Evidence map›Paper›PMID 23791644›Full record

ArticleImmunity2013

Global chromatin state analysis reveals lineage-specific enhancers during the initiation of human T helper 1 and T helper 2 cell polarization.

R David Hawkins, Antti Larjo, Subhash K Tripathi, Ulrich Wagner, Ying Luu, Tapio Lönnberg, Sunil K Raghav, Leonard K Lee, Riikka Lund, Bing Ren and 2 more

Abstract read
In one paragraph

Article in Immunity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 94 citations in OpenAlex.

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  18. TNature reviews. Immunology · 2018
    Review
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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

12 authors at 3 institutions in 2 countries.

R David HawkinsDivision of Medical Genetics and Department of Genome Sciences, Department of Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA. rdhawk@uw.edu
Antti Larjo
Subhash K Tripathi
Ulrich Wagner
Ying Luu
Tapio Lönnberg
Sunil K Raghav
Leonard K Lee
Riikka Lund
Bing Ren
Harri Lähdesmäki
Riitta Lahesmaa
Åbo Akademi University · FIUniversity of California San Diego · USTampere University · FI

Funding

The San Diego Epigenome CenterU01ES017166 · NIEHS · LUDWIG INSTITUTE FOR CANCER RES LTD · PI REN, BING · 2008 to 2013
$16.3M
NIEHS NIH HHS U01 ES017166
6 · The paper itself

Abstract

Naive CD4⁺ T cells can differentiate into specific helper and regulatory T cell lineages in order to combat infection and disease. The correct response to cytokines and a controlled balance of these populations is critical for the immune system and the avoidance of autoimmune disorders. To investigate how early cell-fate commitment is regulated, we generated the first human genome-wide maps of histone modifications that reveal enhancer elements after 72 hr of in vitro polarization toward T helper 1 (Th1) and T helper 2 (Th2) cell lineages. Our analysis indicated that even at this very early time point, cell-specific gene regulation and enhancers were at work directing lineage commitment. Further examination of lineage-specific enhancers identified transcription factors (TFs) with known and unknown T cell roles as putative drivers of lineage-specific gene expression. Lastly, an integrative analysis of immunopathogenic-associated SNPs suggests a role for distal regulatory elements in disease etiology.

Indexed as

Cell DifferentiationCell LineageChromatinGenetic Predisposition to DiseaseGenome-Wide Association StudyHistonesHumansImmune System DiseasesPolymorphism, Single NucleotidePromoter Regions, GeneticTh1 CellsTh1-Th2 BalanceTh2 CellsChromatinHistones

Identifiers

PMID23791644
PMCPMC4607036
OpenAlexW1964267076

What OpenQuestion holds

Textmetadata
LicenceTDM
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.