Evidence map›Paper›PMID 26213712›Full record

ArticleCellular and molecular gastroenterology and hepatology2015

Dysregulated intrahepatic CD4

Sara Omenetti, Marco Brogi, Wendy A Goodman, Colleen M Croniger, Saada Eid, Alex Y Huang, Giacomo Laffi, Tania Roskams, Fabio Cominelli, Massimo Pinzani and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Endoplasmic Reticulum Stress Regulates Hepatic Bile Acid Metabolism in Mice.Cellular and molecular gastroenterology and hepatology · 2017
    Article
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 at 5 institutions in 4 countries.

Sara OmenettiDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; "DENOThe" Center, University of Florence, Florence, Italy.
Marco BrogiDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; "DENOThe" Center, University of Florence, Florence, Italy.
Wendy A GoodmanDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Colleen M CronigerDepartment of Nutrition, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Saada EidDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Alex Y HuangDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Giacomo Laffi"DENOThe" Center, University of Florence, Florence, Italy.
Tania RoskamsDepartment of Morphology and Molecular Pathology, University of Leuven, Leuven, Belgium.
Fabio CominelliDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; "DENOThe" Center, University of Florence, Florence, Italy.
Massimo PinzaniDepartment of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; "DENOThe" Center, University of Florence, Florence, Italy ; UCL Institute for Liver and Digestive Health, Royal Free Hospital, London, UK.
Theresa T PizarroDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, USA ; "DENOThe" Center, University of Florence, Florence, Italy.
Case Western Reserve University · USUniversity of Florence · ITUniversity School · USKU Leuven · BEThe Royal Free Hospital · GB

Funding

Ubiquitination Pathways Mediating Chronic Intestinal InflammationP01DK091222 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI COMINELLI, FABIO · 2011 to 2020
$16.5M
The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI Theresa Torres Pizarro · 2015 to 2026
$15.6M
MECHANISMS OF EXPERIMENTAL CROHNS DISEASER01DK055812 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI COMINELLI, FABIO · 1999 to 2019
$4.9M
CYTOKINES AND INFLAMMATORY BOWEL DISEASER01DK042191 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI COMINELLI, FABIO, PIZARRO, THERESA TORRES · 1995 to 2022
$4.7M
CYTOKINES AND INFLAMMATORY BOWEL DISEASER37DK042191 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI COMINELLI, FABIO · 1999 to 2009
$3.8M
Role of IL-18 in Crohn's Disease (CD)R01DK056762 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI PIZARRO, THERESA TORRES · 2000 to 2009
$2.3M
Cytokines and Inflammatory Bowel DiseaseR56DK042191 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI COMINELLI, FABIO · 2010 to 2010
$504k
Mechanisms underlying sex differences in the pathogenesis of IBDR21AI102269 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI PIZARRO, THERESA TORRES · 2012 to 2013
$420k
NIAID NIH HHS R21 AI102269NIDDK NIH HHS P01 DK091222NIDDK NIH HHS P30 DK097948NIDDK NIH HHS R01 DK042191NIDDK NIH HHS R01 DK055812NIDDK NIH HHS R01 DK056762NIDDK NIH HHS R37 DK042191NIDDK NIH HHS R56 DK042191
6 · The paper itself

Abstract

BACKGROUND AND

aimsLiver inflammation is a common extraintestinal manifestation of inflammatory bowel disease (IBD); however, whether liver involvement is a consequence of a primary intestinal defect or results from alternative pathogenic processes remains unclear. Therefore, we sought to determine the potential pathogenic mechanism(s) of concomitant liver inflammation in an established murine model of IBD.

methodsLiver inflammation and immune cell subsets were characterized in ileitis-prone SAMP1/YitFc (SAMP) and AKR/J (AKR) control mice, lymphocyte-depleted SAMP (SAMPx

resultsSurprisingly, prominent inflammation was detected in 4-wk-old SAMP livers, prior to histologic evidence of ileitis, while both disease phenotypes were absent in age-matched AKRs. SAMP liver disease was characterized by abundant infiltration of lymphocytes, required for hepatic inflammation to occur, a Th1-skewed environment, and phenotypically-activated CD4

conclusionsActivated intrahepatic CD4

Indexed as

hepatic CD4+ T-cellsIBD-associated liver inflammationliver sinusoidal endothelial cellsregulatory T-cellsSAMP1/YitFc mice

Identifiers

PMID26213712
PMCPMC4511857
OpenAlexW1530421426

What OpenQuestion holds

Textmetadata
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.