Evidence map›Paper›PMID 25378593›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Cutting edge: Genetic variation in TLR1 is associated with Pam3CSK4-induced effector T cell resistance to regulatory T cell suppression.

Carmen Mikacenic, Anya Schneider, Frank Radella, Jane H Buckner, Mark M Wurfel

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  5. 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

5 authors at 1 institution in 1 country.

Carmen MikacenicDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington, Seattle, WA 98104; and cmikacen@uw.edu.ORCID http://orcid.org/0000-0001-8966-5161
Anya SchneiderTranslational Research Program, Benaroya Research Institute, Seattle, WA 98101.
Frank RadellaDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington, Seattle, WA 98104; and.
Jane H BucknerTranslational Research Program, Benaroya Research Institute, Seattle, WA 98101.
Mark M WurfelDivision of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington, Seattle, WA 98104; and.
University of Washington · US

Funding

Variation in Human Innate ImmunityU54AI057141 · NIAID · UNIVERSITY OF WASHINGTON · PI MANOIL, COLIN · 2003 to 2013
$102.3M
Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Tomas Vaisar · 1986 to 2026
$41.4M
Defining the role of altered cytokine signaling pathways on autoimmunityU01AI101990 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI BUCKNER, JANE HOYT · 2012 to 2016
$12.1M
Genetic control of gene expression during innate immune activationR01HL089807 · NHLBI · UNIVERSITY OF WASHINGTON · PI WURFEL, MARK M · 2007 to 2011
$2.6M
Influence of TLR1 Polymorphisms on T-Regulatory Cells in ARDSK23HL120896 · NHLBI · UNIVERSITY OF WASHINGTON · PI MIKACENIC, CARMEN R · 2014 to 2018
$881k
NHLBI NIH HHS K23 HL120896NHLBI NIH HHS K23 HL120896-01NHLBI NIH HHS R01 HL089807NHLBI NIH HHS R01 HL089807-01NIAID NIH HHS U01 AI101990NIAID NIH HHS U01 AI101990-01NIAID NIH HHS U54 AI057141NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

TLR play essential roles in the initiation and modulation of immune responses. TLR1/TLR2 heterodimers recognize triacylated bacterial lipopeptides, including the synthetic TLR1/2 lipopeptide Pam3CSK4. Genetic variation in TLR1 is associated with outcomes in diseases in which regulatory T cells (Treg) play a role, including asthma and allergy. To determine whether genetic polymorphisms in TLR1 are associated with alterations in Treg suppression of effector T cells (Teff), we performed in vitro suppression assays in healthy individuals with various haplotypes in TLR1. We show that functional genetic polymorphisms in TLR1 modify surface expression of TLR1 on T lymphocytes and confer enhanced Teff resistance to Treg suppression in the presence of Pam3CSK4. These effects are mediated, in part, by IL-6 and inhibited by blocking IL-6 signaling through STAT3. These findings suggest that TLR1 polymorphisms could influence immune-related disease through Teff resistance to Treg suppression.

Indexed as

Genetic VariationAllelesCell MembraneHaplotypesHumansImmunomodulationInterleukin-6LipopeptidesPolymorphism, Single NucleotideSTAT3 Transcription FactorT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsToll-Like Receptor 1Interleukin-6LipopeptidesPam(3)CSK(4) peptideSTAT3 Transcription FactorToll-Like Receptor 1

Identifiers

PMID25378593
PMCPMC4258445
OpenAlexW1841796142

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.