Evidence map›Paper›PMID 25706098›Full record

ReviewAnnual review of immunology2015

Interleukin-22: immunobiology and pathology.

Jarrod A Dudakov, Alan M Hanash, Marcel R M van den Brink

Open access · bronzeAbstract readReview
In one paragraph

Review in Annual review of immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 528 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
528citing papers in PubMed, 1 pooled it
29.3field-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

528 citing papers in PubMed, 1 synthesis or guideline pooled it, 874 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  12. IL-22 synergizes with IL-17 to promote mucosal inflammation and bone loss.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
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468 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

3 authors at 2 institutions in 3 countries.

Jarrod A DudakovImmunology Program and.
Alan M Hanash
Marcel R M van den Brink
Memorial Sloan Kettering Cancer Center · USMonash University · AU

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI PAMER, ERIC G. · 1985 to 2023
$59.0M
Strategies to enhance immune reconstitution after bone marrow transplantR01HL069929 · NHLBI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI VAN DEN BRINK, MARCEL R M · 2002 to 2015
$7.0M
Strategies to Enhance Lymphoid Recovery After Radiation-Induced InjuryR01AI080455 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI VAN DEN BRINK, MARCEL R M · 2008 to 2012
$2.6M
IL-22 in Thymic RegenerationR01AI101406 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI VAN DEN BRINK, MARCEL R M · 2012 to 2016
$2.5M
Mucosal Immunity and Microbiota in Intestinal Graft-versus-Host DiseaseR01AI100288 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI VAN DEN BRINK, MARCEL R M · 2012 to 2016
$2.2M
IL-22 in epithelial regeneration after allogeneic transplantK08HL115355 · NHLBI · SLOAN-KETTERING INST CAN RESEARCH · PI HANASH, ALAN M · 2012 to 2016
$719k
Investigating the role of interleukin-22 in thymus functionK99CA176376 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI DUDAKOV, JARROD · 2013 to 2013
$179k
NCI NIH HHS K99 CA176376NCI NIH HHS K99-CA176376NCI NIH HHS P01 CA023766NCI NIH HHS P01-CA023766NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA072720NHLBI NIH HHS K08 HL115355NHLBI NIH HHS K08-HL115355NHLBI NIH HHS R01 HL069929NHLBI NIH HHS R01-HL069929NIAID NIH HHS HHSN272200900059CNIAID NIH HHS R01 AI080455NIAID NIH HHS R01-AI080455NIAID NIH HHS R01 AI100288NIAID NIH HHS R01-AI100288NIAID NIH HHS R01 AI101406NIAID NIH HHS R01-AI101406
6 · The paper itself

Abstract

Interleukin-22 (IL-22) is a recently described IL-10 family cytokine that is produced by T helper (Th) 17 cells, γδ T cells, NKT cells, and newly described innate lymphoid cells (ILCs). Knowledge of IL-22 biology has evolved rapidly since its discovery in 2000, and a role for IL-22 has been identified in numerous tissues, including the intestines, lung, liver, kidney, thymus, pancreas, and skin. IL-22 primarily targets nonhematopoietic epithelial and stromal cells, where it can promote proliferation and play a role in tissue regeneration. In addition, IL-22 regulates host defense at barrier surfaces. However, IL-22 has also been linked to several conditions involving inflammatory tissue pathology. In this review, we assess the current understanding of this cytokine, including its physiologic and pathologic effects on epithelial cell function.

Indexed as

AnimalsDisease SusceptibilityGene Expression RegulationHumansInterleukin-22InterleukinsLymphocytesOrgan SpecificitySignal TransductionInterleukin-22Interleukinsepithelial cellsinterleukin-22tissue regeneration

Identifiers

PMID25706098
PMCPMC4407497
OpenAlexW2169378111

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.