Evidence map›Paper›PMID 30410494›Full record

ArticleFrontiers in immunology2018

Plasmacytoid Dendritic Cells Are Largely Dispensable for the Pathogenesis of Experimental Inflammatory Bowel Disease.

Catherine M Sawai, Lee Serpas, Antonio Galvao Neto, Geunhyo Jang, Ali Rashidfarrokhi, Roland Kolbeck, Miguel A Sanjuan, Boris Reizis, Vanja Sisirak

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
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  4. Pathophysiology of Inflammatory Bowel Disease: Innate Immune System.International journal of molecular sciences · 2023
    Review
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  6. Review
  7. Review
  8. 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

9 authors at 3 institutions in 2 countries.

Catherine M SawaiDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
Lee SerpasDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
Antonio Galvao NetoDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
Geunhyo JangDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
Ali RashidfarrokhiDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
Roland KolbeckDepartment of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, MD, United States.
Miguel A SanjuanDepartment of Respiratory, Inflammation and Autoimmunity, MedImmune LLC, Gaithersburg, MD, United States.
Boris ReizisDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
Vanja SisirakDepartment of Pathology, New York University School of Medicine, New York, NY, United States.
New York University · USCentre National de la Recherche Scientifique · FRUniversité de Bordeaux · FR

Funding

MEDICAL SCIENTIST TRAININGT32GM007308 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PHILIPS, MARK REID · 1985 to 2019
$23.2M
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
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR01AI072571 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2008 to 2017
$4.1M
NIAID NIH HHS R01 AI072571NIAID NIH HHS R37 AI072571NIAID NIH HHS T32 AI100853NIGMS NIH HHS T32 GM007308
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a chronic inflammatory condition caused by an aberrant immune response to microbial components of the gastrointestinal tract. Plasmacytoid dendritic cells (pDCs) are innate immune cells specialized in the production of type I interferons and were recently implicated in the pathogenesis of autoimmune disorders such as lupus and scleroderma. While pDCs were shown to infiltrate intestinal mucosa of IBD patients and proposed to participate in intestinal inflammation, their net contribution to the disease remains unclear. We addressed this question by targeting the pDC-specific transcription factor TCF4 (E2-2) in experimental IBD caused by deficiency of Wiskott-Aldrich syndrome protein (WASP) or of interleukin-10 (IL-10). Monoallelic

Indexed as

AnimalsColitisDendritic CellsHumansImmunity, InnateInflammatory Bowel DiseasesInterleukin-10Lupus NephritisMaleMiceMice, Inbred C57BLMice, KnockoutModels, AnimalTranscription Factor 4Wiskott-Aldrich Syndrome ProteinInterleukin-10Tcf4 protein, mouseTranscription Factor 4Wiskott-Aldrich Syndrome Proteinautoimmune diseasecolitisInflammatory bowel disease (IBD)Interferon Type IPlasmacytoid dendritic cell (PDC)

Identifiers

PMID30410494
PMCPMC6209677
OpenAlexW2896993572

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.