Evidence map›Paper›PMID 23945235›Full record

ArticleThe Journal of clinical investigation2013

Long-term IL-33-producing epithelial progenitor cells in chronic obstructive lung disease.

Derek E Byers, Jennifer Alexander-Brett, Anand C Patel, Eugene Agapov, Geoffrey Dang-Vu, Xiaohua Jin, Kangyun Wu, Yingjian You, Yael Alevy, Jean-Philippe Girard and 5 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 212 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed, 1 pooled it
11.2field-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

212 citing papers in PubMed, 1 synthesis or guideline pooled it, 326 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Emerging Systemic Treatments for Asthma and Allergic Diseases: New Tricks, Same Dog?The journal of allergy and clinical immunology. In practice · 2026
    Review
  10. Airway epithelial heterogeneity and mucus plugging in asthmatic bronchioles.American journal of respiratory and critical care medicine · 2026
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Tolerogenic lung allograft microenvironment suppresses pathogenic tissue remodeling following respiratory virus infection in mice.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  16. Article
  17. A translational view of airway epithelial dysfunction in COPD.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Derek E ByersDepartment of Medicine, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.
Jennifer Alexander-Brett
Anand C Patel
Eugene Agapov
Geoffrey Dang-Vu
Xiaohua Jin
Kangyun Wu
Yingjian You
Yael Alevy
Jean-Philippe Girard
Thaddeus S Stappenbeck
G Alexander Patterson
Richard A Pierce
Steven L Brody
Michael J Holtzman
Washington University in St. Louis · US

Funding

Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
VASCULAR CELL DIVERSITY IN PULMONARY HYPERTENSIONP01HL029594 · NHLBI · WASHINGTON UNIVERSITY · PI SHIPLEY, J MICHAEL · 1985 to 2012
$23.8M
Tissue and Cell Processing CoreU19AI070489 · NIAID · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2006 to 2016
$17.9M
PRINCIPLES IN PULMONARY RESEARCHT32HL007317 · NHLBI · WASHINGTON UNIVERSITY · PI Steven Brody, Michael J Holtzman · 1985 to 2026
$16.1M
Basis of Long-Term Virus-Induced Goblet Cell HyperplasiaR01HL073159 · NHLBI · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2003 to 2011
$3.1M
IL-33 AND EXCESS MUCUS PRODUCTIONR01HL121791 · NHLBI · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2014 to 2017
$1.9M
Target Validation and Assay Development for Anti-Mucus TherapyP50HL107183 · NHLBI · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2011 to 2012
$912k
Role of Calcium-Activated Chloride Channels in Airway Disease PhenotypesK08HL083095 · NHLBI · WASHINGTON UNIVERSITY · PI PATEL, ANAND CHAMPAK · 2007 to 2011
$600k
NCATS NIH HHS UL1 TR000448NHLBI NIH HHS K08 HL083095NHLBI NIH HHS K08-HL083095NHLBI NIH HHS P01 HL029594NHLBI NIH HHS P01-HL29594NHLBI NIH HHS P50 HL107183NHLBI NIH HHS P50-HL107183NHLBI NIH HHS R01 HL073159NHLBI NIH HHS R01-HL073159NHLBI NIH HHS R01 HL121791NHLBI NIH HHS T32 HL007317NIAID NIH HHS U19 AI070489NIAID NIH HHS U19-AI070489NIAID NIH HHS U54-AI05160
6 · The paper itself

Abstract

Chronic obstructive lung disease is characterized by persistent abnormalities in epithelial and immune cell function that are driven, at least in part, by infection. Analysis of parainfluenza virus infection in mice revealed an unexpected role for innate immune cells in IL-13-dependent chronic lung disease, but the upstream driver for the immune axis in this model and in humans with similar disease was undefined. We demonstrate here that lung levels of IL-33 are selectively increased in postviral mice with chronic obstructive lung disease and in humans with very severe chronic obstructive pulmonary disease (COPD). In the mouse model, IL-33/IL-33 receptor signaling was required for Il13 and mucin gene expression, and Il33 gene expression was localized to a virus-induced subset of airway serous cells and a constitutive subset of alveolar type 2 cells that are both linked conventionally to progenitor function. In humans with COPD, IL33 gene expression was also associated with IL13 and mucin gene expression, and IL33 induction was traceable to a subset of airway basal cells with increased capacities for pluripotency and ATP-regulated release of IL-33. Together, these findings provide a paradigm for the role of the innate immune system in chronic disease based on the influence of long-term epithelial progenitor cells programmed for excess IL-33 production.

Indexed as

AnimalsCase-Control StudiesCells, CulturedEpithelial CellsHumansImmunity, InnateInterleukin-1 Receptor-Like 1 ProteinInterleukin-33InterleukinsLungMaleMiceMice, Inbred C57BLMice, KnockoutPulmonary Disease, Chronic ObstructiveReceptors, InterleukinIl1rl1 protein, mouseIl33 protein, mouseInterleukin-1 Receptor-Like 1 ProteinInterleukin-33InterleukinsReceptors, Interleukin

Identifiers

PMID23945235
PMCPMC3754239
OpenAlexW2054599872

What OpenQuestion holds

Textmetadata
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.