Evidence map›Paper›PMID 33355506›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2021

Tofacitinib inhibits inflammatory cytokines from ulcerative colitis and healthy mucosal explants and is associated with pSTAT1/3 reduction in T-cells.

Rhonda M Brand, Beverley A Moore, Ashley Zyhowski, Aaron Siegel, Shikhar Uttam, E Jeffrey Metter, Jarret Engstrom, Randall E Brand, Nabanita Biswas, David C Whitcomb and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

13 authors at 4 institutions in 1 country.

Rhonda M BrandUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Beverley A MooreUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Ashley ZyhowskiMagee-Womens Research Institute and Foundation, Pittsburgh, Pennsylvania.
Aaron SiegelMagee-Womens Research Institute and Foundation, Pittsburgh, Pennsylvania.
Shikhar UttamUniversity of Tennessee Health Science Center, Memphis, Tennessee.
E Jeffrey MetterUniversity of Tennessee Health Science Center, Memphis, Tennessee.
Jarret EngstromMagee-Womens Research Institute and Foundation, Pittsburgh, Pennsylvania.
Randall E BrandUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Nabanita BiswasUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
David C WhitcombUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID https://orcid.org/0000-0002-4462-1410
David G BinionUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Marc SchwartzUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Ian McGowanUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
University of Pittsburgh · USMagee-Womens Research Institute · USUniversity of Tennessee Health Science Center · USMoore College of Art and Design · US

Funding

Project 3: PREVENT: A first-in-human clinical trial of Griffithsin, an HIV entryU19AI113182 · NIAID · UNIVERSITY OF LOUISVILLE · PI BRAND, RHONDA METTER · 2014 to 2018
$14.8M
HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) U19AI113182NIAID NIH HHS U19 AI113182
6 · The paper itself

Abstract

Poor translatability of animal disease models has hampered the development of new inflammatory bowel disorder (IBD) therapeutics. We describe a preclinical, ex vivo system using freshly obtained and well-characterized human colorectal tissue from patients with ulcerative colitis (UC) and healthy control (HC) participants to test potential therapeutics for efficacy and target engagement, using the JAK/STAT inhibitor tofacitinib (TOFA) as a model therapeutic. Colorectal biopsies from HC participants and patients with UC were cultured and stimulated with multiple mitogens ± TOFA. Soluble biomarkers were detected using a 29-analyte multiplex ELISA. Target engagement in CD3

Indexed as

Bayes TheoremBiomarkersColitis, UlcerativeCytokinesGene Expression RegulationHumansIntestinal MucosaJanus KinasesPiperidinesProtein Kinase InhibitorsPyrimidinesSTAT1 Transcription FactorSTAT3 Transcription FactorT-LymphocytesBiomarkersCytokinesJanus KinasesPiperidinesProtein Kinase InhibitorsPyrimidinesSTAT1 protein, humanSTAT1 Transcription FactorSTAT3 protein, humanSTAT3 Transcription FactortofacitinibbiomarkerbiopsyIBDJAK/STATphenotypepSTATulcerative colitisUMAP

Identifiers

PMID33355506
PMCPMC8202239
OpenAlexW3115992670

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.