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A20-OVA Nanoparticles Inhibit Allergic Asthma in a Murine Model.
- Source :
-
Inflammation [Inflammation] 2020 Jun; Vol. 43 (3), pp. 953-961. - Publication Year :
- 2020
-
Abstract
- The skewed T helper (Th) 2 response plays a critical role in the pathogenesis of allergic asthma. Regulatory T (Treg) cells and the regulatory cytokines are required in maintaining the homeostasis in the body. This study aims to determine the effects of a poly(lactic-co-glycolic) acid (PLGA)-ovalbumin (OVA)+A20 (a ubiquitin E3 ligase) nanovaccine on inhibiting allergic asthma in a murine model. In this study, A20 and OVA (a model antigen) were encapsulated into PLGA to be a nanovaccine (PLGA-OVA+A20). An allergic asthma murine model was developed with OVA as the specific antigen to test the role of PLGA-OVA+A20 nanovaccine in maintaining the immune homeostasis in the airway tissues. The results showed that PLGA-OVA+A20 nanovaccine inhibited the asthma responses in mice by suppressing Th2 inflammatory responses, promoting the generation of Treg cells in the airway tissues. We conclude that the PLGA-OVA+A20 nanovaccine has a marked inhibitory effect on the airway allergic response in sensitized mice by significantly promoting the generation of Treg cell and IL-10. The data suggest that PLGA-OVA+A20 has translational potential in the treatment of allergic asthma.
- Subjects :
- Animals
Asthma immunology
Asthma metabolism
Dose-Response Relationship, Drug
Female
Mice
Mice, Inbred BALB C
T-Lymphocytes, Regulatory drug effects
T-Lymphocytes, Regulatory immunology
T-Lymphocytes, Regulatory metabolism
Asthma prevention & control
Disease Models, Animal
Nanoparticles administration & dosage
Ovalbumin administration & dosage
Polylactic Acid-Polyglycolic Acid Copolymer administration & dosage
Tumor Necrosis Factor alpha-Induced Protein 3 administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1573-2576
- Volume :
- 43
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Inflammation
- Publication Type :
- Academic Journal
- Accession number :
- 31938979
- Full Text :
- https://doi.org/10.1007/s10753-020-01181-5