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  2. New insights into allergic rhinitis treatment: MSC nanovesicles targeting dendritic cells

New insights into allergic rhinitis treatment: MSC nanovesicles targeting dendritic cells

  • J Nanobiotechnology. 2024 Sep 19;22(1):575. doi: 10.1186/s12951-024-02748-2.
Jianyu Liu 1 Meiqun Wang 1 Xiaoyan Tian 1 Shuhong Wu 1 Haisen Peng 1 Yaqiong Zhu 1 Yuehui Liu 2
Affiliations

Affiliations

  • 1 Department of Otolaryngology Head and Neck Surgery, Jiangxi Medical College, Nanchang University, No. 1, Minde Road, Nanchang, 330006, Jiangxi Province, China.
  • 2 Department of Otolaryngology Head and Neck Surgery, Jiangxi Medical College, Nanchang University, No. 1, Minde Road, Nanchang, 330006, Jiangxi Province, China. liuyuehuiclark@21cn.com.
Abstract

Allergic rhinitis (AR) is a condition with limited treatment options. This study investigates the potential use of mesenchymal stem cell (MSC) nanovesicles as a novel therapy for AR. Specifically, the study explores the underlying mechanisms of MSC nanovesicle therapy by targeting dendritic cells (DCs). The researchers fabricated DC-targeted P-D2-EVs nanovesicles and characterized their properties. Transcriptomic Sequencing and single-cell Sequencing analyses were performed to study the impact of P-D2-EVs on AR mice, identifying core genes involved in the treatment. In vitro cell experiments were conducted to validate the effects of P-D2-EVs on DC metabolism, Th2 differentiation, and ILC2 activation. The results showed that P-D2-EVs efficiently targeted DCs. Transcriptomic Sequencing analysis revealed differential expression of 948 genes in nasal tissue DCs of mice treated with P-D2-EVs. Single-cell Sequencing further revealed that P-D2-EVs had inhibitory effects on DC activation, Th2 differentiation, and ILC2 activation, with Fut1 identified as the core gene. Validation experiments demonstrated that P-D2-EVs improved IL10 metabolism in DCs by downregulating Fut1 expression, thereby suppressing Th2 differentiation and ILC2 activation. Animal experiments confirmed the inhibitory effects of P-D2-EVs and their ability to ameliorate AR symptoms in mice. The study suggests that P-D2-EVs reshape DC metabolism and suppress Th2 differentiation and ILC2 activation through the inhibition of the Fut1/ICAM1/p38 MAPK signaling pathway, providing a potential therapeutic approach for AR.

Keywords

Allergic rhinitis; Dendritic cells; Mesenchymal stem cells; Single-cell sequencing; T helper 2 cells; Type 2 innate lymphoid cells.

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