Evidence map›Paper›PMID 20921287›Full record

ArticleThe Journal of experimental medicine2010

A novel subset of CD4(+) T(H)2 memory/effector cells that produce inflammatory IL-17 cytokine and promote the exacerbation of chronic allergic asthma.

Yui-Hsi Wang, Kui Shin Voo, Bo Liu, Chun-Yu Chen, Burcin Uygungil, William Spoede, Jonathan A Bernstein, David P Huston, Yong-Jun Liu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 224 papers.

0numbers the graph read from it
0cells of the map it votes in
224citing papers in PubMed
12.8field-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.

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

224 citing papers in PubMed, 434 citations in OpenAlex.

  1. Trial
  2. A phenotypically and functionally distinct human TScience translational medicine · 2017
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  6. Article
  7. Article
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  13. Asthma Phenotypes and Biomarkers.Respiratory care · 2025
    Review
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  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

164 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

9 authors at 5 institutions in 2 countries.

Yui-Hsi WangDivision of Allergy and Immunology, University of Cincinnati, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. yui_hsi.wang@cchmc.org
Kui Shin Voo
Bo Liu
Chun-Yu Chen
Burcin Uygungil
William Spoede
Jonathan A Bernstein
David P Huston
Yong-Jun Liu
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · USGenomic (Brazil) · BRTexas A&M Health Science Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

TSLP Signaling in Dendritic Cells - Aim 3U19AI071130 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ZIEGLER, STEVEN F · 2006 to 2010
$6.1M
Regulation of TH2 memory/effector cells during allergic inflammationR01AI090129 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI WANG, YUI-HSI · 2010 to 2014
$1.9M
TSLP and Allergic InflammationR01AI061645 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIU, YONG-JUN · 2004 to 2008
$1.8M
NIAID NIH HHS R01 AI061645NIAID NIH HHS R01 AI061645-01NIAID NIH HHS R01 AI090129NIAID NIH HHS R01 AI090129-01NIAID NIH HHS U19 AI071130NIAID NIH HHS U19 AI071130-01
6 · The paper itself

Abstract

The inflammatory cytokine interleukin (IL)-17 is involved in the pathogenesis of allergic diseases. However, the identity and functions of IL-17-producing T cells during the pathogenesis of allergic diseases remain unclear. Here, we report a novel subset of T(H)2 memory/effector cells that coexpress the transcription factors GATA3 and RORγt and coproduce T(H)17 and T(H)2 cytokines. Classical T(H)2 memory/effector cells had the potential to produce IL-17 after stimulation with proinflammatory cytokines IL-1β, IL-6, and IL-21. The number of IL-17-T(H)2 cells was significantly increased in blood of patients with atopic asthma. In a mouse model of allergic lung diseases, IL-17-producing CD4(+) T(H)2 cells were induced in the inflamed lung and persisted as the dominant IL-17-producing T cell population during the chronic stage of asthma. Treating cultured bronchial epithelial cells with IL-17 plus T(H)2 cytokines induced strong up-regulation of chemokine eotaxin-3, Il8, Mip1b, and Groa gene expression. Compared with classical T(H)17 and T(H)2 cells, antigen-specific IL-17-producing T(H)2 cells induced a profound influx of heterogeneous inflammatory leukocytes and exacerbated asthma. Our findings highlight the plasticity of T(H)2 memory cells and suggest that IL-17-producing T(H)2 cells may represent the key pathogenic T(H)2 cells promoting the exacerbation of allergic asthma.

Indexed as

Immunologic MemoryAnimalsAsthmaChronic DiseaseCytokinesGATA3 Transcription FactorGene Expression RegulationHumansInterleukin-17Lymphocyte SubsetsMiceMice, Inbred BALB CNuclear Receptor Subfamily 1, Group F, Member 3Th2 CellsCytokinesGATA3 protein, humanGATA3 Transcription FactorInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3

Identifiers

PMID20921287
PMCPMC2964570
OpenAlexW2119636028

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.