Evidence map›Paper›PMID 27748438›Full record

ArticleScientific reports2016

Loss of interleukin 33 expression in colonic crypts - a potential marker for disease remission in ulcerative colitis.

Mona Dixon Gundersen, Rasmus Goll, Johanna Hol, Trine Olsen, Renathe Rismo, Sveinung W Sørbye, Olav Sundnes, Guttorm Haraldsen, Jon Florholmen

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  6. Intestinal Regulatory T Cells.Advances in experimental medicine and biology · 2021
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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

9 authors at 4 institutions in 1 country.

Mona Dixon GundersenResearch Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT The Arctic University of Norway, and the University Hospital of North Norway, Tromsø, Norway.
Rasmus GollResearch Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT The Arctic University of Norway, and the University Hospital of North Norway, Tromsø, Norway.
Johanna HolDept. of Pathology and Jebsen Inflammation Research Centre, University of Oslo and Oslo University Hospital Rikshospitalet, Oslo, Norway.
Trine OlsenResearch Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT The Arctic University of Norway, and the University Hospital of North Norway, Tromsø, Norway.
Renathe RismoResearch Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT The Arctic University of Norway, and the University Hospital of North Norway, Tromsø, Norway.
Sveinung W SørbyeResearch Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT The Arctic University of Norway, and the University Hospital of North Norway, Tromsø, Norway.
Olav SundnesDept. of Pathology and Jebsen Inflammation Research Centre, University of Oslo and Oslo University Hospital Rikshospitalet, Oslo, Norway.
Guttorm HaraldsenDept. of Pathology and Jebsen Inflammation Research Centre, University of Oslo and Oslo University Hospital Rikshospitalet, Oslo, Norway.
Jon FlorholmenResearch Group of Gastroenterology and Nutrition, Department of Clinical Medicine, UiT The Arctic University of Norway, and the University Hospital of North Norway, Tromsø, Norway.
University Hospital of North Norway · NOUiT The Arctic University of Norway · NOUniversity of Oslo · NOOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin 33 (IL-33) is a cytokine preferentially elevated in acute ulcerative colitis (UC), inferring a role in its pathogenesis. The role of IL-33 in intestinal inflammation is incompletely understood, with both pro-inflammatory and regulatory properties described. There are also conflicting reports on cellular sources and subcellular location of IL-33 in the colonic mucosa, justifying a closer look at IL-33 expression in well-defined clinical stages of UC. A total of 50 study participants (29 UC patients and 21 healthy controls) were included from a prospective cohort of inflammatory bowel disease patients treated to disease remission with infliximab, a tumour necrosis factor alpha (TNF) inhibitor. To our knowledge this is the first study examining mucosal IL-33 expression before and after anti-TNF therapy. In colonic mucosal biopsies we found a 3-fold increase in IL-33 gene expression comparing acute UC to healthy controls (p < 0.01). A significant reduction of IL33 between acute UC and disease remission was observed when TNF normalised in the mucosa (p = 0.02). Immunostaining revealed IL-33 in the nuclei of epithelial cells of scattered colonic crypts in acute disease, while at disease remission, IL-33 was undetectable, a novel finding suggesting that enterocyte-derived IL-33 is induced and maintained by inflammatory mediators.

Indexed as

Gene ExpressionAdultAgedBiomarkersCase-Control StudiesColitis, UlcerativeFemaleHumansImmunologic FactorsInterleukin-33Intestinal MucosaMaleMiddle AgedRNA, MessengerTumor Necrosis Factor-alphaBiomarkersImmunologic FactorsInterleukin-33RNA, MessengerTumor Necrosis Factor-alpha

Identifiers

PMID27748438
PMCPMC5066310
OpenAlexW2537329389

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Registered trials

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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.