Evidence map›Paper›PMID 31437129›Full record

ArticleThe Journal of clinical investigation2019

Airway epithelium-shifted mast cell infiltration regulates asthmatic inflammation via IL-33 signaling.

Matthew C Altman, Ying Lai, James D Nolin, Sydney Long, Chien-Chang Chen, Adrian M Piliponsky, William A Altemeier, Megan Larmore, Charles W Frevert, Michael S Mulligan and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

64 citing papers in PubMed, 100 citations in OpenAlex.

  1. Trial
  2. Developments in Mast Cell Research.The Journal of allergy and clinical immunology · 2026
    Review
  3. Mast cell-derived extracellular vesicles in lung diseases: roles in pulmonary inflammation, immune regulation, and microenvironmental remodeling.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. The immunology of asthma.Nature immunology · 2025
    Review
  13. Article
  14. Review
  15. Clinical and Biological Features of a Thickened Basement Membrane Zone in Asthma.American journal of respiratory and critical care medicine · 2025
    Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Article

4 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

14 authors at 4 institutions in 1 country.

Matthew C AltmanDivision of Allergy and Infectious Diseases and.
Ying LaiDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA.
James D NolinDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA.
Sydney LongDivision of Allergy and Infectious Diseases and.
Chien-Chang ChenDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA.
Adrian M PiliponskyCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, Washington, USA.
William A AltemeierDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA.
Megan LarmoreDepartment of Comparative Medicine, University of Washington, Seattle, Washington, USA.
Charles W FrevertDepartment of Comparative Medicine, University of Washington, Seattle, Washington, USA.
Michael S MulliganDivision of Cardiothoracic Surgery, Department of Surgery, University of Washington, Seattle, Washington, USA.
Steven F ZieglerImmunology Program, Benaroya Research Institute, Seattle, Washington, USA.
Jason S DebleyCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, Washington, USA.
Michael C PetersDivision of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, UCSF, San Francisco, California, USA.
Teal S HallstrandDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA.
University of Washington · USSeattle Children's Hospital · USBenaroya Research InstitutePulmonary and Allergy Associates · US

Funding

Regulation of the Innate Immune Response by the Epithelium in AsthmaU19AI125378 · NIAID · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI CAMPBELL, DANIEL J · 2016 to 2020
$9.2M
Secretory Phospholipase A2s in Airway PathophysiologyR01HL089215 · NHLBI · UNIVERSITY OF WASHINGTON · PI HALLSTRAND, TEAL S · 2008 to 2017
$4.0M
Regulation of Allergen-Induced Airway Pathophysiology by VersicanR01AI130280 · NIAID · UNIVERSITY OF WASHINGTON · PI FREVERT, CHARLES WAYNE, HALLSTRAND, TEAL S · 2019 to 2023
$3.8M
Origin and Function of Intra-epithelial Mast Cells in AsthmaR01HL153979 · NHLBI · UNIVERSITY OF WASHINGTON · PI HALLSTRAND, TEAL S · 2021 to 2024
$2.9M
Dysregulated Airway Epithelial Signaling as a Driver of Airway Remodeling in Asthmatic ChildrenR01HL128361 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI DEBLEY, JASON S · 2016 to 2018
$1.4M
Immunopathology of Indirect Airway Hyperresponsiveness in AsthmaK24AI130263 · NIAID · UNIVERSITY OF WASHINGTON · PI Teal S Hallstrand · 2017 to 2026
$1.3M
Uncovering Biologic Mechanisms of Severe AsthmaK23HL138303 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PETERS, MICHAEL · 2017 to 2020
$709k
Secreted Phospholipase A2 Group X Regulation of Type-2 InflammationF32HL134217 · NHLBI · UNIVERSITY OF WASHINGTON · PI NOLIN, JAMES D · 2017 to 2018
$90k
EPA R835738NHLBI NIH HHS F32 HL134217NHLBI NIH HHS K23 HL138303NHLBI NIH HHS R01 HL089215NHLBI NIH HHS R01 HL128361NHLBI NIH HHS R01 HL153979NIAID NIH HHS K24 AI130263NIAID NIH HHS R01 AI130280NIAID NIH HHS U19 AI125378
6 · The paper itself

Abstract

Asthma is a heterogeneous syndrome that has been subdivided into physiologic phenotypes and molecular endotypes. The most specific phenotypic manifestation of asthma is indirect airway hyperresponsiveness (AHR), and a prominent molecular endotype is the presence of type 2 inflammation. The underlying basis for type 2 inflammation and its relationship to AHR are incompletely understood. We assessed the expression of type 2 cytokines in the airways of subjects with and without asthma who were extensively characterized for AHR. Using quantitative morphometry of the airway wall, we identified a shift in mast cells from the submucosa to the airway epithelium specifically associated with both type 2 inflammation and indirect AHR. Using ex vivo modeling of primary airway epithelial cells in organotypic coculture with mast cells, we show that epithelial-derived IL-33 uniquely induced type 2 cytokines in mast cells, which regulated the expression of epithelial IL33 in a feed-forward loop. This feed-forward loop was accentuated in epithelial cells derived from subjects with asthma. These results demonstrate that type 2 inflammation and indirect AHR in asthma are related to a shift in mast cell infiltration to the airway epithelium, and that mast cells cooperate with epithelial cells through IL-33 signaling to regulate type 2 inflammation.

Indexed as

AsthmaFemaleHumansInflammationInterleukin-33MaleMast CellsRespiratory MucosaSignal TransductionIL33 protein, humanInterleukin-33AsthmaImmunologyMast cellsPulmonologyTh2 response

Identifiers

PMID31437129
PMCPMC6819127
OpenAlexW2969359130

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.