Evidence map›Paper›PMID 28125663›Full record

ArticlePloS one2017

IL-22R Ligands IL-20, IL-22, and IL-24 Promote Wound Healing in Diabetic db/db Mice.

Ganesh Kolumam, Xiumin Wu, Wyne P Lee, Jason A Hackney, Jose Zavala-Solorio, Vineela Gandham, Dimitry M Danilenko, Puneet Arora, Xiaoting Wang, Wenjun Ouyang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
5.1field-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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

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  11. Inflammation, diabetic foot and related treatments.Frontiers in endocrinology · 2025
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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

10 authors.

Ganesh KolumamDepartment of Biomedical Imaging, Genentech, South San Francisco, California, United States of America.
Xiumin WuDepartment of Immunology, Genentech, South San Francisco, California, United States of America.
Wyne P LeeDepartment of Immunology, Genentech, South San Francisco, California, United States of America.
Jason A HackneyDepartment of Bioinformatics and Computational Biology, Genentech, South San Francisco, California, United States of America.
Jose Zavala-SolorioDepartment of Molecular Biology, Genentech, South San Francisco, California, United States of America.
Vineela GandhamDepartment of Biomedical Imaging, Genentech, South San Francisco, California, United States of America.
Dimitry M DanilenkoDepartment of Safety Assessment Pathology, Genentech, South San Francisco, California, United States of America.
Puneet AroraDepartment of Early Clinical Development, Genentech, South San Francisco, California, United States of America.
Xiaoting WangDepartment of Immunology, Genentech, South San Francisco, California, United States of America.
Wenjun OuyangDepartment of Immunology, Genentech, South San Francisco, California, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic foot ulcers (DFU) are one of the major complications in type II diabetes patients and can result in amputation and morbidity. Although multiple approaches are used clinically to help wound closure, many patients still lack adequate treatment. Here we show that IL-20 subfamily cytokines are upregulated during normal wound healing. While there is a redundant role for each individual cytokine in this subfamily in wound healing, mice deficient in IL-22R, the common receptor chain for IL-20, IL-22, and IL-24, display a significant delay in wound healing. Furthermore, IL-20, IL-22 and IL-24 are all able to promote wound healing in type II diabetic db/db mice. Mechanistically, when compared to other growth factors such as VEGF and PDGF that accelerate wound healing in this model, IL-22 uniquely induced genes involved in reepithelialization, tissue remodeling and innate host defense mechanisms from wounded skin. Interestingly, IL-22 treatment showed superior efficacy compared to PDGF or VEGF in an infectious diabetic wound model. Taken together, our data suggest that IL-20 subfamily cytokines, particularly IL-20, IL-22, and IL-24, might provide therapeutic benefit for patients with DFU.

Indexed as

AnimalsDiabetes Mellitus, Type 2Diabetic FootGene Expression RegulationHumansImmunoglobulin Fc FragmentsInterleukin-22Interleukin-24InterleukinsLigandsMiceMice, Inbred NODReceptors, InterleukinWound HealingWound InfectionImmunoglobulin Fc Fragmentsinterleukin 20Interleukin-22interleukin-22 receptorInterleukin-24InterleukinsLigandsReceptors, Interleukin

Identifiers

PMID28125663
PMCPMC5268431
OpenAlexW2582813880

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.