Evidence map›Paper›PMID 29889233›Full record

ArticleInflammatory bowel diseases2018

Implementation of Mass Cytometry as a Tool for Mechanism of Action Studies in Inflammatory Bowel Disease.

Christopher J Tyler, Tamara Pérez-Jeldres, Erik Ehinger, Brian Capaldo, Thangaraj Karuppuchamy, Joshua D Boyer, Derek Patel, Parambir Dulai, Brigid S Boland, Joanne Lannigan and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Inflammatory bowel diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Best Practices for Preparing a Single Cell Suspension from Solid Tissues for Flow Cytometry.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2019
    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

15 authors at 4 institutions in 2 countries.

Christopher J TylerInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Tamara Pérez-JeldresInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Erik EhingerFlow Cytometry Core Facility, La Jolla Institute of Allergy and Immunology, La Jolla, California.
Brian CapaldoFlow Cytometry Core Facility, University of Virginia, Charlottesville, Virginia.
Thangaraj KaruppuchamyInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Joshua D BoyerInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Derek PatelVA San Diego Healthcare System, San Diego, California.
Parambir DulaiInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Brigid S BolandInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Joanne LanniganFlow Cytometry Core Facility, University of Virginia, Charlottesville, Virginia.
Lars EckmannInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Peter B ErnstDivision of Comparative Pathology, Department of Pathology, University of California San Diego, La Jolla, California.
William J SandbornVA San Diego Healthcare System, San Diego, California.
Samuel B HoInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
Jesús Rivera-NievesInflammatory Bowel Disease Center, Division of Gastroenterology, University of California San Diego, La Jolla, California.
University of California, San Diego · USVA San Diego Healthcare System · USUniversity of Virginia · USLa Jolla Institute for Immunology · US

Funding

UC San Diego Clinical and Translational Research InstituteKL2TR001444 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEPP, COLIN A. · 2015 to 2024
$15.4M
The Role of the Adenosine Receptor in Th Cell Development and FunctionR01AI079145 · NIAID · UNIVERSITY OF VIRGINIA · PI ERNST, PETER B. · 2010 to 2022
$4.7M
Novel Traffic-targeted Therapies for IBDR01DK108670 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RIVERA-NIEVES, JESUS · 2016 to 2020
$3.3M
CyTOF Mass CytometerS10OD018499 · OD · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROTTY, SHANE P · 2014 to 2014
$802k
High Dimensional Mass Cytometry Analysis of the Effects of Vedolizumab in Intestinal Cellular Subsets and its Correlation with Clinical ParametersR21DK118927 · NIDDK · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI RIVERA-NIEVES, JESUS · 2019 to 2020
$392k
The Role of Adenosine Receptors in Th Cell Development and FunctionR56AI079145 · NIAID · UNIVERSITY OF VIRGINIA · PI ERNST, PETER B. · 2008 to 2008
$378k
Dendritic Cell Regulation by Sphingosine-1-phosphate in Inflammatory Bowel DiseaseI01BX003436 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI RIVERA-NIEVES, JESUS · 2019 to 2022
–
BLRD VA I01 BX003436NCATS NIH HHS KL2 TR001444NIAID NIH HHS R01 AI079145NIAID NIH HHS R56 AI079145NIDDK NIH HHS R01 DK108670NIDDK NIH HHS R21 DK118927NIH HHS S10 OD018499
6 · The paper itself

Abstract

Background: Novel therapeutics for inflammatory bowel disease (IBD) are under development, yet mechanistic readouts at the tissue level are lacking. Techniques to assess intestinal immune composition could represent a valuable tool for mechanism of action (MOA) studies of novel drugs. Mass cytometry enables analysis of intestinal inflammatory cell infiltrate and corresponding molecular fingerprints with unprecedented resolution. Here, we aimed to optimize the methodology for isolation and cryopreservation of cells from intestinal tissue to allow for the potential implementation of mass cytometry in MOA studies. Methods: We investigated key technical issues, including minimal tissue requirements, cell isolation protocols, and cell storage, using intestinal biopsies and peripheral blood from healthy individuals. High-dimensional mass cytometry was employed for the analyses of biopsy-derived intestinal cellular subsets. Results: Dithiothreitol and mechanical dissociation decreased epithelial cell contamination and allowed for isolation of adequate cell numbers from 2 to 4 colonic or ileal biopsies (6 × 104±2 × 104) after a 20-minute collagenase digestion, allowing for reliable detection of most major immune cell subsets. Biopsies and antibody-labeled mononuclear cells could be cryopreserved for later processing and acquisition (viability > 70%; P < 0.05). Conclusions: Mass cytometry represents a unique tool for deep immunophenotyping intestinal cell composition. This technique has the potential to facilitate analysis of drug actions at the target tissue by identifying specific cellular subsets and their molecular signatures. Its widespread implementation may impact not only IBD research but also other gastrointestinal conditions where inflammatory cells play a role in pathogenesis.

Indexed as

AgedCryopreservationEpithelial CellsFlow CytometryHumansImmunophenotypingInflammatory Bowel DiseasesIntestinal MucosaLeukocytes, MononuclearMass SpectrometryMiddle Aged

Identifiers

PMID29889233
PMCPMC6185553
OpenAlexW2805189782

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.