Evidence map›Paper›PMID 32454024›Full record

ArticleImmunity2020

Plasmacytoid Dendritic Cells and Type I Interferon Promote Extrafollicular B Cell Responses to Extracellular Self-DNA.

Chetna Soni, Oriana A Perez, William N Voss, Joseph N Pucella, Lee Serpas, Justin Mehl, Krystal L Ching, Jule Goike, George Georgiou, Gregory C Ippolito and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

129 citing papers in PubMed, 179 citations in OpenAlex.

  1. Trial
  2. Trial
  3. InterferonFrontiers in immunology · 2020
    Trial
  4. Review
  5. The SLC15A4-TASL complex is essential for lupus development in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
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  16. Article
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69 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

12 authors at 3 institutions in 2 countries.

Chetna SoniDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Oriana A PerezDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
William N VossDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712, USA.
Joseph N PucellaDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Lee SerpasDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Justin MehlDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Krystal L ChingDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Jule GoikeDepartment of Chemical Engineering, University of Texas at Austin, Austin, TX 78712, USA.
George GeorgiouDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712, USA; Department of Chemical Engineering, University of Texas at Austin, Austin, TX 78712, USA.
Gregory C IppolitoDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX 78712, USA; Department of Oncology, Dell Medical School, University of Texas at Austin, Austin, TX 78712, USA.
Vanja SisirakCNRS-UMR 5164, ImmunoConcEpt, Université de Bordeaux, 33076 Bordeaux, France. Electronic address: vsisirak@immuconcept.org.
Boris ReizisDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA; Department of Medicine, New York University Grossman School of Medicine, New York, NY 10016, USA. Electronic address: boris.reizis@nyulangone.org.
New York University · USThe University of Texas at Austin · USCentre National de la Recherche Scientifique · FR

Funding

TRAINING PROGRAM IN MOLECULAR ONCOLOGY &IMMUNOLOGYT32CA009161 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CARROLL, WILLIAM L., LEVY, DAVID E · 1985 to 2020
$13.3M
Translational Center of Molecular Profiling in Preclinical and Established Lupus (COMPEL)P50AR070591 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P · 2017 to 2021
$6.7M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR37AI072571 · NIAID · UNIVERSITY OF CHICAGO · PI Boris Reizis · 2018 to 2026
$5.3M
Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
Mechanisms of DNA-Specific Autoimmunity in Systemic Lupus ErythematosusR01AR071703 · NIAMS · UNIVERSITY OF CHICAGO · PI Jill P Buyon, GEORGE Georgiou GEORGIOU · 2018 to 2026
$4.4M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR01AI072571 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2008 to 2017
$4.1M
Translational Basic and Clinical Research Training in RheumatologyT32AR069515 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jill P Buyon, Jose U. Scher · 2017 to 2026
$2.9M
Kinetic Characterization of Hematopoietic Stem Cell Differentiation During Homeostasis And Pathological ConditionsF32HL145997 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PUCELLA, JOSEPH NICHOLAS · 2019 to 2021
$176k
BCL11A in normal B-cell biology and malignancyF32CA110624 · NCI · UNIVERSITY OF TEXAS AUSTIN · PI IPPOLITO, GREGORY C · 2005 to 2007
$156k
Dynamic Spatiotemporal Analysis of Immune Cells in the Tumor MicroenvironmentF32CA232666 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PEREZ, ORIANA · 2018 to 2020
$150k
NCI NIH HHS F32 CA110624NCI NIH HHS F32 CA232666NCI NIH HHS T32 CA009161NHLBI NIH HHS F32 HL145997NIAID NIH HHS R01 AI072571NIAID NIH HHS R37 AI072571NIAID NIH HHS T32 AI100853NIAMS NIH HHS P50 AR070591NIAMS NIH HHS R01 AR071703NIAMS NIH HHS T32 AR069515
6 · The paper itself

Abstract

Class-switched antibodies to double-stranded DNA (dsDNA) are prevalent and pathogenic in systemic lupus erythematosus (SLE), yet mechanisms of their development remain poorly understood. Humans and mice lacking secreted DNase DNASE1L3 develop rapid anti-dsDNA antibody responses and SLE-like disease. We report that anti-DNA responses in Dnase1l3

Indexed as

Cell CommunicationAnimalsAntibodies, AntinuclearAutoantigensAutoimmunityBiomarkersB-LymphocytesCD40 LigandDendritic CellsDisease Models, AnimalDisease SusceptibilityDNAEndodeoxyribonucleasesFluorescent Antibody TechniqueGerminal CenterInterferon Type IAntibodies, AntinuclearAutoantigensBiomarkersCD40 LigandDNADnase1l3 protein, mouseEndodeoxyribonucleasesInterferon Type IToll-Like Receptor 7Toll-Like Receptor 9anti-DNA antibodiesDNASE1L3extrafollicular B cell responseplasmacytoid dendritic cellssystemic lupus erythematosusTLR7TLR9type I interferon

Identifiers

PMID32454024
PMCPMC7306002
OpenAlexW3026999446

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.