Evidence map›Paper›PMID 41340286›Full record

ArticleThoracic research and practice2025

MSC-Exosomes as Novel Therapeutics in Asthma and Allergic Airway Inflammation.

Sevval Kurt, Ilgin Kimiz-Gebologlu, Suphi S Oncel

Abstract read
In one paragraph

Article in Thoracic research and practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. 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

3 authors.

Sevval KurtDepartment of Bioengineering, Faculty of Engineering, Ege University, Izmir, Türkiye.
Ilgin Kimiz-GebologluDepartment of Bioengineering, Faculty of Engineering, Ege University, Izmir, Türkiye.
Suphi S OncelDepartment of Bioengineering, Faculty of Engineering, Ege University, Izmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAllergic respiratory diseases, including asthma and allergic rhinitis, are chronic inflammatory diseases that affect millions of people worldwide and constitute a significant health problem.

conclusionPreclinical studies using both systemic and intranasal administration of MSC-Exos have demonstrated significant therapeutic benefits. In murine models of allergic airway inflammation, treatment with MSC-Exos resulted in reduced eosinophilic infiltration, decreased serum IgE levels, and suppression of mucus hypersecretion. These effects were accompanied by enhanced secretion of IL-10 and TGF-β, two key anti-inflammatory cytokines that contribute to an immunosuppressive microenvironment. Future Perspectives: MSC-Exos represent an innovative and safe therapeutic platform for allergic respiratory diseases such as asthma and rhinitis. By combining the regenerative and immunomodulatory properties of MSCs with the advantages of a cell-free system, they effectively regulate Th2 cytokines and restore immune balance. Future research should prioritize the scalable production and bioengineering optimization of MSC-Exos to enhance their stability, targeting efficiency, and bioactivity. Advances in exosome surface modification, such as ligand conjugation or genetic engineering of parent MSCs, may further improve selective delivery to inflamed airway tissues. Additionally, large-scale clinical trials are necessary to confirm therapeutic efficacy, establish optimal administration routes (e.g., intranasal vs. systemic), and ensure long-term safety. Beyond allergic airway diseases, the versatility of MSC-Exos may extend to other inflammatory and fibrotic lung conditions, including chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. As understanding of exosome biology deepens and bioengineering techniques advance, MSC-Exos are poised to become a cornerstone of next-generation immunomodulatory and regenerative therapies, bridging molecular biology, nanotechnology, and clinical immunology for transformative outcomes in respiratory medicine.

Indexed as

airway inflammationallergic diseasesexosomesimmunomodulatory therapyMesenchymal stem cell

Identifiers

PMID41340286
PMCPMC12673181

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.