Evidence map›Paper›PMID 31873294›Full record

ArticleNature immunology2020

The neuropeptide VIP confers anticipatory mucosal immunity by regulating ILC3 activity.

Cyril Seillet, Kylie Luong, Julie Tellier, Nicolas Jacquelot, Rui Dong Shen, Peter Hickey, Verena C Wimmer, Lachlan Whitehead, Kelly Rogers, Gordon K Smyth and 3 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

125 citing papers in PubMed, 221 citations in OpenAlex.

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  15. Neuroimmune Circuits in Allergic Diseases.Annual review of immunology · 2025
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65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Cyril SeilletWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia. seillet@wehi.edu.au.ORCID http://orcid.org/0000-0002-0941-8679
Kylie LuongWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-1459-2604
Julie TellierWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Nicolas JacquelotWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Rui Dong ShenWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Peter HickeyWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-8153-6258
Verena C WimmerWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Lachlan WhiteheadWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Kelly RogersWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Gordon K SmythWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-9221-2892
Alexandra L GarnhamWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Matthew E RitchieWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-7383-0609
Gabrielle T BelzWalter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia. belz@wehi.edu.au.ORCID http://orcid.org/0000-0002-9660-9587
The University of Melbourne · AUThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group 3 innate lymphoid cell (ILC3)-mediated production of the cytokine interleukin-22 (IL-22) is critical for the maintenance of immune homeostasis in the gastrointestinal tract. Here, we find that the function of ILC3s is not constant across the day, but instead oscillates between active phases and resting phases. Coordinate responsiveness of ILC3s in the intestine depended on the food-induced expression of the neuropeptide vasoactive intestinal peptide (VIP). Intestinal ILC3s had high expression of the G protein-coupled receptor vasoactive intestinal peptide receptor 2 (VIPR2), and activation by VIP markedly enhanced the production of IL-22 and the barrier function of the epithelium. Conversely, deficiency in signaling through VIPR2 led to impaired production of IL-22 by ILC3s and increased susceptibility to inflammation-induced gut injury. Thus, intrinsic cellular rhythms acted in synergy with the cyclic patterns of food intake to drive the production of IL-22 and synchronize protection of the intestinal epithelium through a VIP-VIPR2 pathway in ILC3s.

Indexed as

PeriodicityAnimalsEatingImmunity, InnateImmunity, MucosalLymphocytesLymphocyte SubsetsMiceMice, Inbred C57BLVasoactive Intestinal PeptideVasoactive Intestinal Peptide

Identifiers

PMID31873294
OpenAlexW2995023574

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.