Evidence map›Paper›PMID 30347820›Full record

ArticleInternational journal of molecular sciences2018

Type I Interferon Signaling Is Required for Dacryoadenitis in the Nonobese Diabetic Mouse Model of Sjögren Syndrome.

Yury Chaly, Jennifer Y Barr, David A Sullivan, Helen E Thomas, Thomas C Brodnicki, Scott M Lieberman

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Mechanisms of Disease in Sjögren Syndrome-New Developments and Directions.International journal of molecular sciences · 2020
    Article
  11. Article
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

6 authors at 3 institutions in 2 countries.

Yury ChalyStead Family Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA. yvchaly@gmail.com.
Jennifer Y BarrStead Family Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA. jennifer-barr@uiowa.edu.ORCID 0000-0002-1688-730X
David A SullivanDepartment of Ophthalmology, Schepens Eye Research Institute of Massachusetts Eye and Ear, Harvard Medical School, Boston, MA 02114, USA. david.sullivan@schepens.harvard.edu.ORCID 0000-0002-3424-3778
Helen E ThomasDepartment of Medicine, St. Vincent's Hospital, St. Vincent's Institute, The University of Melbourne, Fitzroy, Victoria 3065, Australia. hthomas@svi.edu.au.
Thomas C BrodnickiDepartment of Medicine, St. Vincent's Hospital, St. Vincent's Institute, The University of Melbourne, Fitzroy, Victoria 3065, Australia. tbrodnicki@svi.edu.au.ORCID 0000-0003-2294-315X
Scott M LiebermanStead Family Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA. scott-lieberman@uiowa.edu.ORCID 0000-0003-4082-7582
University of Iowa · USThe University of Melbourne · AUMassachusetts Eye and Ear Infirmary · US

Funding

Cytokines driving T cell dysregulation in lacrimal gland autoimmunityR01EY027731 · NEI · UNIVERSITY OF IOWA · PI LIEBERMAN, SCOTT MATTHEW · 2018 to 2022
$2.4M
National Health and Medical Research Council 1037321National Health and Medical Research Council 1042735NEI NIH HHS R01 EY027731NIH HHS EY027731NIH HHS EY05612
6 · The paper itself

Abstract

Nonobese diabetic (NOD) mice spontaneously develop lacrimal and salivary gland autoimmunity similar to human Sjögren syndrome. In both humans and NOD mice, the early immune response that drives T-cell infiltration into lacrimal and salivary glands is poorly understood. In NOD mice, lacrimal gland autoimmunity spontaneously occurs only in males with testosterone playing a role in promoting lacrimal gland inflammation, while female lacrimal glands are protected by regulatory T cells (Tregs). The mechanisms of this male-specific lacrimal gland autoimmunity are not known. Here, we studied the effects of Treg depletion in hormone-manipulated NOD mice and lacrimal gland gene expression to determine early signals required for lacrimal gland inflammation. While Treg-depletion was not sufficient to drive dacryoadenitis in castrated male NOD mice, chemokines (

Indexed as

AnimalsCells, CulturedChemokine CCL19Chemokine CXCL9DacryocystitisFemaleInterferon Type ILacrimal ApparatusMaleMiceMice, Inbred NODMice, SCIDSignal TransductionSjogren's SyndromeT-Lymphocytes, RegulatoryChemokine CCL19Chemokine CXCL9Interferon Type Ichemokineslacrimal glandsnonobese diabetic miceregulatory T cellsSjögren syndrometype I interferon

Identifiers

PMID30347820
PMCPMC6214106
OpenAlexW2895970986

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.