Evidence map›Paper›PMID 25160819›Full record

ArticleMucosal immunology2015

IL-23 activates innate lymphoid cells to promote neonatal intestinal pathology.

Lili Chen, Zhengxiang He, Erik Slinger, Gerold Bongers, Taciana L S Lapenda, Michelle E Pacer, Jingjing Jiao, Monique F Beltrao, Alan J Soto, Noam Harpaz and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

41 citing papers in PubMed, 59 citations in OpenAlex.

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  14. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
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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

18 authors at 4 institutions in 1 country.

Lili Chen *Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Zhengxiang He *Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Erik SlingerImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Gerold BongersImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Taciana L S LapendaImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Michelle E PacerImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Jingjing JiaoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Monique F BeltraoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Alan J SotoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Noam HarpazDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Ronald E GordonDepartment of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Jordi C OchandoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mohamed OukkaDepartment of Pediatrics, University of Washington, Seattle, WA 98101, USA.
Alina Cornelia IugaDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Stephen W ChensueDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48105, USA.
Julie Magarian BlanderImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Glaucia C FurtadoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sergio A LiraImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Icahn School of Medicine at Mount Sinai · USColumbia University Irving Medical Center · USUniversity of Washington · USVA Ann Arbor Healthcare System · US

Funding

THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSEP01DK072201 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HARPAZ, NOAM · 2006 to 2015
$14.6M
Molecular pathogenesis of intestinal serrated polypsR01CA161373 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2011 to 2020
$3.7M
Role of apoptosis in the intestinal epithelium during homeostasis and diseaseR01DK111862 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLANDER, JULIE MAGARIAN · 2017 to 2020
$1.5M
NCI NIH HHS R01 CA161373NIDDK NIH HHS P01 DK072201NIDDK NIH HHS R01 DK111862
6 · The paper itself

Abstract

Interleukin-23 (IL-23) responsive group 3 innate lymphoid cells (ILC3s) have been implicated in immune homeostasis and pathogenesis in the adult, but little is known about their roles in the newborn. Here we show that IL-23 promotes conversion of embryonic intestinal Lin(-)IL-23R(+)Thy1(+) cells into IL-22-producing Thy1(+)Sca-1(hi) ILC3s in vitro. Gut-specific expression of IL-23 also activated and expanded Thy1(+)Sca-1(hi) ILC3s, which produced IL-22, IL-17, interferon gamma (IFN-γ), and granulocyte-macrophage colony-stimulating factor (GM-CSF) and were distinct from canonical CD4(+) lymphoid tissue inducer (LTi) cells. These ILC3s accumulated under the epithelium in intercellular adhesion molecule (ICAM)-1-positive cell aggregates together with neutrophils that disrupted the epithelium, leading to the formation of discrete intestinal erosions, bleeding, and neonatal death. Genetic and antibody depletion of ILC3s rescued the mice from neonatal death. Antibiotic treatment of pregnant mothers and offspring prolonged survival of IL-23 transgenic mice, suggesting a role for the commensal flora on ILC3-induced pathogenesis. Our results reveal a novel role for the IL-23-ILC3s axis in the pathogenesis of neonatal intestinal inflammation.

Indexed as

Immunity, InnateAnimalsAntigens, SurfaceCytokinesGene ExpressionHumansImmunophenotypingInterleukin-23Intestinal MucosaIntestinesLymphocytesMiceMice, TransgenicNeutrophil InfiltrationNeutrophilsPermeabilityAntigens, SurfaceCytokinesInterleukin-23

Identifiers

PMID25160819
PMCPMC4326561
OpenAlexW1967840465

What OpenQuestion holds

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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.