Evidence map›Paper›PMID 32197970›Full record

ArticleThe Journal of allergy and clinical immunology2020

Esophageal type 2 cytokine expression heterogeneity in eosinophilic esophagitis in a multisite cohort.

Julia L M Dunn, Tetsuo Shoda, Julie M Caldwell, Ting Wen, Seema S Aceves, Margaret H Collins, Evan S Dellon, Gary W Falk, John Leung, Lisa J Martin and 8 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
7.4field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

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  5. Eosinophilic gastrointestinal diseases.Nature reviews. Disease primers · 2026
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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

18 authors at 12 institutions in 1 country.

Julia L M DunnDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Tetsuo ShodaDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Julie M CaldwellDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Ting WenDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Seema S AcevesDivision of Allergy Immunology, University of California, San Diego, Calif; Rady Children's Hospital, San Diego, Calif.
Margaret H CollinsDivision of Pathology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati.
Evan S DellonCenter for Esophageal Diseases and Swallowing and Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC.
Gary W FalkDivision of Gastroenterology, Hospital of the University of Pennsylvania, Philadelphia, Pa.
John LeungDivision of Gastroenterology, Tufts Medical Center, Boston, Mass.
Lisa J MartinDivision of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, Ohio.
Paul Menard-KatcherDivision of Gastroenterology & Hepatology, University of Colorado Anschutz Medical Campus, Aurora, Colo.
Amanda K Rudman-SpergelAllergy, Asthma and Airway Biology Branch Division of Allergy, Immunology and Transplantation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Md.
Jonathan M SpergelDivision of Allergy and Immunology, Children's Hospital of Philadelphia, School of Medicine, University of Pennsylvania, Philadelphia, Pa.
Joshua B WechslerDivision of Gastroenterology, Hepatology and Nutrition, Lurie Children's Hospital of Chicago, Chicago, Ill.
Guang-Yu YangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Glenn T FurutaDigestive Health Institute, Children's Hospital Colorado, Gastrointestinal Eosinophilic Diseases Program, University of Colorado School of Medicine, Aurora, Colo.
Marc E RothenbergDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio. Electronic address: Rothenberg@cchmc.org.
Consortium of Eosinophilic Gastrointestinal Disease Researchers (CEGIR)
University of Cincinnati · USCincinnati Children's Hospital Medical Center · USHospital of the University of Pennsylvania · USLurie Children's Hospital · USNational Institutes of Health · USNorthwestern University · USRady Children's Hospital-San Diego · USTufts Medical Center · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Colorado Denver · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Alexander Miethke · 2007 to 2026
$24.4M
TRAINING (CAREER DEVELOPMENT) COMPONENTU54AI117804 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI GLENN T FURUTA, Marc E. Rothenberg · 2014 to 2026
$18.5M
NIAID NIH HHS U54 AI117804NIDDK NIH HHS P30 DK078392
6 · The paper itself

Abstract

backgroundThere is strong evidence for a role of type 2 cytokines in the pathogenesis of eosinophilic esophagitis (EoE); however, heterogeneity in type 2 gene expression has not been examined.

objectiveWe examined type 2 immunity-associated gene expression in esophageal biopsy specimens, aiming to determine the degree of cytokine heterogeneity and its potential clinical significance.

methodsPatients (n = 312) were recruited from 10 sites associated with the Consortium of Eosinophilic Gastrointestinal Disease Researchers. In addition to histologic and endoscopic assessment, esophageal biopsy specimens were examined for expression of 96 genes within the EoE diagnostic panel.

resultsFive subgroups of patients with active EoE were identified by unsupervised clustering based on expression of IL4, IL5, IL13, C-C motif chemokine ligand 26 (CCL26), thymic stromal lymphopoietin (TSLP), Charcot-Leyden crystal (CLC), C-C motif chemokine receptor 3 (CCR3), and CPA3. These groups differed in age (P < .02) and EoE diagnostic panel score (P < 1.08E-30) but not in eosinophil levels. The group V patients had the highest expression of IL5, TSLP, and CCL26 and genes associated with tissue remodeling, such as COL8A1, actin γ-2 (ACTG2), and tetraspanin 12 (TSPAN12). IL5 and IL13 were highly expressed in group IV; however, groups IV and V differed in age (34 vs 14 years [P < .05]). Groups II and III, which exhibited intermediate expression of IL5 and CPA3, were differentiated by high TSLP and IL13 in group III.

conclusionWe observed heterogeneous type 2 gene expression among patients with active EoE. Type 2 gene overexpression was not directly proportional to disease features; this was especially true for tissue remodeling events. These findings highlight a clinical opportunity for leveraging molecular endotypes to implement personalized medicine in EoE.

Indexed as

AdolescentAdultAgedChildCohort StudiesCytokinesEosinophilic EsophagitisEosinophilsEsophagusFemaleGene ExpressionHumansMaleMiddle AgedCytokinesAllergycytokineeosinophilfibrosisIL-13IL-5inflammationprecision medicineresolutionT(H)2 cells

Identifiers

PMID32197970
PMCPMC7309223
OpenAlexW3012207862

What OpenQuestion holds

Textmetadata
LicenceTDM
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.