Evidence map›Paper›PMID 24890729›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2014

IL-1β promotes the differentiation of polyfunctional human CCR6+CXCR3+ Th1/17 cells that are specific for pathogenic and commensal microbes.

Thomas Duhen, Daniel J Campbell

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

78 citing papers in PubMed, 128 citations in OpenAlex.

  1. Review
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  6. Article
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  11. IL-23 Promotes γδT Cell Activity in Dry Eye Disease Progression.Investigative ophthalmology & visual science · 2025
    Article
  12. Review
  13. Review
  14. Review
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  16. Article
  17. MDR1-EXPRESSING CD4Journal for immunotherapy of cancer · 2023
    Article
  18. Article
  19. Article
  20. Article

18 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

2 authors at 1 institution in 1 country.

Thomas DuhenImmunology Program, Benaroya Research Institute, Seattle, WA 98101; andDepartment of Immunology, University of Washington School of Medicine, Seattle, WA 98195.
Daniel J CampbellImmunology Program, Benaroya Research Institute, Seattle, WA 98101; andDepartment of Immunology, University of Washington School of Medicine, Seattle, WA 98195 campbell@benaroyaresearch.org.
Behavioral Tech Research, Inc. · US

Funding

Thymic Stromal Lymphopoietin (TSLP) and Lung Inflammation and ImmP01HL098067 · NHLBI · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI FREVERT, CHARLES WAYNE · 2010 to 2014
$13.5M
Homing and Homeostasis of Regulatory T cellsR01AI067750 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2006 to 2010
$2.6M
Regulation of TSLP-Mediated Skin InflammationR01AR055695 · NIAMS · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J, HAMERMAN, JESSICA A · 2009 to 2013
$2.0M
Homing and function of regulatory T cells specific for islet antigensR01DK072295 · NIDDK · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2005 to 2009
$1.6M
Homing and Homeostasis of Regulatory T cellsR56AI067750 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2012 to 2012
$427k
NHLBI NIH HHS HL098067NHLBI NIH HHS P01 HL098067NIAID NIH HHS AI067750NIAID NIH HHS R01 AI067750NIAID NIH HHS R56 AI067750NIAMS NIH HHS AR055695NIAMS NIH HHS R01 AR055695NIDDK NIH HHS DK072295NIDDK NIH HHS R01 DK072295
6 · The paper itself

Abstract

In humans, Th1/17 cells, identified by coexpression of the chemokine receptors CCR6 and CXCR3, are proposed to be highly pathogenic in several autoimmune disorders due in part to their expression of the proinflammatory cytokines IL-17, IFN-γ, and GM-CSF. However, their developmental requirements, relationship with "classic" Th17 and Th1 cells and physiological role in normal immune responses are not well understood. In this study, we examined CCR6+ CXCR3+ Th1/17 cells from healthy individuals and found that ex vivo these cells produced the effector cytokines IL-17, IL-22, and IFN-γ in all possible combinations and were highly responsive to both IL-12 and IL-23. Moreover, although the Ag specificity of CCR6+ CXCR3+ Th1/17 cells showed substantial overlap with that of Th1 and Th17 cells, this population was enriched in cells recognizing certain extracellular bacteria and expressing the intestinal homing receptor integrin β7. Finally, we identified IL-1β as a key cytokine that renders Th17 cells sensitive to IL-12, and both cytokines together potently induced the differentiation of cells that produce IL-17, IFN-γ, and GM-CSF. Therefore, interfering with IL-1β and IL-12 signaling in Th17 cells during inflammation may be a promising therapeutic approach to reduce their differentiation into "pathogenic" CCR6+ CXCR3+ Th1/17 cells in patients with autoimmune diseases.

Indexed as

BacteriaCell DifferentiationCytokinesFemaleHumansInterleukin-1betaMaleReceptors, CCR6Receptors, CXCR3Th17 CellsTh1 CellsCCR6 protein, humanCXCR3 protein, humanCytokinesIL1B protein, humanInterleukin-1betaReceptors, CCR6Receptors, CXCR3

Identifiers

PMID24890729
PMCPMC4068296
OpenAlexW1641463952

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.