Evidence map›Paper›PMID 26883847›Full record

ArticleScientific reports2016

Hyporesponsiveness to the anti-inflammatory action of interleukin-10 in type 2 diabetes.

Julianne C Barry, Soroush Shakibakho, Cody Durrer, Svetlana Simtchouk, Kamaldeep K Jawanda, Sylvia T Cheung, Alice L Mui, Jonathan P Little

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 3 pooled it
5.3field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 3 syntheses or guidelines pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Review
  7. Insulin Resistance and Inflammation.International journal of molecular sciences · 2026
    Review
  8. Observational
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Lower Serum IL-10 Linked to Oral Manifestations in Diabetes Patients.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

4 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 1 institution in 1 country.

Julianne C BarrySchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, BC, Canada.
Soroush ShakibakhoDepartment of Surgery, University of British Columbia, Vancouver, BC, Canada.
Cody DurrerSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, BC, Canada.
Svetlana SimtchoukSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, BC, Canada.
Kamaldeep K JawandaDepartment of Surgery, University of British Columbia, Vancouver, BC, Canada.
Sylvia T CheungDepartment of Surgery, University of British Columbia, Vancouver, BC, Canada.
Alice L MuiDepartment of Surgery, University of British Columbia, Vancouver, BC, Canada.
Jonathan P LittleSchool of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, BC, Canada.
University of British Columbia · CA

Funding

Canadian Institutes of Health Research (201412MSH-340087-205631Canadian Institutes of Health Research MOP-133415
6 · The paper itself

Abstract

Chronic low-grade inflammation contributes to the pathology and complications of type 2 diabetes (T2D). Interleukin-10 (IL10), an anti-inflammatory cytokine, is suggested to play a protective role in T2D. However, the impact of T2D on IL10 function has not been previously assessed. We examined the ability of IL10 to inhibit inflammation in human T2D immune cells and explored underlying mechanisms using macrophage models. IL10 was less effective at inhibiting tumour necrosis factor (TNF)-α secretion in T2D whole blood cultures, which was not explained by altered IL10 receptor surface expression. These findings were observed in macrophages exposed to high glucose, which demonstrated similar IL10 resistance or hyporesponsiveness. These findings were also not explained by changes in IL10 receptor protein or other downstream signaling proteins. High glucose was also shown to impair the ability of IL10 to activate STAT3, a downstream signaling protein of IL10. Treatment with the SHIP1 agonist, AQX-MN100, reversed IL10 hyporesponsiveness in macrophages cultured in high glucose and showed equal effectiveness at different glucose conditions. This data supports the idea that IL10 hyporesponsiveness may contribute to chronic inflammation in T2D. These novel findings suggest that strategies aimed to overcome IL10 hyporesponsiveness may hold therapeutic potential for reducing inflammation in T2D.

Indexed as

AdultAgedAnimalsAnti-Inflammatory AgentsBlood GlucoseCell LineCytokinesDiabetes Mellitus, Type 2FemaleGene ExpressionHumansInflammationInflammation MediatorsInterleukin-10Interleukin-10 Receptor alpha SubunitMacrophagesAnti-Inflammatory AgentsAQX MN100Blood GlucoseCytokinesInflammation MediatorsINPP5D protein, humanInterleukin-10Interleukin-10 Receptor alpha SubunitPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPolycyclic CompoundsSTAT3 Transcription Factor

Identifiers

PMID26883847
PMCPMC4756700
OpenAlexW2409158180

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.