Evidence map›Paper›PMID 21499227›Full record

ArticleThe EMBO journal2011

NFIL3/E4BP4 controls type 2 T helper cell cytokine expression.

Masaki Kashiwada, Suzanne L Cassel, John D Colgan, Paul B Rothman

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

53 citing papers in PubMed, 95 citations in OpenAlex.

  1. Trial
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  12. Zfp281 and Zfp148 control CD4Science immunology · 2023
    Article
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  14. Review
  15. Article
  16. Article
  17. Glucocorticoid circadian rhythms in immune function.Seminars in immunopathology · 2022
    Review
  18. Article
  19. Review
  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 1 institution in 1 country.

Masaki KashiwadaDepartment of Internal Medicine, University of Iowa, Iowa City, IA, USA.
Suzanne L Cassel
John D Colgan
Paul B Rothman
University of Iowa · US

Funding

IL-4 Signal TransductionR01AI054821 · NIAID · UNIVERSITY OF IOWA · PI COLGAN, JOHN D · 2003 to 2013
$3.6M
Regulation of Atopic Immune Responses by the Prolyl lsomerase Cyclophillin AR01AI067489 · NIAID · UNIVERSITY OF IOWA · PI COLGAN, JOHN D · 2006 to 2010
$1.8M
NIAID NIH HHS R01 AI054821NIAID NIH HHS R01 AI067489NIAID NIH HHS R01 AI54821
6 · The paper itself

Abstract

Type 2 T helper (T(H)2) cells are critical for the development of allergic immune responses; however, the molecular mechanism controlling their effector function is still largely unclear. Here, we report that the transcription factor NFIL3/E4BP4 regulates cytokine production and effector function by T(H)2 cells. NFIL3 is highly expressed in T(H)2 cells but much less in T(H)1 cells. Production of interleukin (IL)-13 and IL-5 is significantly increased in Nfil3(-/-) T(H)2 cells and is decreased by expression of NFIL3 in wild-type T(H)2 cells. NFIL3 directly binds to and negatively regulates the Il13 gene. In contrast, IL-4 production is decreased in Nfil3(-/-) T(H)2 cells. Increased IL-13 and IL-5 together with decreased IL-4 production by antigen-stimulated splenocytes from the immunized Nfil3(-/-) mice was also observed. The ability of NFIL3 to alter T(H)2 cytokine production is a T-cell intrinsic effect. Taken together, these data indicate that NFIL3 is a key regulator of T(H)2 responses.

Indexed as

Gene Expression RegulationAnimalsBasic-Leucine Zipper Transcription FactorsInterleukin-13Interleukin-4Interleukin-5MiceMice, Inbred C57BLMice, KnockoutTh2 CellsTranscription, GeneticBasic-Leucine Zipper Transcription FactorsInterleukin-13Interleukin-4Interleukin-5Nfil3 protein, mouse

Identifiers

PMID21499227
PMCPMC3098483
OpenAlexW1942080572

What OpenQuestion holds

Textmetadata
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.