Evidence map›Paper›PMID 30288751›Full record

ArticleAllergy2019

FoxO1 is a critical regulator of M2-like macrophage activation in allergic asthma.

Sangwoon Chung, Ji Y Kim, Min-Ae Song, Gye Y Park, Yong G Lee, Manjula Karpurapu, Joshua A Englert, Megan N Ballinger, Navjot Pabla, Hae Y Chung and 1 more

Abstract read
In one paragraph

Article in Allergy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Ethyl ferulate attenuates allergic asthma via inhibiting macrophage M2 polarization through STAT6/IRF4 pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Article
  3. Review
  4. MicroRNA clustering in pediatric asthma reveals differential corticosteroid responsiveness.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Article
  5. Article
  6. Article
  7. New mechanisms in diisocyanate-mediated allergy/toxicity: are microRNAs in play?Current opinion in allergy and clinical immunology · 2025
    Review
  8. Type 2 immunity in allergic diseases.Cellular & molecular immunology · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Canonical and non-canonical functions of NLRP3.Journal of advanced research · 2023
    Review
  13. Sex-specific lung inflammation and mitochondrial damage in a model of electronic cigarette exposure in asthma.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

11 authors at 4 institutions in 2 countries.

Sangwoon ChungPulmonary, Critical Care, and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart Lung Research Institute, Columbus, Ohio.ORCID 0000-0003-4484-8268
Ji Y KimDivision of Pharmaceutics, College of Pharmacy, The Ohio State University, Columbus, Ohio.
Min-Ae SongDivision of Environmental Health Sciences, College of Public Health, The Ohio State University, Columbus, Ohio.
Gye Y ParkPulmonary, Critical Care, Sleep and Allergy, University of Illinois at Chicago, Chicago, Illinois.
Yong G LeePulmonary, Critical Care, and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart Lung Research Institute, Columbus, Ohio.
Manjula KarpurapuPulmonary, Critical Care, and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart Lung Research Institute, Columbus, Ohio.
Joshua A EnglertPulmonary, Critical Care, and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart Lung Research Institute, Columbus, Ohio.
Megan N BallingerPulmonary, Critical Care, and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart Lung Research Institute, Columbus, Ohio.
Navjot PablaDivision of Pharmaceutics, College of Pharmacy, The Ohio State University, Columbus, Ohio.
Hae Y ChungDepartment of Pharmacy, College of Pharmacy, Pusan National University, Busan, Korea.
John W ChristmanPulmonary, Critical Care, and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart Lung Research Institute, Columbus, Ohio.
The Ohio State University Wexner Medical Center · USThe Ohio State University · USPusan National University · KRUniversity of Illinois Chicago · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Macrophage Gene Expression in Acute Lung InflammationR01HL075557 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHRISTMAN, JOHN W · 2004 to 2016
$4.8M
REGULATION OF THE MACROPHAGE INFLAMMATORY PHENOTYPE IN ARDSR01HL137224 · NHLBI · OHIO STATE UNIVERSITY · PI CHRISTMAN, JOHN W, KARPURAPU, MANJULA · 2018 to 2025
$4.5M
Role of alternatively activated macrophages in allergic asthmaR01HL126852 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PARK, GYE YOUNG · 2016 to 2020
$2.0M
NCI NIH HHS P30 CA016058NHLBI NIH HHS R01 HL075557NHLBI NIH HHS R01 HL126852NHLBI NIH HHS R01 HL137224
6 · The paper itself

Abstract

backgroundThe pathogenesis of asthma and airway obstruction is the result of an abnormal response to different environmental exposures. The scientific premise of our study was based on the finding that FoxO1 expression is increased in lung macrophages of mice after allergen exposure and human asthmatic patients. Macrophages are capable of switching from one functional phenotype to another, and it is important to understand the mechanisms involved in the transformation of macrophages and how their cellular function affects the peribronchial stromal microenvironment.

methodsWe employed a murine asthma model, in which mice were treated by intranasal insufflation with allergens for 2-8 weeks. We used both a pharmacologic approach using a highly specific FoxO1 inhibitor and genetic approaches using FoxO1 knockout mice (FoxO1

resultsWe show that the levels of FoxO1 gene are significantly elevated in the airway macrophages of patients with mild asthma in response to subsegmental bronchial allergen challenge. Transcription factor FoxO1 regulates a pro-asthmatic phenotype of lung macrophages that is involved in the development and progression of chronic allergic airway disease. We have shown that inhibition of FoxO1 induced phenotypic conversion of lung macrophages and downregulates pro-asthmatic and pro-fibrotic gene expression by macrophages, which contribute to airway inflammation and airway remodeling in allergic asthma.

conclusionTargeting FoxO1 with its downstream regulator IRF4 is a novel therapeutic target for controlling allergic inflammation and potentially reversing fibrotic airway remodeling.

Indexed as

Gene Expression Regulation, NeoplasticAdoptive TransferAllergensAnimalsAsthmaBronchial Provocation TestsBronchoscopyDisease Models, AnimalFemaleFlow CytometryForkhead Box Protein O1HumansMacrophage ActivationMacrophagesMiceTh2 CellsAllergensForkhead Box Protein O1FOXO1 protein, humanairway remodelingasthmatic inflammationFoxO1IRF4macrophages

Identifiers

PMID30288751
PMCPMC6393185
OpenAlexW2895001016

What OpenQuestion holds

Textmetadata
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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.