| Literature DB >> 31938979 |
Xiang-Qian Luo1, Jian-Wen Zhong1, Shu-Yao Qiu1, Min Zhi1, Li-Qiang Yang1, Yi-Long Zhou1, Fen-Xuan Zhou1, Ping-Chang Yang2, Da-Bo Liu1, Li-Hua Mo3.
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.Entities:
Keywords: A20; Th2 response; allergic asthma; nanovaccine; regulatory T cell
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Year: 2020 PMID: 31938979 DOI: 10.1007/s10753-020-01181-5
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092