Evidence map›Paper›PMID 18164222›Full record

ArticleImmunity2008

T helper 17 lineage differentiation is programmed by orphan nuclear receptors ROR alpha and ROR gamma.

Xuexian O Yang, Bhanu P Pappu, Roza Nurieva, Askar Akimzhanov, Hong Soon Kang, Yeonseok Chung, Li Ma, Bhavin Shah, Athanasia D Panopoulos, Kimberly S Schluns and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 855 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
855citing papers in PubMed, 2 pooled it
52.3field-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

855 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,586 citations in OpenAlex.

  1. Interleukin-17A mRNA Expression is Associated with the Prognosis of Patients with Colorectal Cancer: A Pooled Meta-Analysis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2022
    Pooled it
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  17. Frontiers in immunology · 2026
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795 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 2 countries.

Xuexian O YangDepartment of Immunology, M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Bhanu P Pappu
Roza Nurieva
Askar Akimzhanov
Hong Soon Kang
Yeonseok Chung
Li Ma
Bhavin Shah
Athanasia D Panopoulos
Kimberly S Schluns
Stephanie S Watowich
Qiang Tian
Anton M Jetten
Chen Dong
Institute for Systems Biology · USInSysBio (Russia) · RUNational Institutes of Health · USThe University of Texas MD Anderson Cancer Center · USTriangle · US

Funding

Nuclear receptors: action, functions, and roles in diseaseZIAES101586 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI JETTEN, ANTON M · 2009 to 2025
$13.5M
TSLP Signaling in Dendritic Cells - Aim 3U19AI071130 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ZIEGLER, STEVEN F · 2006 to 2010
$6.1M
Transcriptional regulation of inflammatory helper T Cell differentiationR01AR050772 · NIAMS · UNIVERSITY OF WASHINGTON · PI DONG, CHEN · 2003 to 2016
$4.5M
NIAID NIH HHS U19 AI071130NIAMS NIH HHS AR050772NIAMS NIH HHS R01 AR050772
6 · The paper itself

Abstract

T cell functional differentiation is mediated by lineage-specific transcription factors. T helper 17 (Th17) has been recently identified as a distinct Th lineage mediating tissue inflammation. Retinoic acid receptor-related orphan receptor gamma (ROR gamma) was shown to regulate Th17 differentiation; ROR gamma deficiency, however, did not completely abolish Th17 cytokine expression. Here, we report Th17 cells highly expressed another related nuclear receptor, ROR alpha, induced by transforming growth factor-beta and interleukin-6 (IL-6), which is dependent on signal transducer and activator of transcription 3. Overexpression of ROR alpha promoted Th17 differentiation, possibly through the conserved noncoding sequence 2 in Il17-Il17f locus. ROR alpha deficiency resulted in reduced IL-17 expression in vitro and in vivo. Furthermore, ROR alpha and ROR gamma coexpression synergistically led to greater Th17 differentiation. Double deficiencies in ROR alpha and ROR gamma globally impaired Th17 generation and completely protected mice against experimental autoimmune encephalomyelitis. Therefore, Th17 differentiation is directed by two lineage-specific nuclear receptors, ROR alpha and ROR gamma.

Indexed as

AnimalsCell DifferentiationCell LineageElectrophoretic Mobility Shift AssayEncephalomyelitis, Autoimmune, ExperimentalFemaleInterleukin-17MiceMice, Mutant StrainsNuclear Receptor Subfamily 1, Group F, Member 1Nuclear Receptor Subfamily 1, Group F, Member 3Receptors, Cytoplasmic and NuclearReceptors, Retinoic AcidReceptors, Thyroid HormoneReverse Transcriptase Polymerase Chain ReactionT-Lymphocytes, Helper-InducerInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 1Nuclear Receptor Subfamily 1, Group F, Member 3Receptors, Cytoplasmic and NuclearReceptors, Retinoic AcidReceptors, Thyroid HormoneRorc protein, mouseTrans-Activators

Identifiers

PMID18164222
PMCPMC2587175
OpenAlexW2091451666

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.