Evidence map›Paper›PMID 32294406›Full record

ArticleImmunity2020

Insulin-Like Growth Factors Are Key Regulators of T Helper 17 Regulatory T Cell Balance in Autoimmunity.

Daniel DiToro, Stacey N Harbour, Jennifer K Bando, Gloria Benavides, Steven Witte, Vincent A Laufer, Carson Moseley, Jeffery R Singer, Blake Frey, Henrietta Turner and 8 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 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
8.3field-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

108 citing papers in PubMed, 1 synthesis or guideline pooled it, 185 citations in OpenAlex.

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48 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

18 authors at 5 institutions in 2 countries.

Daniel DiToroDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Stacey N HarbourDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Jennifer K BandoDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Gloria BenavidesMitochondrial Medicine Laboratory, Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Steven WitteDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Vincent A LauferDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Carson MoseleyDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Jeffery R SingerDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Blake FreyDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Henrietta TurnerDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Jens BruningMax Plank Institute for Metabolism Research, Department of Neuronal Control of Metabolism, Cologne, Germany; Center for Endocrinology, Diabetes, and Preventive Medicine (CEDP), University Hospital Cologne, Cologne, Germany; Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD) and Center of Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Victor Darley-UsmarMitochondrial Medicine Laboratory, Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Min GaoInformatics Institute and Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Cheryl ConoverDivision of Endocrinology, Mayo Clinic, Rochester, MN 55905, USA.
Robin D HattonDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Stuart FrankDepartment of Medicine, Division of Endocrinology, Diabetes, and Metabolism, University of Alabama at Birmingham, Birmingham, AL 35203, USA; Department of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35203, USA.
Marco ColonnaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Casey T WeaverDepartments of Pathology, University of Alabama at Birmingham, Birmingham, AL 35203, USA; Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, University of Alabama at Birmingham, Birmingham, AL 35203, USA; Department of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35203, USA. Electronic address: cweaver@uabc.edu.
University of Alabama at Birmingham · USMitochondria Research and Medicine Society · USWashington University in St. Louis · USCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEWinnMed · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
Training Program in Rheumatic and Musculoskeletal Diseases ResearchT32AR069516 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI John D Mountz · 2016 to 2026
$2.6M
Specialization of Innate and Adaptive Immune Cells in Intestinal Barrier FunctionR01DK113789 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WEAVER, CASEY T · 2017 to 2021
$2.3M
Mechanisms Controlling Regulatory T cell Effector Function in IBDR01DK115172 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HATTON, ROBIN D, WEAVER, CASEY T · 2017 to 2020
$2.1M
A Novel Role for IGF-1 Receptor in Growth Hormone ActionR01DK107441 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FRANK, STUART J · 2016 to 2019
$1.3M
Th17 Pathway Plasticity in the Pathogenesis of Inflammatory Bowel DiseaseR01DK103744 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WEAVER, CASEY T · 2015 to 2018
$1.3M
Immune Checkpoints for Intestinal Innate Lymphoid CellsK99DK118110 · NIDDK · WASHINGTON UNIVERSITY · PI BANDO, JENNIFER KAORU · 2019 to 2020
$182k
NIAID NIH HHS T32 AI007051NIAMS NIH HHS T32 AR069516NIDDK NIH HHS K99 DK118110NIDDK NIH HHS P30 DK056341NIDDK NIH HHS P30 DK079626NIDDK NIH HHS R01 DK103744NIDDK NIH HHS R01 DK107441NIDDK NIH HHS R01 DK113789NIDDK NIH HHS R01 DK115172
6 · The paper itself

Abstract

Appropriate balance of T helper 17 (Th17) and regulatory T (Treg) cells maintains immune tolerance and host defense. Disruption of Th17-Treg cell balance is implicated in a number of immune-mediated diseases, many of which display dysregulation of the insulin-like growth factor (IGF) system. Here, we show that, among effector T cell subsets, Th17 and Treg cells selectively expressed multiple components of the IGF system. Signaling through IGF receptor (IGF1R) activated the protein kinase B-mammalian target of rapamycin (AKT-mTOR) pathway, increased aerobic glycolysis, favored Th17 cell differentiation over that of Treg cells, and promoted a heightened pro-inflammatory gene expression signature. Group 3 innate lymphoid cells (ILC3s), but not ILC1s or ILC2s, were similarly responsive to IGF signaling. Mice with deficiency of IGF1R targeted to T cells failed to fully develop disease in the experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis. Thus, the IGF system represents a previously unappreciated pathway by which type 3 immunity is modulated and immune-mediated pathogenesis controlled.

Indexed as

AutoimmunityAnimalsCell CommunicationCell DifferentiationCell LineageEncephalomyelitis, Autoimmune, ExperimentalFemaleGene Expression RegulationImmune ToleranceImmunity, InnateLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, TransgenicMyelin-Oligodendrocyte GlycoproteinIgf1r protein, mousemTOR protein, mouseMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsProto-Oncogene Proteins c-aktReceptor, IGF Type 1TOR Serine-Threonine KinasesCD4 T cellEAEIGF1Rinsulin-like growth factormultiple sclerosisTh17Treg

Identifiers

PMID32294406
PMCPMC8078727
OpenAlexW3015407511

What OpenQuestion holds

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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.