Evidence map›Paper›PMID 30692988›Full record

ArticleFrontiers in immunology2018

Maturing Human CD127+ CCR7+ PDL1+ Dendritic Cells Express AIRE in the Absence of Tissue Restricted Antigens.

Joannah R Fergusson, Michael D Morgan, Melanie Bruchard, Leonie Huitema, Balthasar A Heesters, Vincent van Unen, Jan Piet van Hamburg, Nicole N van der Wel, Daisy Picavet, Frits Koning and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  20. Review
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

15 authors at 7 institutions in 3 countries.

Joannah R FergussonDepartment of Experimental Immunology, Academic Medical Center, Amsterdam, Netherlands.
Michael D MorganWellcome Sanger Institute, Hinxton, United Kingdom.
Melanie BruchardDepartment of Experimental Immunology, Academic Medical Center, Amsterdam, Netherlands.
Leonie HuitemaDepartment of Rheumatology & Clinical Immunology and Department of Experimental Immunology, Amsterdam Infection & Immunity Institute, University of Amsterdam, Amsterdam, Netherlands.
Balthasar A HeestersDepartment of Experimental Immunology, Academic Medical Center, Amsterdam, Netherlands.
Vincent van UnenLeiden University Medical Center, Leiden, Netherlands.
Jan Piet van HamburgDepartment of Rheumatology & Clinical Immunology and Department of Experimental Immunology, Amsterdam Infection & Immunity Institute, University of Amsterdam, Amsterdam, Netherlands.
Nicole N van der WelEMCA, Medical Biology, Academic Medical Center, Amsterdam, Netherlands.
Daisy PicavetEMCA, Medical Biology, Academic Medical Center, Amsterdam, Netherlands.
Frits KoningLeiden University Medical Center, Leiden, Netherlands.
Sander W TasDepartment of Rheumatology & Clinical Immunology and Department of Experimental Immunology, Amsterdam Infection & Immunity Institute, University of Amsterdam, Amsterdam, Netherlands.
Mark S AndersonUCSF Diabetes Center, University of California, San Francisco, San Francisco, CA, United States.
John C MarioniWellcome Sanger Institute, Hinxton, United Kingdom.
Georg A HolländerLaboratory of Developmental Immunology, Weatherall Institute of Molecular Medicine and Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Hergen SpitsDepartment of Experimental Immunology, Academic Medical Center, Amsterdam, Netherlands.
Academic Medical Center · NLLeiden University Medical Center · NLCancer Research UK Cambridge Center · GBMRC Weatherall Institute of Molecular Medicine · GBUniversity of Amsterdam · NLUniversity of California, San Francisco · USWellcome Sanger Institute · GB

Funding

Developing eTACs as a Novel Method of Tolerance in Type 1 DiabetesR01DK101622 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S · 2014 to 2018
$1.7M
Cancer Research UK 17197Cancer Research UK 22231NIDDK NIH HHS R01 DK101622Wellcome TrustWellcome Trust 105045/Z/14/Z
6 · The paper itself

Abstract

Expression of the Autoimmune regulator (AIRE) outside of the thymus has long been suggested in both humans and mice, but the cellular source in humans has remained undefined. Here we identify AIRE expression in human tonsils and extensively analyzed these "extra-thymic AIRE expressing cells" (eTACs) using combinations of flow cytometry, CyTOF and single cell RNA-sequencing. We identified AIRE+ cells as dendritic cells (DCs) with a mature and migratory phenotype including high levels of antigen presenting molecules and costimulatory molecules, and specific expression of CD127, CCR7, and PDL1. These cells also possessed the ability to stimulate and re-stimulate T cells and displayed reduced responses to toll-like receptor (TLR) agonists compared to conventional DCs. While expression of

Indexed as

AIRE ProteinB7-H1 AntigenCell CommunicationCells, CulturedChild, PreschoolDendritic CellsHumansInfantInfant, NewbornInterleukin-7 Receptor alpha SubunitLymphocyte ActivationPalatine TonsilPrimary Cell CultureReceptors, CCR7T-LymphocytesTranscription FactorsAIRE ProteinB7-H1 AntigenCCR7 protein, humanCD274 protein, humanInterleukin-7 Receptor alpha SubunitReceptors, CCR7Transcription FactorsAIREdendritic cellsmaturationPDL1tissue restricted antigen

Identifiers

PMID30692988
PMCPMC6340304
OpenAlexW2910614064

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.