Volume 49, Issue 2 pp. 227-238
ORIGINAL ARTICLE

Role of house dust mite-derived extracellular vesicles in a murine model of airway inflammation

Jun-Pyo Choi

Jun-Pyo Choi

Division of Allergy and Clinical Immunology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

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Seong Gyu Jeon

Seong Gyu Jeon

Research Institute, AEON Medix, Inc, Pohang, Korea

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Yoon-Keun Kim

Yoon-Keun Kim

MD Healthcare, Inc, Seoul, Korea

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You Sook Cho

Corresponding Author

You Sook Cho

Division of Allergy and Clinical Immunology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Correspondence

You Sook Cho, Division of Allergy and Clinical Immunology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Email: [email protected]

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First published: 12 October 2018
Citations: 12

Funding information

This study was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health and Welfare, Republic of Korea (grant number: HI14C2628).

Summary

Background

House dust mite (HDM) is the major source of indoor allergens that cause airway disease. Recent evidence suggests that Gram-negative/positive bacteria produce nano-sized extracellular vesicles (EVs) containing diverse components, including various immunostimulatory molecules. However, the association between bacteria-derived EVs and development of airway disease is unclear.

Objective

To identify and isolate HDM-derived EVs and to evaluate their effect on the development of airway inflammation.

Methods

Extracellular vesicles were isolated from crude HDM extracts by ultra-centrifugation, and their physical and immunological characteristics and roles in airway inflammation were tested in vitro and in murine models of airway inflammation. In addition, 16s metagenome analysis of nucleic acid from EVs was performed to identify their origin.

Results

Round, bilayered vesicles measuring 80-100 nanometres and containing abundant amounts of LPS were isolated. These vesicles induced innate immune responses both in vitro and in vivo. Intranasal exposure of naïve mice to HDM EVs induced production of cytokines associated with development of Th2-mediated and mixed (Th1-/Th2-/Th17-mediated) airway inflammation to allergen. Metagenome analysis identified Bacteroidetes and Proteobacteria as the probable sources of HDM EVs.

Conclusion

House dust mite EVs originating from Gram-negative bacteria may play an important role on the development of airway inflammation.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

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