Evidence map›Paper›PMID 19538249›Full record

ReviewImmunology2009

The aryl hydrocarbon receptor: a perspective on potential roles in the immune system.

Emily A Stevens, Joshua D Mezrich, Christopher A Bradfield

Open access · greenAbstract readReview
In one paragraph

Review in Immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 215 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
215citing papers in PubMed, 1 pooled it
10.2field-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

215 citing papers in PubMed, 1 synthesis or guideline pooled it, 400 citations in OpenAlex.

  1. Pooled it
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  15. Pharmaceuticals (Basel, Switzerland) · 2024
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155 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Emily A StevensUniversity of Wisconsin School of Medicine and Public Health, Madison, WI 53706-1599, USA.
Joshua D Mezrich
Christopher A Bradfield
University of Wisconsin–Madison · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
INTEGRATED TRAINING FOR PHYSICIAN-SCIENTISTST32GM008692 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BURKARD, MARK E · 1998 to 2020
$10.3M
Characterization of the Ah Receptor Signaling PathwayR37ES005703 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI BRADFIELD, CHRISTOPHER A · 2002 to 2011
$4.1M
CHARACTERIZATION OF THE AH RECEPTOR SIGNALING PATHWAYR01ES005703 · NIEHS · UNIVERSITY OF WISCONSIN MADISON · PI BRADFIELD, CHRISTOPHER A · 1996 to 2001
$786k
Genetic and Genomic Analyses of Dioxin-induced Cleft PalateF30ES015416 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI STEVENS, EMILY A · 2006 to 2008
$94k
MOLECULAR CLONING OF AH-RECEPTOR POLYMORPHSR29ES005703 · NIEHS · NORTHWESTERN UNIVERSITY · PI BRADFIELD, CHRISTOPHER A · 1991 to 1995
–
MODULATION OF CHEMOKINE EXPRESSION BY OXIDATIVE STRESSF32ES005703 · NIEHS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHI, MICHAEL M · 1995 to 1995
–
NCI NIH HHS P30 CA014520NCI NIH HHS P30-CA014520NIEHS NIH HHS ES005703NIEHS NIH HHS F30 ES015416NIEHS NIH HHS F30-ES015416NIEHS NIH HHS F32 ES005703NIEHS NIH HHS R01 ES005703NIEHS NIH HHS R37 ES005703NIGMS NIH HHS T32 GM008692
6 · The paper itself

Abstract

The aryl hydrocarbon receptor (AHR) is a protein best known for its role in mediating toxicity. Over 30 years of research has uncovered additional roles for the AHR in xenobiotic metabolism and normal vascular development. Activation of the AHR has long been known to cause immunotoxicity, including thymic involution. Recent data suggesting a role for the AHR in regulatory T-cell (Treg) and T-helper 17 (Th17) cell development have only added to the excitement about this biology. In this review, we will attempt to illustrate what is currently known about AHR biology in the hope that data from fields as diverse as evolutionary biology and pharmacology will help elucidate the mechanism by which AHR modifies immune responses. We also will discuss the complexities of AHR pharmacology and genetics that may influence future studies of AHR in the immune system.

Indexed as

AnimalsEvolution, MolecularInflammationMiceMice, Mutant StrainsReceptors, Aryl HydrocarbonSignal TransductionT-Lymphocytes, RegulatoryReceptors, Aryl Hydrocarbon

Identifiers

PMID19538249
PMCPMC2712099
OpenAlexW2019103072

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.