Evidence map›Paper›PMID 33936048›Full record

ArticleFrontiers in immunology2021

Identification of a Sensitive Human Immunological Target of Aryl Hydrocarbon Receptor Activation: CD5

Lance K Blevins, Jiajun Zhou, Robert B Crawford, Norbert E Kaminski

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 35% 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, 10 citations in OpenAlex.

  1. 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

4 authors at 1 institution in 1 country.

Lance K BlevinsInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, United States.
Jiajun ZhouDepartment of Microbiology & Molecular Genetics, Michigan State University, East Lansing, MI, United States.
Robert B CrawfordDepartment of Toxicology & Pharmacology, Michigan State University, East Lansing, MI, United States.
Norbert E KaminskiInstitute for Integrative Toxicology, Michigan State University, East Lansing, MI, United States.
Michigan State University · US

Funding

VOLATILE ORGANIC CONTAMINANTS--QUANTIFYING THEIR MOVEMENT IN THE UNSATURATED ZONEP42ES004911 · NIEHS · MICHIGAN STATE UNIVERSITY · PI Brian P. Johnson · 1989 to 2026
$64.9M
NIEHS NIH HHS P42 ES004911
6 · The paper itself

Abstract

Xenobiotic-mediated activation of the aryl hydrocarbon receptor (AHR) is immunotoxic in a number of immune cell types, with the B cell being a well-established sensitive target. Recent advances have provided evidence that the B cell repertoire is a heterogeneous population, with subpopulations exhibiting vastly different cellular and functional phenotypes. Recent work from our laboratory identified the T cell specific kinase lck as being differentially regulated by

Indexed as

B7-H1 AntigenBasic Helix-Loop-Helix ProteinsB-Lymphocyte SubsetsCD5 AntigensCells, CulturedCytochrome P-450 CYP1A1HumansImmunity, InnateImmunoglobulin MLymphocyte Specific Protein Tyrosine Kinase p56(lck)PhenotypePolychlorinated DibenzodioxinsProgrammed Cell Death 1 Ligand 2 ProteinProgrammed Cell Death 1 ReceptorReceptors, Aryl HydrocarbonRepressor ProteinsAHR protein, humanAHRR protein, humanB7-H1 AntigenBasic Helix-Loop-Helix ProteinsCD274 protein, humanCD5 AntigensCYP1A1 protein, humanCytochrome P-450 CYP1A1Immunoglobulin MLCK protein, humanLymphocyte Specific Protein Tyrosine Kinase p56(lck)PDCD1LG2 protein, humanPDCD1 protein, humanPolychlorinated DibenzodioxinsProgrammed Cell Death 1 Ligand 2 ProteinProgrammed Cell Death 1 ReceptorReceptors, Aryl HydrocarbonRepressor ProteinsAHRhumanimmune suppressioninnate-like B cellsPD-1

Identifiers

PMID33936048
PMCPMC8082145
OpenAlexW3152560415

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.