmacology and Therapeutics, University of Liverpool, L69 3GE Liverpool, UK. Electronic address: l.n.dahal@liverpool.ac.uk.
University of Liverpool · GBUniversity of Aberdeen · GBUniversity of Southampton · GB

Funding

Cancer Research UK 20537
6 · The paper itself

Abstract

CTLA-4 is a crucial immune checkpoint receptor involved in the maintenance of immune homeostasis, tolerance, and tumor control. Antibodies targeting CTLA-4 have been promising treatments for numerous cancers, but the mechanistic basis of their anti-tumoral immune-boosting effects is poorly understood. Although the ctla4 gene also encodes an alternatively spliced soluble variant (sCTLA-4), preclinical/clinical evaluation of anti-CTLA-4-based immunotherapies have not considered the contribution of this isoform. Here, we explore the functional properties of sCTLA-4 and evaluate the efficacy of isoform-specific anti-sCTLA-4 antibody targeting in a murine cancer model. We show that expression of sCTLA-4 by tumor cells suppresses CD8

Indexed as

CD8-Positive T-LymphocytesNeoplasmsAnimalsAntibodiesCTLA-4 AntigenMiceProtein IsoformsAntibodiesCTLA-4 AntigenCtla4 protein, mouseProtein Isoformscancerimmune checkpointimmune regulationimmunomodulationimmunotherapysoluble CTLA-4

Identifiers

PMID38053333
PMCPMC10861965
OpenAlexW4389346485

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.