Evidence map›Paper›PMID 26802241›Full record

ArticleThe Journal of investigative dermatology2016

IL-33-Dependent Group 2 Innate Lymphoid Cells Promote Cutaneous Wound Healing.

Gregory D Rak, Lisa C Osborne, Mark C Siracusa, Brian S Kim, Kelvin Wang, Ardeshir Bayat, David Artis, Susan W Volk

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
9.3field-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

139 citing papers in PubMed, 216 citations in OpenAlex.

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  18. Cellular and molecular mechanisms of skin wound healing.Nature reviews. Molecular cell biology · 2024
    Review
  19. Article
  20. Interleukin-2-induced skin inflammation.European journal of immunology · 2024
    Article

79 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

8 authors at 3 institutions in 2 countries.

Gregory D RakPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Lisa C OsborneJill Roberts Institute for Research in IBD, Weill Cornell Medical College, Cornell University New York, New York, USA.
Mark C SiracusaPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Brian S KimPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Kelvin WangPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Ardeshir BayatPlastic & Reconstructive Surgery Research, Manchester Institute of Biotechnology, University of Manchester, Manchester, UK; Center for Dermatology, Institute of Inflammation and Repair, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
David ArtisJill Roberts Institute for Research in IBD, Weill Cornell Medical College, Cornell University New York, New York, USA. Electronic address: dartis@med.cornell.edu.
Susan W VolkDepartment of Clinical Studies-Philadelphia, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA. Electronic address: swvolk@vet.upenn.edu.
University of Pennsylvania · USCornell University · USUniversity of Manchester · GB

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
Transcriptomics and Repertoire ProfilingP01AI106697 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Scott Dexter Boyd · 2013 to 2026
$31.3M
Regulation of protective immunity following enteric viral infectionU01AI095608 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ARTIS, DAVID, SONNENBERG, GREGORY F · 2011 to 2025
$11.0M
Penn Dermatology Research Training ProgramT32AR007465 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice, David Joel Margolis · 1986 to 2026
$9.0M
Institutional Clinical and Translational Science AwardKL2RR024132 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$5.1M
Innate immunity and inflammation following helminth infectionR01AI074878 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ARTIS, DAVID · 2008 to 2019
$4.2M
Immuno-regulation of GI nematode infectionR01AI061570 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ARTIS, DAVID · 2004 to 2013
$4.1M
Regulation and function of innate lymphoid cells in the gutR01AI095466 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ARTIS, DAVID · 2011 to 2022
$3.7M
Regulation and function of innate lymphoid cells during influenza virus infectionR01AI102942 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ARTIS, DAVID · 2013 to 2017
$2.1M
Cytokine regulation of anti-helminth immunityR01AI097333 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI ARTIS, DAVID · 2012 to 2016
$2.0M
Innate Immune Regulation of Skin InflammationK08AR065577 · NIAMS · WASHINGTON UNIVERSITY · PI KIM, BRIAN · 2014 to 2018
$711k
Mesenchymal Stem Cell Application for Ischemic wound HealingK08AR053945 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI VOLK, SUSAN W · 2007 to 2011
$638k
NCRR NIH HHS KL2 RR024132NCRR NIH HHS KL2-RR024132NIAID NIH HHS AI061570NIAID NIH HHS AI074878NIAID NIH HHS AI095466NIAID NIH HHS AI095608NIAID NIH HHS AI097333NIAID NIH HHS AI102942NIAID NIH HHS AI106697NIAID NIH HHS F32 AI085828NIAID NIH HHS F32-AI085828NIAID NIH HHS K22 AI110573NIAID NIH HHS P01 AI106697NIAID NIH HHS R01 AI061570NIAID NIH HHS R01 AI074878NIAID NIH HHS R01 AI095466NIAID NIH HHS R01 AI097333NIAID NIH HHS R01 AI102942NIAID NIH HHS R21 AI087990NIAID NIH HHS U01 AI095608NIAMS NIH HHS K08 AR053945NIAMS NIH HHS K08AR053945NIAMS NIH HHS K08 AR065577NIAMS NIH HHS T32 AR007465NIAMS NIH HHS T32-AR007465NIDDK NIH HHS P30 DK050306NIDDK NIH HHS P30-DK050306
6 · The paper itself

Abstract

Breaches in the skin barrier initiate an inflammatory immune response that is critical for successful wound healing. Innate lymphoid cells (ILCs) are a recently identified population of immune cells that reside at epithelial barrier surfaces such as the skin, lung, and gut, and promote proinflammatory or epithelial repair functions after exposure to allergens, pathogens, or chemical irritants. However, the potential role of ILCs in regulating cutaneous wound healing remains undefined. Here, we demonstrate that cutaneous injury promotes an IL-33-dependent group 2 ILC (ILC2) response and that abrogation of this response impairs re-epithelialization and efficient wound closure. In addition, we provide evidence suggesting that an analogous ILC2 response is operational in acute wounds of human skin. Together, these results indicate that IL-33-responsive ILC2s are an important link between the cutaneous epithelium and the immune system, acting to promote the restoration of skin integrity after injury.

Indexed as

AnimalsBiopsy, NeedleDisease Models, AnimalHumansImmunity, InnateImmunohistochemistryInterleukin-33LymphocytesMiceMice, Inbred C57BLSkinWound HealingWounds and InjuriesInterleukin-33

Identifiers

PMID26802241
PMCPMC4731037
OpenAlexW1795019646

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.