Evidence map›Paper›PMID 10209051›Full record

ArticleThe Journal of experimental medicine1999

Lineage-specific requirement for signal transducer and activator of transcription (Stat)4 in interferon gamma production from CD4(+) versus CD8(+) T cells.

L L Carter, K M Murphy

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 168 citations in OpenAlex.

  1. Review
  2. Article
  3. The expanding Pandora's toolbox of CD8Journal of translational medicine · 2023
    Review
  4. Article
  5. Article
  6. Dynamic Roles for IL-2-STAT5 Signaling in Effector and Regulatory CD4Journal of immunology (Baltimore, Md. : 1950) · 2020
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. T cell responses in the central nervous system.Nature reviews. Immunology · 2017
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  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

2 authors at 1 institution in 1 country.

L L CarterDepartment of Pathology and Center for Immunology, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
K M Murphy
Howard Hughes Medical Institute · US

Funding

TRANSGENIC MOUSE MODEL OF HELPER T CELL DEVELOPMENT AND FUNCTIONU19AI034580 · NIAID · WASHINGTON UNIVERSITY · PI CHAPLIN, DAVID D · 1997 to 2000
$780k
TH1, TH2 CELLS IN INSULIN DEPENDENT DIABETES MELLITUSP01AI039676 · NIAID · WASHINGTON UNIVERSITY · PI UNANUE, EMIL R · 1996 to 1999
–
TRANSGENIC MOUSE MODEL OF HELPER T CELL DEVELOPMENT AND FUNCTIONU01AI034580 · NIAID · WASHINGTON UNIVERSITY · PI WEDNER, H J · 1993 to 1996
–
NIAID NIH HHS AI34580NIAID NIH HHS AIDK39676PHS HHS JDF995012
6 · The paper itself

Abstract

CD4(+) and CD8(+) T cells exhibit important differences in their major effector functions. CD8(+) T cells provide protection against pathogens through cytolytic activity, whereas CD4(+) T cells exert important regulatory activity through production of cytokines. However, both lineages can produce interferon (IFN)-gamma, which can contribute to protective immunity. Here we show that CD4(+) and CD8(+) T cells differ in their regulation of IFN-gamma production. Both lineages require signal transducer and activator of transcription (Stat)4 activation for IFN-gamma induced by interleukin (IL)-12/IL-18 signaling, but only CD4(+) T cells require Stat4 for IFN-gamma induction via the TCR pathway. In response to antigen, CD8(+) T cells can produce IFN-gamma independently of IL-12, whereas CD4(+) T cells require IL-12 and Stat4 activation. Thus, there is a lineage-specific requirement for Stat4 activation in antigen-induced IFN-gamma production based on differences in TCR signaling between CD4(+) and CD8(+) T cells.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDNA-Binding ProteinsFlow CytometryInterferon-gammaInterleukin-12Interleukin-18MiceMice, TransgenicReceptors, Antigen, T-CellSignal TransductionSTAT4 Transcription FactorTrans-ActivatorsDNA-Binding ProteinsInterferon-gammaInterleukin-12Interleukin-18Receptors, Antigen, T-CellStat4 protein, mouseSTAT4 Transcription FactorTrans-Activators

Identifiers

PMID10209051
PMCPMC2193026
OpenAlexW2152729998

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.