Evidence map›Paper›PMID 31107985›Full record

ReviewImmunology2019

Phosphoinositide 3-kinase δ is a regulatory T-cell target in cancer immunotherapy.

Ee Lyn Lim, Klaus Okkenhaug

Open access · bronzeAbstract readReview
In one paragraph

Review in Immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Targeting T regulatory (TCancer drug resistance (Alhambra, Calif.) · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. PI3K inhibitors are finally coming of age.Nature reviews. Drug discovery · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 2 institutions in 2 countries.

Ee Lyn LimLaboratory of Experimental Immunology, Immunology Frontier Research Centre, Osaka University, Suita, Japan.ORCID 0000-0002-5173-2979
Klaus OkkenhaugDivision of Immunology, Department of Pathology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-9432-4051
The University of Osaka · JPUniversity of Cambridge · GB

Funding

Wellcome TrustWellcome Trust 095691/Z/11/Z
6 · The paper itself

Abstract

Tumour infiltration by regulatory T (Treg) cells contributes to suppression of the anti-tumour immune response, which limits the efficacy of immune-mediated cancer therapies. The phosphoinositide 3-kinase (PI3K) pathway has key roles in mediating the function of many immune cell subsets, including Treg cells. Treg function is context-dependent and depends on input from different cell surface receptors, many of which can activate the PI3K pathway. In this review, we explore how PI3Kδ contributes to signalling through several major immune cell receptors, including the T-cell receptor and co-stimulatory receptors such as CD28 and ICOS, but is antagonized by the immune checkpoint receptors CTLA-4 and PD-1. Understanding how PI3Kδ inhibition affects Treg signalling events will help to inform how best to use PI3Kδ inhibitors in clinical cancer treatment.

Indexed as

ImmunotherapyAnimalsAntineoplastic AgentsClass Ib Phosphatidylinositol 3-KinaseHumansLymphocytes, Tumor-InfiltratingMolecular Targeted TherapyNeoplasmsPhenotypeProtein Kinase InhibitorsSignal TransductionT-Lymphocytes, RegulatoryTumor EscapeTumor MicroenvironmentAntineoplastic AgentsClass Ib Phosphatidylinositol 3-KinasePIK3CG protein, humanProtein Kinase Inhibitorsregulatory T cellsignal transductionT celltumour immunology

Identifiers

PMID31107985
PMCPMC6587315
OpenAlexW2944827335

What OpenQuestion holds

Textmetadata
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.