Evidence map›Paper›PMID 37259076›Full record

ArticleRespiratory research2023

Dysbiosis of the intestinal fungal microbiota increases lung resident group 2 innate lymphoid cells and is associated with enhanced asthma severity in mice and humans.

Amjad N Kanj, Theodore J Kottom, Kyle J Schaefbauer, Malay Choudhury, Andrew H Limper, Joseph H Skalski

Open access · goldAbstract readLetter
In one paragraph

Article in Respiratory research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  9. The role of dietary fibre in lung inflammation: microbiota, metabolites, and immune crosstalk.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Journal of fungi (Basel, Switzerland) · 2025
    Review
  14. Review
  15. Type 2 immunity in allergic diseases.Cellular & molecular immunology · 2025
    Review
  16. Review
  17. Article
  18. Respiratory diseases and the gut microbiota: an updated review.Frontiers in cellular and infection microbiology · 2025
    Review
  19. Article
  20. Article
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

6 authors at 2 institutions in 1 country.

Amjad N KanjDivision of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, USA.
Theodore J KottomThoracic Disease Research Unit, Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Kyle J SchaefbauerThoracic Disease Research Unit, Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Malay ChoudhuryThoracic Disease Research Unit, Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Andrew H LimperDivision of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, USA.
Joseph H SkalskiDivision of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, USA. Skalski.Joseph@mayo.edu.
Mayo Clinic · USMayo Clinic in Florida · US

Funding

Interdisciplinary Training in Lung Physiology and Biomedical EngineeringT32HL105355 · NHLBI · MAYO CLINIC ROCHESTER · PI PRAKASH, Y. S., SIECK, GARY C. · 2012 to 2021
$3.9M
Targeting the Amino Acid Transporter SLC7A5 for Pulmonary FibrosisR01HL167732 · NHLBI · WASHINGTON UNIVERSITY · PI Malay Choudhury · 2023 to 2026
$2.0M
Targeting the Amino Acid Transporter SLC7A5 for Treatment of Pulmonary FibrosisR56HL158549 · NHLBI · WASHINGTON UNIVERSITY · PI CHOUDHURY, MALAY · 2022 to 2022
$397k
NHLBI NIH HHS R01 HL167732NHLBI NIH HHS R56 HL158549NIH HHS T32 HL105355
6 · The paper itself

Abstract

backgroundThe gut-lung axis is the concept that alterations of gut microbiota communities can influence immune function in the lungs. While studies have explored the relationship between intestinal bacterial dysbiosis and asthma development, less is understood about the impact of commensal intestinal fungi on asthma severity and control and underlying mechanisms by which this occurs.

methodsWild-type mice were treated with Cefoperazone to deplete gut bacteria and administered Candida albicans or water through gavage. Mice were then sensitized to house dust mite (HDM) and their lungs were analyzed for changes in immune response. Humans with asthma were recruited and stool samples were analyzed for Candida abundance and associations with asthma severity and control.

resultsMice with intestinal Candida dysbiosis had enhanced Th2 response after airway sensitization with HDM, manifesting with greater total white cell and eosinophil counts in the airway, and total IgE concentrations in the serum. Group 2 innate lymphoid cells (ILC2) were more abundant in the lungs of mice with Candida gut dysbiosis, even when not sensitized to HDM, suggesting that ILC2 may be important mediators of the enhanced Th2 response. These effects occurred with no detectable increased Candida in the lung by culture or rtPCR suggesting gut-lung axis interactions were responsible. In humans with asthma, enhanced intestinal Candida burden was associated with the risk of severe asthma exacerbation in the past year, independent of systemic antibiotic and glucocorticoid use.

conclusionsCandida gut dysbiosis may worsen asthma control and enhance allergic airway inflammation, potentially mediated by ILC2. Further studies are necessary to examine whether microbial dysbiosis can drive difficult-to-control asthma in humans and to better understand the underlying mechanisms.

Indexed as

AsthmaGastrointestinal MicrobiomeMycobiomeAnimalsDisease Models, AnimalDysbiosisHumansImmunity, InnateLungLymphocytesMicePyroglyphidaeAsthmaCandidaGutILC2Mycobiota

Identifiers

PMID37259076
PMCPMC10230676
OpenAlexW4378904480

What OpenQuestion holds

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LicenceCC BY
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.