Evidence map›Paper›PMID 26311905›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

PI3Kδ Regulates the Magnitude of CD8+ T Cell Responses after Challenge with Listeria monocytogenes.

Verity Q Pearce, Hicham Bouabe, Amy R MacQueen, Valentina Carbonaro, Klaus Okkenhaug

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03698383 (Phase II Study of Trastuzumab Biosimilar), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 12% 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.

NCT03698383 phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Phase II Study of Trastuzumab Biosimilar (Herzuma®) Plus Gedatolisib in Patients With HER-2 Positive Metastatic Breast Cancer Who Progressed After 2 or More HER-2 Directed Chemotherapy

TypeinterventionalSponsorKorean Cancer Study GroupRan2019 to 2021Enrolled15ConditionsHER2-positive Breast Cancer, Metastatic Breast CancerArmsTrastuzumab biosimilars(Herzuma), Gedatolisib
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. CD4Frontiers in immunology · 2025
    Review
  5. PI3K Isoforms in CD8Current topics in microbiology and immunology · 2022
    Article
  6. Article
  7. PI3K in T Cell Adhesion and Trafficking.Frontiers in immunology · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Exhaustion of the CD8Frontiers in immunology · 2018
    Article
  20. 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

5 authors at 1 institution in 1 country.

Verity Q PearceLaboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge CB22 3AT, United Kingdom.
Hicham BouabeLaboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge CB22 3AT, United Kingdom.
Amy R MacQueenLaboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge CB22 3AT, United Kingdom.
Valentina CarbonaroLaboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge CB22 3AT, United Kingdom.
Klaus OkkenhaugLaboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge CB22 3AT, United Kingdom klaus.okkenhaug@babraham.ac.uk.ORCID http://orcid.org/0000-0002-9432-4051
Babraham Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F015461/1Biotechnology and Biological Sciences Research Council BBS/E/B/0000L225Biotechnology and Biological Sciences Research Council BBS/E/B/0000L734Biotechnology and Biological Sciences Research Council BBS/E/B/000C0407Biotechnology and Biological Sciences Research Council BBS/E/B/000C0409Wellcome Trust 095691
6 · The paper itself

Abstract

PI3Ks regulate diverse immune cell functions by transmitting intracellular signals from Ag, costimulatory receptors, and cytokine receptors to control cell division, differentiation, survival, and migration. In this study, we report the effect of inhibiting the p110δ subunit of PI3Kδ on CD8(+) T cell responses to infection with the intracellular bacteria Listeria monocytogenes. A strong dependency on PI3Kδ for IFN-γ production by CD8(+) T cells in vitro was not recapitulated after Listeria infection in vivo. Inactivation of PI3Kδ resulted in enhanced bacterial elimination by the innate immune system. However, the magnitudes of the primary and secondary CD8 +: T cell responses were reduced. Moreover, PI3Kδ activity was required for CD8(+) T cells to provide help to other responding CD8(+) cells. These findings identify PI3Kδ as a key regulator of CD8(+) T cell responses that integrates extrinsic cues, including those from other responding cells, to determine the collective behavior of CD8(+) T cell populations responding to infection.

Indexed as

Phosphoinositide-3 Kinase InhibitorsAdoptive TransferAnimalsCD8-Positive T-LymphocytesClass I Phosphatidylinositol 3-KinasesCytokinesGranzymesImmunologic MemoryImmunosenescenceInterferon-gammaListeria monocytogenesListeriosisMiceMice, Inbred C57BLMice, TransgenicPhosphatidylinositol 3-KinasesClass I Phosphatidylinositol 3-KinasesCytokinesGranzymesGzmb protein, mouseInterferon-gammaPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPik3cd protein, mouseProto-Oncogene Proteins c-akt

Identifiers

PMID26311905
PMCPMC4574522
OpenAlexW1914351900

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.