Evidence map›Paper›PMID 39971758›Full record

ArticleScientific reports2025

Activated type 17 helper T cells affect tofacitinib treatment outcomes.

Yuki Ito, Daisuke Watanabe, Norihiro Okamoto, Haruka Miyazaki, Eri Tokunaga, Yuna Ku, Makoto Ooi, Namiko Hoshi, Michitaka Kohashi, Maki Kanzawa and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
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

11 authors.

Yuki ItoDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Daisuke WatanabeDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan. daisuke@med.kobe-u.ac.jp.
Norihiro OkamotoDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Haruka MiyazakiDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Eri TokunagaDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Yuna KuDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Makoto OoiDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Namiko HoshiDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.
Michitaka KohashiDepartment of Gastroenterology, Kakogawa Central City Hospital, Kakogawa, Hyogo, Japan.
Maki KanzawaDepartment of Diagnostic Pathology, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Yuzo KodamaDivision of Gastroenterology, Department of Internal Medicine, Kobe University Hospital, Kobe, Japan.

Funding

Grant-in-Aid for Early-Career Scientists 22K15966
6 · The paper itself

Abstract

The incidence of ulcerative colitis (UC) is on the rise also in Japan. Simultaneously, therapeutic options, including biologics and Janus kinase (JAK) inhibitors, have significantly expanded over the past decade. Although tofacitinib (TOF), one of JAK inhibitors, is a viable option for patients with moderate to severe UC, there is insufficient data to predict responsiveness of TOF treatment. The present study aimed to determine whether the infiltration of IL-17 A-positive mononuclear cells into the colonic mucosa can predict responsiveness to TOF treatment. Patients with UC who underwent TOF treatment were divided into responder and failure groups. Subsequently, we conducted a comparative analysis to identify differences in the infiltration of IL-17 A-positive cells into the colonic mucosa through immunohistochemical examination of colon biopsy samples. The proportion of IL-17 A positive mononuclear cells in colon biopsy samples was significantly higher in the failure group than among responders (38.2% vs. 21.2%). Consistent with this finding, our re-analysis of RNA sequence datasets available in the Gene Expression Omnibus (GEO) database suggested that TOF exerts a more pronounced influence on Th1 cells compared with IL-17-producing Th17 cells. In summary, an abundance of IL-17 A-positive mononuclear cells in the colonic mucosa has the potential to predict the responsiveness to TOF treatment.

Indexed as

Colitis, UlcerativePiperidinesPyrimidinesTh17 CellsAdultAgedColonFemaleHumansInterleukin-17Intestinal MucosaJanus Kinase InhibitorsMaleMiddle AgedProtein Kinase InhibitorsTreatment OutcomeIL17A protein, humanInterleukin-17Janus Kinase InhibitorsPiperidinesProtein Kinase InhibitorsPyrimidinestofacitinib

Identifiers

PMID39971758
PMCPMC11840122

What OpenQuestion holds

Textmetadata
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.