Evidence map›Paper›PMID 9120387›Full record

ArticleThe Journal of experimental medicine1997

Regulation of the interleukin (IL)-12R beta 2 subunit expression in developing T helper 1 (Th1) and Th2 cells.

S J Szabo, A S Dighe, U Gubler, K M Murphy

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 270 papers.

0numbers the graph read from it
0cells of the map it votes in
270citing papers in PubMed
42.9field-weighted citation impact, top 1% 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

270 citing papers in PubMed, 1,004 citations in OpenAlex.

  1. Trial
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  7. A time-gated PKA-CREB signaling circuit licenses IL-12 responsiveness and Th1 fate in CD4Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Exploring Asthma as a Protective Factor in COVID-19 Outcomes.International journal of molecular sciences · 2025
    Review
  12. BALB/c mice infection with hybridFrontiers in cellular and infection microbiology · 2025
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Healthcare (Basel, Switzerland) · 2023
    Article
  18. Review
  19. Review
  20. Article

210 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

S J SzaboDepartment of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
A S Dighe
U Gubler
K M Murphy
Washington University in St. Louis · US

Funding

TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
THE ROLE OF T CELLS IN AUTOIMMUNE MYOCARDITISP01AI031238 · NIAID · WASHINGTON UNIVERSITY · PI UNANUE, EMIL RAPHAEL · 1991 to 2007
$6.4M
TRANSGENIC MOUSE MODEL OF HELPER T CELL DEVELOPMENT AND FUNCTIONU19AI034580 · NIAID · WASHINGTON UNIVERSITY · PI MURPHY, KENNETH M. · 1997 to 2000
$780k
TH1, TH2 CELLS IN INSULIN DEPENDENT DIABETES MELLITUSP01AI039676 · NIAID · WASHINGTON UNIVERSITY · PI KATZ, JONATHAN DAVID · 1996 to 1999
–
TRANSGENIC MOUSE MODEL OF HELPER T CELL DEVELOPMENT AND FUNCTIONU01AI034580 · NIAID · WASHINGTON UNIVERSITY · PI LUBLIN, D · 1993 to 1996
–
NCI NIH HHS T32 CA009547NIAID NIH HHS AI31238NIAID NIH HHS AI34580NIAID NIH HHS AI39676NIAID NIH HHS P01 AI031238
6 · The paper itself

Abstract

The developmental commitment to a T helper 1 (Th1)- or Th2-type response can significantly influence host immunity to pathogens. Extinction of the IL-12 signaling pathway during early Th2 development provides a mechanism that allows stable phenotype commitment. In this report we demonstrate that extinction of IL-12 signaling in early Th2 cells results from a selective loss of IL-12 receptor (IL-12R) beta 2 subunit expression. To determine the basis for this selective loss, we examined IL-12R beta 2 subunit expression during Th cell development in response to T cell treatment with different cytokines. IL-12R beta 2 is not expressed by naive resting CD4+ T cells, but is induced upon antigen activation through the T cell receptor. Importantly, IL-4 and IFN-gamma were found to significantly modify IL-12 receptor beta 2 expression after T cell activation. IL-4 inhibited IL-12R beta 2 expression leading to the loss of IL-12 signaling, providing an important point of regulation to promote commitment to the Th2 pathway. IFN-gamma treatment of early developing Th2 cells maintained IL-12R beta 2 expression and restored the ability of these cells to functionally respond to IL-12, but did not directly inhibit IL-4 or induce IFN-gamma production. Thus, IFN-gamma may prevent early Th cells from premature commitment to the Th2 pathway. Controlling the expression of the IL-12R beta 2 subunit could be an important therapeutic target for the redirection of ongoing Th cell responses.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationDNA-Binding ProteinsInterferon-gammaInterleukin-12MiceMice, Inbred BALB CMice, TransgenicProtein-Tyrosine KinasesReceptors, InterleukinReceptors, Interleukin-12RNA, MessengerSignal TransductionSpleenSTAT4 Transcription FactorDNA-Binding ProteinsInterferon-gammaInterleukin-12Protein-Tyrosine KinasesReceptors, InterleukinReceptors, Interleukin-12RNA, MessengerStat4 protein, mouseSTAT4 Transcription FactorTrans-Activators

Identifiers

PMID9120387
PMCPMC2196166
OpenAlexW2107860814

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.