Evidence map›Paper›PMID 32194571›Full record

ArticleFrontiers in immunology2020

Phosphatase PTPN22 Regulates Dendritic Cell Homeostasis and cDC2 Dependent T Cell Responses.

Harriet A Purvis, Fiona Clarke, Anna B Montgomery, Chloe Colas, Jack A Bibby, Georgina H Cornish, Xuezhi Dai, Diana Dudziak, David J Rawlings, Rose Zamoyska and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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 5 institutions in 4 countries.

Harriet A PurvisFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Fiona ClarkeFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Anna B MontgomeryFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Chloe ColasFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Jack A BibbyFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Georgina H CornishFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Xuezhi DaiSeattle Children's Research Institute, Seattle, WA, United States.
Diana DudziakLaboratory of Dendritic Cell Biology, Department of Dermatology, Friedrich-Alexander University of Erlangen, Erlangen, Germany.
David J RawlingsSeattle Children's Research Institute, Seattle, WA, United States.
Rose ZamoyskaCentre for Immunity, Infection and Evolution, Institute of Immunology and Infection Research, University of Edinburgh, Edinburgh, United Kingdom.
Pierre GuermonprezFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
Andrew P CopeFaculty of Life Sciences and Medicine, Centre for Inflammation Biology and Cancer Immunology, King's College London, London, United Kingdom.
King's College London · GBUniversity of Washington · USCentre for Immunity, Infection and Evolution · GBFriedrich-Alexander-Universität Erlangen-Nürnberg · DEInserm · FR

Funding

An integrated strategy to define the functional and synergistic impact of T1D causal variantsDP3DK111802 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI RAWLINGS, DAVID J · 2016 to 2016
$4.4M
Defining the functional impact of T1D genes in mouse and man: a unified strategyDP3DK097672 · NIDDK · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI BUCKNER, JANE HOYT · 2012 to 2013
$4.4M
Biotechnology and Biological Sciences Research Council BB/M029735/1Cancer Research UK C57672/A22369Department of HealthNIDDK NIH HHS DP3 DK097672NIDDK NIH HHS DP3 DK111802Versus Arthritis 20218Versus Arthritis 20525Wellcome Trust 096669AIAWellcome Trust 205014/Z/16/Z
6 · The paper itself

Abstract

Dendritic cells (DCs) are specialized antigen presenting cells that instruct T cell responses through sensing environmental and inflammatory danger signals. Maintaining the homeostasis of the multiple functionally distinct conventional dendritic cells (cDC) subsets that exist

Indexed as

AnimalsAutoimmunityDendritic CellsHomeostasisImmune ToleranceLymphocyte ActivationMiceMice, TransgenicPolymorphism, Single NucleotideProtein Tyrosine Phosphatase, Non-Receptor Type 22T-Lymphocytes, Helper-InducerProtein Tyrosine Phosphatase, Non-Receptor Type 22Ptpn22 protein, mouseautoimmunitycDC2dendritic cellhomeostasispolymorphismproliferationPTPN22T follicular helper cell

Identifiers

PMID32194571
PMCPMC7065600
OpenAlexW3009308211

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.