Evidence map›Paper›PMID 20080304›Full record

ArticleMolecular immunology2010

Regulation of IL-17 expression by the developmental pathway of CD4 T cells in the thymus.

M Hanief Sofi, Zhiping Liu, Lingqiao Zhu, Qiao Yu, Mark H Kaplan, Cheong-Hee Chang

Abstract read
In one paragraph

Article in Molecular immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. The circadian gene Arntl2 on distal mouse chromosome 6 controls thymocyte apoptosis.Mammalian genome : official journal of the International Mammalian Genome Society · 2017
    Article
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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

6 authors at 2 institutions in 1 country.

M Hanief SofiDepartment of Microbiology and Immunology, The University of Michigan Medical School, Ann Arbor, MI 48109-0620, USA.
Zhiping Liu
Lingqiao Zhu
Qiao Yu
Mark H Kaplan
Cheong-Hee Chang
University of Michigan–Ann Arbor · USIndiana University – Purdue University Indianapolis · US

Funding

Immune regulation by thymocyte-selected CD4 T cellsR01AI073677 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHANG, CHEONG-HEE · 2009 to 2013
$1.6M
NIAID NIH HHS R01 AI073677
6 · The paper itself

Abstract

CD4 T cells selected by MHC class II expressing thymocytes (T-CD4 T cells) have distinct effector functions compared to that of epithelial cell-selected CD4 T cells (E-CD4 T cells). T-CD4 T cells produce both Th1 and Th2 effector cytokines immediately after stimulation and also express IL-4 in addition to IFN-gamma under the Th1 differentiation condition. In the present study, we investigated the capability of T-CD4 T cells to become IL-17-producing cells. We found that T-CD4 T cells express reduced IL-17 under Th17-inducing conditions. T-CD4 T cells express very low levels of receptor for TGF-beta and IL-21 that are essential to induce IL-17 expression. In addition, the induction of RORgammat, a key transcription factor for IL-17 gene expression, was compromised in T-CD4 T cells under Th17 skewing conditions and ectopic expression of RORgammat restored IL-17 expression. The defect of IL-17 and RORgammat expression in T-CD4 T cells is cell intrinsic and not due to effects of a secreted factor. Thus, the developmental pathway of CD4 T cells in the thymus plays a critical role in controlling an immune response by suppressing the generation of the Th17 lineage.

Indexed as

Gene Expression RegulationAnimalsCD4-Positive T-LymphocytesCell SeparationHumansInterleukin-17Interleukin-4MiceMice, TransgenicNuclear ProteinsNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Interleukin-21Receptors, Transforming Growth Factor betaSTAT6 Transcription FactorThymus GlandTrans-ActivatorsInterleukin-17Interleukin-4MHC class II transactivator proteinNuclear ProteinsNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Interleukin-21Receptors, Transforming Growth Factor betaStat6 protein, mouseSTAT6 Transcription FactorTrans-Activators

Identifiers

PMID20080304
PMCPMC2830291
OpenAlexW2075878311

What OpenQuestion holds

Textmetadata
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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.