Evidence map›Paper›PMID 36177009›Full record

ArticleFrontiers in immunology2022

Human differentiated eosinophils release IL-13 in response to IL-33 stimulation.

Amiko M Uchida, Gabrielle Ro, Li Qiang, Kathryn A Peterson, June Round, Michael Dougan, Stephanie K Dougan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Cytokines in cancer.Cancer cell · 2025
    Review
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  7. Review
  8. Article
  9. Article
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  12. Article
  13. Review
  14. Role of CD34 in inflammatory bowel disease.Frontiers in physiology · 2023
    Review
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

7 authors at 3 institutions in 1 country.

Amiko M UchidaDivision of Gastroenterology, Hepatology and Nutrition, University of Utah, Salt Lake City, UT, United States.
Gabrielle RoDivision of Gastroenterology, Hepatology and Nutrition, University of Utah, Salt Lake City, UT, United States.
Li QiangCancer Immunology and Virology, Dana Farber Cancer Institute, Boston, MA, United States.
Kathryn A PetersonDivision of Gastroenterology, Hepatology and Nutrition, University of Utah, Salt Lake City, UT, United States.
June RoundDepartment of Pathology, University of Utah, Salt Lake City, Utah, United States.
Michael DouganCancer Immunology and Virology, Dana Farber Cancer Institute, Boston, MA, United States.
Stephanie K DouganCancer Immunology and Virology, Dana Farber Cancer Institute, Boston, MA, United States.
University of Utah · USDana-Farber Cancer Institute · USHarvard University · US

Funding

RESEARCH TRAINING IN DIGESTIVE DISEASES AND NUTRITIONT32DK007191 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1986 to 2026
$14.6M
Systematic interrogation of the pancreatic cancer microenvironment in patient-derived specimensU01CA224146 · NCI · DANA-FARBER CANCER INST · PI HAHN, WILLIAM C. · 2017 to 2021
$3.0M
CDK4/6 inhibition during CD8 T cell priming potentiates memory formation in mice and humansR01AI158488 · NIAID · DANA-FARBER CANCER INST · PI DOUGAN, STEPHANIE · 2021 to 2025
$2.2M
Regulation of brown fat metabolism by the immune receptor PD-L1K08DK114563 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI DOUGAN, MICHAEL LAWRENCE · 2017 to 2021
$868k
NCI NIH HHS U01 CA224146NIAID NIH HHS R01 AI158488NIDDK NIH HHS K08 DK114563NIDDK NIH HHS T32 DK007191
6 · The paper itself

Abstract

Objective: Eosinophils are hallmarks in allergic type 2 inflammation and are known to release cytotoxic granule proteins that contribute to inflammation. Eosinophils develop in the bone marrow from hematopoietic stem cells and once mature, have a limited lifespan in culture, making them difficult to study Methods: CD34+ and CD14+ cells were isolated from donor apheresis cones and differentiated into eosinophils or macrophage controls, respectively. Morphologic, transcriptional and protein analyses were performed to validate this method of eosinophil differentiation. The effect of IL-33 on differentiated eosinophils was assessed using qPCR, immunofluorescence, and multiplex cytokine array. Results: CD34 differentiated eosinophils appear morphologically similar by H&E and express eosinophil peroxidase (EPX) protein as well as the conventional eosinophil transcripts Conclusions: Our findings suggest that CD34 differentiated eosinophils are morphologically and phenotypically similar to peripheral eosinophils. The release of specific cytokines in direct response to IL-33 may contribute to the pathogenesis of type 2 inflammation and facilitates new avenues for studying eosinophils as effector cells

Indexed as

EosinophilsInterleukin-33Antigens, CD34CytokinesEosinophil PeroxidaseHumansInflammationInterleukin-13Interleukin-1 Receptor-Like 1 ProteinInterleukin-4Interleukin-8RNA, MessengerAntigens, CD34CytokinesEosinophil PeroxidaseInterleukin-13Interleukin-1 Receptor-Like 1 ProteinInterleukin-33Interleukin-4Interleukin-8RNA, MessengerallergyatopyCD34 cells+eosinophilic esophagitistype 2 inflammation

Identifiers

PMID36177009
PMCPMC9513478
OpenAlexW4295414700

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.