Evidence map›Paper›PMID 28412753›Full record

ArticleOncotarget2017

Vitamin D increases programmed death receptor-1 expression in Crohn's disease.

Mia Bendix, Stinne Greisen, Anders Dige, Christian L Hvas, Nina Bak, Søren P Jørgensen, Jens F Dahlerup, Bent Deleuran, Jørgen Agnholt

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Vitamin D for the treatment of inflammatory bowel disease.The Cochrane database of systematic reviews · 2023
    Pooled it
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  8. 1α,25(OH)Journal for immunotherapy of cancer · 2022
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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 1 institution in 1 country.

Mia BendixDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Stinne GreisenDepartment of Immunology, Institute of Biomedicine, Aarhus University, Aarhus, Denmark.
Anders DigeDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Christian L HvasDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Nina BakDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Søren P JørgensenDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Jens F DahlerupDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Bent DeleuranDepartment of Immunology, Institute of Biomedicine, Aarhus University, Aarhus, Denmark.
Jørgen AgnholtDepartment of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
Aarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVitamin D modulates inflammation in Crohn's disease (CD). Programmed death (PD)-1 receptor contributes to the maintenance of immune tolerance. Vitamin D might modulate PD-1 signalling in CD.

aimTo investigate PD-1 expression on T cell subsets in CD patients treated with vitamin D or placebo.

methodsWe included 40 CD patients who received 1200 IU vitamin D3 for 26 weeks or placebo and eight healthy controls. Peripheral blood mononuclear cells (PBMCs) and plasma were isolated at baseline and week 26. The expressions of PD-1, PD-L1, and surface activation markers were analysed by flow cytometry. Soluble PD-1 plasma levels were measured by ELISA.

resultsPD-1 expression upon T cell stimulation was increased in CD4+CD25+int T cells in vitamin D treated CD patients from 19% (range 10 - 39%) to 29% (11 - 79%)(p = 0.03) compared with placebo-treated patients. Vitamin D treatment, but not placebo, decreased the expression of the T cell activation marker CD69 from 42% (31 - 62%) to 33% (19 - 54%)(p = 0.01). Soluble PD-1 levels were not influenced by vitamin D treatment.

conclusionsVitamin D treatment increases CD4+CD25+int T cells ability to up-regulate PD-1 in response to activation and reduces the CD69 expression in CD patients.

Indexed as

Gene Expression RegulationAdultAgedCells, CulturedCrohn DiseaseFemaleHumansLeukocytes, MononuclearLymphocyte ActivationMaleMiddle AgedProgrammed Cell Death 1 ReceptorT-Lymphocyte SubsetsVitamin DYoung AdultProgrammed Cell Death 1 ReceptorVitamin DCrohn’s diseaseImmune responseImmunityImmunology and Microbiology SectionPD-1T cellsvitamin D

Identifiers

PMID28412753
PMCPMC5421837
OpenAlexW2590425834

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.