Evidence map›Paper›PMID 25142300›Full record

ArticleEuropean journal of immunology2014

IL-15-dependent CD8+ CD122+ T cells ameliorate experimental autoimmune encephalomyelitis by modulating IL-17 production by CD4+ T cells.

Ping Yu, Richard N Bamford, Thomas A Waldmann

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

35 citing papers in PubMed, 43 citations in OpenAlex.

  1. CD8+ Regulatory T Cells.Annual review of immunology · 2026
    Review
  2. Acellular Pertussis Vaccines Induce CD8European journal of immunology · 2025
    Article
  3. Article
  4. An angel or a devil? Current view on the role of CD8Journal of translational medicine · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. A Functionally Distinct CXCR3Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  10. Review
  11. CD8Frontiers in immunology · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. CD8+CD103+ iTregs Inhibit Chronic Graft-versus-Host Disease with Lupus Nephritis by the Increased Expression of CD39.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  18. Future prospects for CD8Immunological reviews · 2019
    Review
  19. Article
  20. Regulatory T cells limit unconventional memory to preserve the capacity to mount protective CD8 memory responses to pathogens.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

3 authors at 3 institutions in 1 country.

Ping YuLymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Richard N Bamford
Thomas A Waldmann
Aptagen (United States) · USCenter for Cancer Research · USNational Cancer Institute · US

Funding

IL-2:IL-15 : implications for cancer therapy (Investigator -Initiated Project)ZIASC004002 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WALDMANN, THOMAS · 2009 to 2022
$22.9M
Intramural NIH HHS ZIA SC004002
6 · The paper itself

Abstract

Interleukin-15 (IL-15) is an inflammatory cytokine whose role in autoimmune diseases has not been fully elucidated. Th17 cells have been shown to play critical roles in experimental autoimmune encephalomyelitis (EAE) models. In this study, we demonstrate that blockade of IL-15 signaling by TMβ-1 mAb treatment aggravated EAE severity. The key mechanism was not NK-cell depletion but depletion of CD8+ CD122+ T cells. Adoptive transfer of exogenous CD8+ CD122+ T cells to TMβ-1-treated mice rescued animals from severe disease. Moreover, transfer of preactivated CD8+ CD122+ T cells prevented EAE development and significantly reduced IL-17 secretion. Naïve effector CD4+ CD25- T cells cultured with either CD8+ CD122+ T cells from wild-type mice or IL-15 transgenic mice displayed lower frequencies of IL-17A production with lower amounts of IL-17 in the supernatants when compared with production by effector CD4+ CD25- T cells cultured alone. Addition of a neutralizing antibody to IL-10 led to recovery of IL-17A production in Th17 cultures. Furthermore, coculture of CD8+ CD122+ T cells with effector CD4+ T cells inhibited their proliferation significantly, suggesting a regulatory function for IL-15 dependent CD8+ CD122+ T cells. Taken together, these observations suggest that IL-15, acting through CD8+ CD122+ T cells, has a negative regulatory role in reducing IL-17 production and Th17-mediated EAE inflammation.

Indexed as

Adoptive TransferAnimalsAntibodies, MonoclonalAntibodies, NeutralizingCD8-Positive T-LymphocytesCell DifferentiationCell ProliferationCells, CulturedCoculture TechniquesEncephalomyelitis, Autoimmune, ExperimentalInterleukin-15Interleukin-17Interleukin-2 Receptor beta SubunitKiller Cells, NaturalLymphocyte ActivationLymphocyte DepletionAntibodies, MonoclonalAntibodies, NeutralizingIl17a protein, mouseIl2rb protein, mouseInterleukin-15Interleukin-17Interleukin-2 Receptor beta SubunitCD8+CD122+ T cellsExperimental autoimmune encephalomyelitisInterleukin-15Interleukin-17Multiple sclerosis

Identifiers

PMID25142300
PMCPMC7720079
OpenAlexW1581633343

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.