Evidence map›Paper›PMID 28573508›Full record

ArticleDigestive diseases and sciences2017

Crossover Subsets of CD4

Ji Li, Aito Ueno, Marietta Iacucci, Miriam Fort Gasia, Humberto B Jijon, Remo Panaccione, Gilaad G Kaplan, Paul L Beck, Joanne Luider, Herman W Barkema and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Digestive diseases and sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  14. Article
  15. Intestinal Regulatory T Cells.Advances in experimental medicine and biology · 2021
    Article
  16. Review
  17. Role of PD-L1 in Gut Mucosa Tolerance and Chronic Inflammation.International journal of molecular sciences · 2020
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 3 countries.

Ji LiGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Aito UenoGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada. aueno@ucalgary.ca.ORCID 0000-0002-9967-7200
Marietta IacucciGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Miriam Fort GasiaGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Humberto B JijonGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Remo PanaccioneGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Gilaad G KaplanGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Paul L BeckGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Joanne LuiderCalgary Laboratory Services, Calgary, AB, Canada.
Herman W BarkemaGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
Jiaming QianDepartment of Gastroenterology, Peking Union Medical College Hospital, Beijing, China.
Xianyong GuiCalgary Laboratory Services, Calgary, AB, Canada.
Subrata GhoshGastrointestinal Research Group/Department of Medicine, HSC1838, University of Calgary, 2500 University Dr. NW, Calgary, AB, Canada.
University of Calgary · CACalgary Laboratory Services · CAChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHovhannisyan et al. first showed evidence of plasticity between Treg and Th17 in the inflamed intestine of Crohn's disease (CD) patients. Our previous report suggests that the inflammatory cytokine milieu generates IL-17

aimThe aim of this study was to characterize a variety of helper T cell crossover population, not limited to IL-17

methodsFresh colonoscopic biopsies were obtained from patients with CD (n = 50) and ulcerative colitis (UC, n = 32) and from healthy controls (HC, n = 25). LP mononuclear cells were assessed for intracellular cytokines and transcription factors such as IFNγ, IL-13, IL-17, IL-22, T-bet, Gata-3, RORγt, and Foxp3 using multicolor flow cytometry to detect subsets of LP CD4

resultsPatients with IBD demonstrated increased crossover populations in IL-17

conclusionIBD patients exhibit the increased crossover populations in LP Treg cells toward Th2 and Th17 compared to HC. The prevalence of Treg/Th2 crossover populations is associated with clinical disease score of IBD.

Indexed as

AdultCD4-Positive T-LymphocytesCohort StudiesColitis, UlcerativeCrohn DiseaseCross-Sectional StudiesFemaleHumansIntestinal MucosaMaleMiddle AgedMucous MembraneT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsCrohn’s diseaseRegulatory T cellsT cell crossover populationTh17Th22Ulcerative colitis

Identifiers

PMID28573508
OpenAlexW2620766890

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.