Evidence map›Paper›PMID 25183367›Full record

ArticleMucosal immunology2015

Lymphotoxin beta receptor signaling limits mucosal damage through driving IL-23 production by epithelial cells.

E Macho-Fernandez, E P Koroleva, C M Spencer, M Tighe, E Torrado, A M Cooper, Y-X Fu, A V Tumanov

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 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.8field-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

45 citing papers in PubMed, 76 citations in OpenAlex.

  1. Oral delivery of recombinantDrug delivery · 2026
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  13. IL-12 and IL-23 pathway inhibition in inflammatory bowel disease.Nature reviews. Gastroenterology & hepatology · 2023
    Review
  14. Article
  15. The star target in SLE: IL-17.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  16. Interference with LTβR signaling by tick saliva facilitates transmission of Lyme disease spirochetes.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. 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

8 authors at 2 institutions in 1 country.

E Macho-FernandezTrudeau Institute, Saranac Lake, New York, USA.
E P KorolevaTrudeau Institute, Saranac Lake, New York, USA.
C M SpencerTrudeau Institute, Saranac Lake, New York, USA.
M TigheTrudeau Institute, Saranac Lake, New York, USA.
E TorradoTrudeau Institute, Saranac Lake, New York, USA.
A M CooperTrudeau Institute, Saranac Lake, New York, USA.
Y-X FuDepartment of Pathology, The University of Chicago, Chicago, Illinois, USA.
A V TumanovTrudeau Institute, Saranac Lake, New York, USA.
Trudeau Institute · USUniversity of Chicago · US

Funding

Research Training in Immunology and Infectious DiseasesT32AI049823 · NIAID · TRUDEAU INSTITUTE, INC. · PI COOPER, ANDREA M · 2001 to 2015
$2.1M
TNF family members for lymph angiogenesis and lymph node hypertrophyR01CA141975 · NCI · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2010 to 2014
$1.6M
NCI NIH HHS CA141975NCI NIH HHS R01 CA141975NIAID NIH HHS T32 AI049823
6 · The paper itself

Abstract

The immune mechanisms regulating epithelial cell repair after injury remain poorly defined. We demonstrate here that lymphotoxin beta receptor (LTβR) signaling in intestinal epithelial cells promotes self-repair after mucosal damage. Using a conditional gene-targeted approach, we demonstrate that LTβR signaling in intestinal epithelial cells is essential for epithelial interleukin-23 (IL-23) production and protection against epithelial injury. We further show that epithelial-derived IL-23 promotes mucosal wound healing by inducing the IL-22-mediated proliferation and survival of epithelial cells and mucus production. Additionally, we identified CD4(-)CCR6(+)T-bet(-) RAR-related orphan receptor gamma t (RORγt)(+) lymphoid tissue inducer cells as the main producers of protective IL-22 after epithelial damage. Thus, our results reveal a novel role for LTβR signaling in epithelial cells in the regulation of intestinal epithelial cell homeostasis to limit mucosal damage.

Indexed as

Signal TransductionAnimalsColitisDisease Models, AnimalEpithelial CellsGene ExpressionHomeostasisInterleukin-22Interleukin-23InterleukinsIntestinal MucosaLymphotoxin beta ReceptorMiceMice, KnockoutT-Lymphocyte SubsetsWound HealingInterleukin-22Interleukin-23InterleukinsLymphotoxin beta Receptor

Identifiers

PMID25183367
PMCPMC4364000
OpenAlexW1972674066

What OpenQuestion holds

Textmetadata
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.