Evidence map›Paper›PMID 28593185›Full record

ArticleCellular and molecular gastroenterology and hepatology2017

Induction of Colonic Regulatory T Cells by Mesalamine by Activating the Aryl Hydrocarbon Receptor.

Kyoko Oh-Oka, Yuko Kojima, Koichiro Uchida, Kimiko Yoda, Kayoko Ishimaru, Shotaro Nakajima, Jun Hemmi, Hiroshi Kano, Yoshiaki Fujii-Kuriyama, Ryohei Katoh and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

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  17. In silico analysis of3 Biotech · 2022
    Article
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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

12 authors at 3 institutions in 1 country.

Kyoko Oh-OkaDepartment of Immunology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Yuko KojimaThe Laboratory of Morphology and Image Analysis, Research Support Center, Juntendo University School of Medicine, Tokyo, Japan.
Koichiro UchidaAtopy Research Center, Juntendo University School of Medicine, Tokyo, Japan.
Kimiko YodaDepartment of Pathology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Kayoko IshimaruDepartment of Immunology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Shotaro NakajimaDepartment of Immunology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Jun HemmiFood Science Research Laboratories, Division of Research and Development, Meiji Co, Ltd, Kanagawa, Japan.
Hiroshi KanoFood Science Research Laboratories, Division of Research and Development, Meiji Co, Ltd, Kanagawa, Japan.
Yoshiaki Fujii-KuriyamaMedical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Ryohei KatohDepartment of Pathology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Hiroyuki ItoFood Science Research Laboratories, Division of Research and Development, Meiji Co, Ltd, Kanagawa, Japan.
Atsuhito NakaoDepartment of Immunology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
University of Yamanashi · JPJuntendo University · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsMesalamine is a first-line drug for treatment of inflammatory bowel diseases (IBD). However, its mechanisms are not fully understood. CD4

methodsWe examined the frequencies of Tregs in the colons of wild-type mice, mice deficient for aryl hydrocarbon receptor (

resultsTreatment of wild-type mice with mesalamine increased the accumulation of Tregs in the colon and up-regulated the AhR target gene

conclusionsWe propose a novel anti-inflammatory mechanism of mesalamine for colitis: induction of Tregs in the colon via the AhR pathway, followed by TGF-β activation.

Indexed as

AhR, aryl hydrocarbon receptorAryl Hydrocarbon ReceptorBM, bone marrowDSS, dextran sodium sulfateELISA, enzyme-linked immunosorbent assayFBS, fetal bovine serumFITC, fluorescein isothiocyanateIBD, inflammatory bowel diseaseIFN, interferonIL, interleukinLPL, lamina propria lymphocytesmAb, monoclonal antibodyMesalamineMLN, mesenteric lymph nodesPBS, phosphate-buffered salineQ-PCR, quantitative polymerase chain reactionRegulatory T CellsRPMI, Roswell Park Memorial InstituteTCDD, 2,3,7,8-tetrachlorodibenzo-p-dioxinTGF, transforming growth factorTGF-βTNF, tumor necrosis factorTregs, regulatory T cellsWT, wild-typeXRE, xenobiotic responsive element

Identifiers

PMID28593185
PMCPMC5453907
OpenAlexW2605857994

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.