Evidence map›Paper›PMID 24470500›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

IL-21 promotes CD4 T cell responses by phosphatidylinositol 3-kinase-dependent upregulation of CD86 on B cells.

Kesley Attridge, Rupert Kenefeck, Lukasz Wardzinski, Omar S Qureshi, Chun Jing Wang, Claire Manzotti, Klaus Okkenhaug, Lucy S K Walker

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. GPR174 signals via GProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. PI3K Isoforms in B Cells.Current topics in microbiology and immunology · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Germline-activating mutations inThe Journal of experimental medicine · 2018
    Article
  19. Review
  20. Synaptic Interactions in Germinal Centers.Frontiers in immunology · 2018
    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

8 authors at 4 institutions in 1 country.

Kesley AttridgeMedical Research Council Centre for Immune Regulation, University of Birmingham Medical School, Birmingham B15 2TT, United Kingdom;
Rupert Kenefeck
Lukasz Wardzinski
Omar S Qureshi
Chun Jing Wang
Claire Manzotti
Klaus Okkenhaug
Lucy S K Walker
Medical Research Council · GBUniversity College London · GBBabraham Institute · GBUniversity of Birmingham · GB

Funding

Biotechnology and Biological Sciences Research Council BB/E009867/1Biotechnology and Biological Sciences Research Council BB/E010016/1Medical Research Council G0802382Wellcome Trust 085896
6 · The paper itself

Abstract

The cytokine IL-21 is a potent immune modulator with diverse mechanisms of action on multiple cell types. IL-21 is in clinical use to promote tumor rejection and is an emerging target for neutralization in the setting of autoimmunity. Despite its clinical potential, the biological actions of IL-21 are not yet fully understood and the full range of effects of this pleiotropic cytokine are still being uncovered. In this study, we identify a novel role for IL-21 as an inducer of the costimulatory ligand CD86 on B lymphocytes. CD86 provides critical signals through T cell-expressed CD28 that promote T cell activation in response to Ag engagement. Expression levels of CD86 are tightly regulated in vivo, being actively decreased by regulatory T cells and increased in response to pathogen-derived signals. In this study, we demonstrate that IL-21 can trigger potent and sustained CD86 upregulation through a STAT3 and PI3K-dependent mechanism. We show that elevated CD86 expression has functional consequences for the magnitude of CD4 T cell responses both in vitro and in vivo. These data pinpoint CD86 upregulation as an additional mechanism by which IL-21 can elicit immunomodulatory effects.

Indexed as

AnimalsB7-2 AntigenB-LymphocytesInterleukin-21InterleukinsMiceMice, Inbred BALB CMice, KnockoutPhosphatidylinositol 3-KinasesSTAT3 Transcription FactorT-Lymphocytes, RegulatoryUp-RegulationB7-2 AntigenCd86 protein, mouseInterleukin-21InterleukinsPhosphatidylinositol 3-KinasesStat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID24470500
PMCPMC3932810
OpenAlexW2110471797

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.