Evidence map›Paper›PMID 36508655›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

FXR mediates ILC-intrinsic responses to intestinal inflammation.

Ting Fu, Yuwenbin Li, Tae Gyu Oh, Fritz Cayabyab, Nanhai He, Qin Tang, Sally Coulter, Morgan Truitt, Paul Medina, Mingxiao He and 6 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 55 citations in OpenAlex.

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  9. Dysregulated immunometabolism in gut inflammation.Acta biochimica et biophysica Sinica · 2026
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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

16 authors at 2 institutions in 2 countries.

Ting FuGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Yuwenbin LiGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Tae Gyu OhGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-2756-3546
Fritz CayabyabGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Nanhai HeGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Qin TangGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Sally CoulterStorr Liver Centre, Westmead Institute for Medical Research and Sydney Medical School, University of Sydney, Westmead NSW 2145, Australia.
Morgan TruittGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Paul MedinaGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Mingxiao HeGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Ruth T YuGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-9527-9627
Annette AtkinsGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0003-3583-4091
Ye ZhengImmunobiology and Microbial Pathogenesis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.
Christopher LiddleStorr Liver Centre, Westmead Institute for Medical Research and Sydney Medical School, University of Sydney, Westmead NSW 2145, Australia.ORCID 0000-0003-3936-6790
Michael DownesGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-6351-9585
Ronald M EvansGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-9986-5965
Salk Institute for Biological Studies · USThe University of Sydney · AU

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Reuben Shaw · 1985 to 2026
$82.8M
Yeast Genetics and Stress Response Genes-BiomedicalP42ES010337 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TUKEY, ROBERT H · 2000 to 2022
$69.8M
Transcriptional GenomicsP01HL088093 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WITZTUM, JOSEPH L. · 2008 to 2018
$26.4M
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR37DK057978 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2000 to 2019
$16.0M
Hormonal Regulation of Mammalian Gene ExpressionR01DK057978 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2021 to 2024
$2.6M
Cancer Research UK SU2C-AACR-DT-20-16NCI NIH HHS P30 CA014195NHLBI NIH HHS P01 HL088093NIDDK NIH HHS R01 DK057978NIDDK NIH HHS R37 DK057978NIEHS NIH HHS P42 ES010337
6 · The paper itself

Abstract

The pleiotropic actions of the Farnesoid X Receptor (FXR) are required for gut health, and reciprocally, reduced intestinal FXR signaling is seen in inflammatory bowel diseases (IBDs). Here, we show that activation of FXR selectively in the intestine is protective in inflammation-driven models of IBD. Prophylactic activation of FXR restored homeostatic levels of pro-inflammatory cytokines, most notably IL17. Importantly, these changes were attributed to FXR regulation of innate lymphoid cells (ILCs), with both the inflammation-driven increases in ILCs, and ILC3s in particular, and the induction of

Indexed as

Immunity, InnateInflammatory Bowel DiseasesCytokinesHumansInflammationLymphocytesCytokinesbile acidsFXRIL17inflammatory bowel diseaseinnate lymphoid cells

Identifiers

PMID36508655
PMCPMC9907109
OpenAlexW4311663427

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.