Evidence map›Paper›PMID 32428507›Full record

Observational studyGastroenterology2020

Single-Cell Analyses of Colon and Blood Reveal Distinct Immune Cell Signatures of Ulcerative Colitis and Crohn's Disease.

Vanessa Mitsialis, Sarah Wall, Peng Liu, Jose Ordovas-Montanes, Tamar Parmet, Marko Vukovic, Dennis Spencer, Michael Field, Collin McCourt, Jessica Toothaker and 10 more

Registry-linked trialOpen access · greenAbstract readObservational Study
In one paragraph

Observational study in Gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04508088 (Skeletal Health and Bone Marrow Composition in Newly Diagnosed Adolescents With Crohn Disease), which is not on this map. Cited by 235 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
235citing papers in PubMed, 4 pooled it
27.7field-weighted citation impact, top 1% 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.

NCT04508088 recruitingnot on this map

Skeletal Health and Bone Marrow Composition in Newly Diagnosed Adolescents With Crohn Disease

TypeobservationalSponsorMassachusetts General HospitalRan2020 to 2026Enrolled92ConditionsInflammatory Bowel Disease, Crohn DiseaseArmsCoronal T1 weighted spin echo images, Spin-lattice relaxation (T1), Magnetic resonance spectroscopy, Blood Draw
3 · Its place in the literature

Who cites it

235 citing papers in PubMed, 4 syntheses or guidelines pooled it, 332 citations in OpenAlex.

  1. Pooled it
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  5. Article
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  7. Changes in leukocytes and CRP in different treatments of major depression.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Article
  8. NADAging cell · 2026
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  13. DNA From Neutrophil Extracellular Traps Restricts Group 3 Innate Lymphoid Cells Function in Intestinal Epithelial Repair via CCDC25.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  14. Article
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  17. Regulatory T cells in cancer and inflammation.Signal transduction and targeted therapy · 2026
    Review
  18. The roles and heterogeneity of CD8International journal of molecular medicine · 2026
    Review
  19. Article
  20. Article

175 more citing papers are in PubMed but not listed here.

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

20 authors at 7 institutions in 1 country.

Vanessa MitsialisDivision of Gastroenterology, Brigham and Women's Hospital, Boston, Massachusetts; Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Sarah WallDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Peng LiuDepartment of Biostatistics University of Pittsburgh, Pittsburgh, Pennsylvania.
Jose Ordovas-MontanesDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts; Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts; Harvard Stem Cell Institute, Cambridge, Massachusetts.
Tamar ParmetDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Marko VukovicBroad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts; Harvard Stem Cell Institute, Cambridge, Massachusetts; Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, Massachusetts; Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts; Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts.
Dennis SpencerDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Michael FieldDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Collin McCourtBroad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts.
Jessica ToothakerHarvard Stem Cell Institute, Cambridge, Massachusetts.
Athos BousvarosDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Boston Children’s Hospital Inflammatory Bowel Disease Center
Brigham and Women’s Hospital Crohn’s and Colitis Center
Alex K ShalekBroad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts; Harvard Stem Cell Institute, Cambridge, Massachusetts; Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, Massachusetts; Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts; Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts.
Leslie KeanDivision of Hematology Oncology, Boston Children's Hospital, Boston, Massachusetts.
Bruce HorwitzDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.
Jeffrey GoldsmithDepartment of Pathology, Boston Children's Hospital, Boston, Massachusetts.
George TsengDepartment of Biostatistics University of Pittsburgh, Pittsburgh, Pennsylvania.
Scott B SnapperDivision of Gastroenterology, Brigham and Women's Hospital, Boston, Massachusetts; Division of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, Massachusetts. Electronic address: scott.snapper@childrens.harvard.edu.
Liza KonnikovaDivision of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts; Department of Pediatrics, University of Pittsburgh Medical Center Children's Hospital, Pittsburgh, Pennsylvania; Department of Immunology, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Developmental Biology University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut. Electronic address: Liza.konnikova@chp.edu.
Boston Children's Hospital · USBroad Institute · USBrigham and Women's Hospital · USUniversity of Pittsburgh · USChildren's Hospital of Pittsburgh · USHarvard Stem Cell Institute · USRagon Institute of MGH, MIT and Harvard · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Autoimmunity and Immunopathology Training ProgramT32AI089443 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SHLOMCHIK, MARK J · 2010 to 2024
$6.6M
Type III interferon Control of Mucosal ImmunityR01DK115217 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI Scott B Snapper, Ivan Zanoni · 2017 to 2026
$5.6M
ALIMENTARY TRACT RESEARCH IN HEALTH AND DISEASET32DK007533 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BLUMBERG, RICHARD S · 1986 to 2020
$5.3M
An integrated multiplexed genomic assay for low input clinical samples1U24AI118672 · NIAID · BROAD INSTITUTE, INC. · PI SHALEK, ALEX K · 2015 to 2019
$2.0M
Employing novel humanized murine strains to develop hematopoietic stem cell gene therapeutic approaches for very early-onset inflammatory bowel disease due to IL10-receptor deficiency.R56AI125766 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI SNAPPER, SCOTT B, WILLIAMS, DAVID A · 2017 to 2017
$408k
Howard Hughes Medical Institute DRG-2274-16NCATS NIH HHS UL1 TR001863NIAID NIH HHS R56 AI125766NIAID NIH HHS T32 AI089443NIAID NIH HHS U24 AI118672NIDDK NIH HHS P30 DK034854NIDDK NIH HHS R01 DK115217NIDDK NIH HHS T32 DK007533
6 · The paper itself

Abstract

BACKGROUND &

aimsStudies are needed to determine the mechanisms of mucosal dysregulation in patients with inflammatory bowel diseases (IBDs) and differences in inflammatory responses of patients with ulcerative colitis (UC) vs Crohn's disease (CD). We used mass cytometry (CyTOF) to characterize and compare immune cell populations in the mucosa and blood from patients with IBD and without IBD (controls) at single-cell resolution.

methodsWe performed CyTOF analysis of colonic mucosa samples (n = 87) and peripheral blood mononuclear cells (n = 85) from patients with active or inactive UC or CD and controls. We also performed single-cell RNA sequencing, flow cytometry, and RNA in situ hybridization analyses to validate key findings. We used random forest modeling to identify differences in signatures across subject groups.

resultsCompared with controls, colonic mucosa samples from patients with IBD had increased abundances of HLA-DR+CD38+ T cells, including T-regulatory cells that produce inflammatory cytokines; CXCR3+ plasmablasts; and IL1B+ macrophages and monocytes. Colonic mucosa samples from patients with UC were characterized by expansion of IL17A+ CD161+ effector memory T cells and IL17A+ T-regulatory cells; expansion of HLA-DR+CD56+ granulocytes; and reductions in type 3 innate lymphoid cells. Mucosal samples from patients with active CD were characterized by IL1B+HLA-DR+CD38+ T cells, IL1B+TNF+IFNG

conclusionsWe used single-cell technologies to identify immune cell populations specific to mucosa and blood samples from patients with active or inactive CD and UC and controls. This information might be used to develop therapies that target specific cell populations in patients with different types of IBD.

Indexed as

Immunity, CellularAdolescentAdultCase-Control StudiesChildColitis, UlcerativeColonCrohn DiseaseFemaleFlow CytometryHumansImmunophenotypingIntestinal MucosaMaleRNA-SeqSingle-Cell AnalysisILC3MAIT CellsscRNA-SeqTreg

Identifiers

PMID32428507
PMCPMC8166295
OpenAlexW3024444185

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Registered trials

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.