Evidence map›Paper›PMID 1569401›Full record

ArticleThe Journal of experimental medicine1992

Differential induction of transcription factors that regulate the interleukin 2 gene during anergy induction and restimulation.

C Go, J Miller

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1992. 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
5.2field-weighted citation impact, top 4% 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, 63 citations in OpenAlex.

  1. Article
  2. Biochemical features of anergic T cells.Immunologic research · 1998
    Review
  3. Article
  4. Review
  5. In vivo anergized CD4+ T cells express perturbed AP-1 and NF-kappa B transcription factors.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  6. Article
  7. Article
  8. Negative transcriptional regulation in anergic T cells.Proceedings of the National Academy of Sciences of the United States of America · 1995
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Expression and functional significance of an additional ligand for CTLA-4.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
  15. Article
  16. Article
  17. Article
  18. Molecular regulation of human interleukin 2 and T-cell function by interleukin 4.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
  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.

C GoDepartment of Pathology, University of Chicago, Illinois 60637.
J Miller
University of Illinois Chicago · US

Funding

MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
PANCREATIC ISLET ANTIGENS--TOLERANCE AND AUTOIMMUNITYR01DK042857 · NIDDK · UNIVERSITY OF CHICAGO · PI MILLER, JIM F · 1991 to 1993
–
ROLE OF INTRACELLULAR IA IN ANTIGEN PRESENTATIONR01GM042071 · NIGMS · UNIVERSITY OF CHICAGO · PI MILLER, JIM F · 1988 to 1999
–
NIDDK NIH HHS DK-42857NIGMS NIH HHS GM-42071NIGMS NIH HHS PHS-GM-07281
6 · The paper itself

Abstract

T cell activation requires two distinct signals. The first is delivered through the antigen-specific T cell receptor (TCR), and the second is provided by costimulatory molecule(s) present on the surface of the antigen-presenting cell (APC). Stimulation of T helper type 1 T cell clones through the TCR in the absence of the costimulatory activity results in a lack of interleukin 2 (IL-2) secretion and proliferation, and the induction of a long-lived state of nonresponsiveness, termed anergy. In this study, we have examined the transcription factors involved in IL-2 gene expression that are expressed after stimulation of normal T cell clones through the TCR with and without engagement of the necessary costimulatory molecule(s). Antigen-specific activation of the clones results in the induction of a similar pattern of transcription factors that have been previously shown to regulate IL-2 expression. In contrast, antigen presentation by chemically fixed APC, a condition that results in T cell anergy, induces neither NF-AT nor one of the two NF-kappa B binding factors. Thus, the failure to express IL-2 during the induction of T cell anergy may be attributed to the absence of these two transcription factors. When anergized T cells are restimulated with antigen and conventional APC, they induce the transcription factors associated with IL-2 expression, but they fail to synthesize measurable IL-2. Taken together, these data indicate that the control of IL-2 gene expression during anergy induction and during normal stimulation of anergized cells are distinct, and suggest the presence of additional regulatory elements in the IL-2 gene.

Indexed as

Gene Expression RegulationAnimalsCell DivisionInterleukin-2KineticsMiceMice, Inbred BALB CNF-kappa BProto-Oncogene Proteins c-junReceptors, Antigen, T-CellT-LymphocytesTranscription FactorsUp-RegulationInterleukin-2NF-kappa BProto-Oncogene Proteins c-junReceptors, Antigen, T-CellTranscription Factors

Identifiers

PMID1569401
PMCPMC2119197
OpenAlexW2164062179

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.