Evidence map›Paper›PMID 30084830›Full record

ArticleDiabetes2018

Type I and II Interferon Receptors Differentially Regulate Type 1 Diabetes Susceptibility in Male Versus Female NOD Mice.

Javier A Carrero, Nicholas D Benshoff, Kimberly Nalley, Emil R Unanue

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Diabetes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 38 citations in OpenAlex.

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  9. Immune Sexual Dimorphism: Connecting the Dots.Physiology (Bethesda, Md.) · 2022
    Review
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  11. 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

4 authors at 1 institution in 1 country.

Javier A CarreroDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO jacarrer@wustl.edu unanue@wustl.edu.ORCID 0000-0001-7712-6160
Nicholas D BenshoffDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO.
Kimberly NalleyDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO.
Emil R UnanueDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO jacarrer@wustl.edu unanue@wustl.edu.
Washington University in St. Louis · US

Funding

DIABETOGENIC MOLECULE I-AG7--CHEMISTRY AND BIOLOGYR01DK058177 · NIDDK · WASHINGTON UNIVERSITY · PI UNANUE, EMIL RAPHAEL · 2000 to 2020
$7.8M
INDUCTION OF UNRESPONSIVENESS TO ALLOGRAFTSR01AI014551 · NIAID · NEW ENGLAND DEACONESS HOSPITAL · PI MONACO, ANTHONY P · 1985 to 2004
$1.5M
Induction of tolerance to allograftsR56AI014551 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MONACO, ANTHONY P · 2005 to 2005
$383k
NIAID NIH HHS R01 AI014551NIAID NIH HHS R56 AI014551NIDDK NIH HHS R01 DK058177
6 · The paper itself

Abstract

The role of interferons, either pathogenic or protective, during autoimmune diabetes remains controversial. Herein, we examine the progression of diabetes in NOD mice lacking the type I (IFNAR) or type II (IFNGR) interferon receptor and, for the first time, in mice deficient in both receptors (double knockout [DKO]). All mice were bred, maintained, and monitored in a single specific pathogen-free facility with high female and low male diabetes incidence. Our expectation was that removal of interferon signaling would reduce autoimmune destruction. However, examination of diabetes incidence in the IFNAR- and IFNGR-deficient NOD mice showed a reduction in females and an increase in males. In DKO mice, diabetes occurred only in female mice, at decreased incidence and with delayed kinetics. These results show that interferons act as both positive and negative modulators of type 1 diabetes disease risk dependent on sex.

Indexed as

AgingAnimalsAutoimmune DiseasesDiabetes Mellitus, Type 1Disease-Free SurvivalDisease ProgressionFemaleIslets of LangerhansLeukocytesMaleMice, Inbred NODMice, KnockoutReceptor, Interferon alpha-betaSex CharacteristicsSpecific Pathogen-Free OrganismsIfnar1 protein, mouseIfnar2 protein, mouseReceptor, Interferon alpha-beta

Identifiers

PMID30084830
PMCPMC6110319
OpenAlexW2810005033

What OpenQuestion holds

Textmetadata
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.