Evidence map›Paper›PMID 22078635›Full record

ArticleCytokine2012

IL-4 acts as a potent stimulator of IFN-γ expression in CD8+ T cells through STAT6-dependent and independent induction of Eomesodermin and T-bet.

Jennifer A Oliver, Valerie R Stolberg, Stephen W Chensue, Philip D King

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Cytokine-Based Generation of CD49aFrontiers in immunology · 2018
    Article
  11. Article
  12. Review
  13. Innate memory T cells.Advances in immunology · 2015
    Review
  14. Article
  15. Article
  16. Article
  17. Increased peripheral IL-4 leads to an expanded virtual memory CD8+ population.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Article
  18. Review
  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

4 authors at 2 institutions in 1 country.

Jennifer A OliverDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109-5620, USA.
Valerie R Stolberg
Stephen W Chensue
Philip D King
University of Michigan–Ann Arbor · USVA Ann Arbor Healthcare System · US

Funding

Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
Control of T cell activation by the TSAd adapter proteinR01AI050699 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KING, PHILIP D · 2002 to 2006
$1.4M
NIAID NIH HHS AI050699NIAID NIH HHS R01 AI050699NIGMS NIH HHS T32 GM145304
6 · The paper itself

Abstract

CD8+ T cell synthesis of IFN-γ is an important component of the CD8+ T cell immune response. In short-term cultures of murine pan-T cells, we found that IL-4 was the principal cytokine responsible for driving IFN-γ synthesis by CD3/CD28-activated CD8+ T cells. IL-4 was able to induce low levels of IFN-γ mRNA in CD8+ T cells even in the absence of CD3/CD28 engagement, although concomitant CD3/CD28 stimulation was necessary for IFN-γ secretion. IL-4 induction of IFN-γ was explained by its ability to induce Eomesodermin and T-bet transcription factors whose expression was further increased by CD3/CD28. Expression of Eomesodermin, T-bet and IFN-γ induced by IL-4 was partially dependent upon activation of MAPK and PI3K but independent of the canonical IL-4-activated transcription factor, STAT6. In contrast, expression of IFN-γ induced by IL-4/CD3/CD28 stimulation showed additional dependency upon STAT6 which functions to increase expression of Eomesodermin specifically. These novel findings point to a function for IL-4 as a direct regulator of IFN-γ expression in CD8+ T cells and reveal the molecular mechanisms involved.

Indexed as

AnimalsAntibodies, MonoclonalCD28 AntigensCD3 ComplexCD8-Positive T-LymphocytesCell ProliferationCytotoxicity, ImmunologicEnzyme ActivationInterferon-gammaInterleukin-2Interleukin-4Intracellular SpaceMiceMice, Inbred C57BLMitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesAntibodies, MonoclonalCD28 AntigensCD3 ComplexEomes protein, mouseInterferon-gammaInterleukin-2Interleukin-4Mitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesReceptors, Antigen, T-CellStat6 protein, mouseSTAT6 Transcription FactorT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID22078635
PMCPMC3246089
OpenAlexW1973473486

What OpenQuestion holds

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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.