致命的な肺疾患に対するバイオミメティック治療法を開発(Scientists Develop Biomimetic Therapy for Fatal Lung Disease)

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2025-06-24 中国科学院(CAS)

致命的な肺疾患に対するバイオミメティック治療法を開発(Scientists Develop Biomimetic Therapy for Fatal Lung Disease)BEV-SNA-mediated therapy for idiopathic pulmonary fibrosis. (Image by NIMTE)

中国科学院寧波材料技術・工学研究所(NIMTE)などの研究チームは、難治性の特発性肺線維症(IPF)治療に有望な新しいナノ治療法「BEV-SNA(バイオミメティック細胞外小胞スフェリカル核酸)」を開発しました。これは間葉系幹細胞由来の細胞外小胞(MSC-EV)を基に、コレステロール修飾DNAを加えて3次元構造を形成し、肺組織への浸透性を大幅に高めたものです。BEV-SNAは、自然なEVと比べて17.2倍の生産性を実現し、マウス実験ではROS除去・炎症抑制・線維化防止などで優れた効果を示しました。生存率も50%に改善され、既存治療薬より高い有効性が期待されます。本研究は、呼吸器疾患の革新的治療やバイオミメティックナノ医療の発展に貢献する可能性があります。

<関連情報>

活性酸素消去および抗炎症作用による肺線維症治療のための肺透過性バイオミメティック細胞外小胞球状核酸 Lung-Penetrating Biomimetic Extracellular Vesicle Spherical Nucleic Acids for Pulmonary Fibrosis Therapy Through ROS Scavenging and Anti-Inflammatory Effects

Saiyun Lou, Jiangpo Ma, Pan Fu, Lin Li, Jingyun Huang, Fangxue Jing, Yuhui Wang, Sihua Qian, Jianping Zheng, Jiang Li, Zhaoxing Dong, Kaizhe Wang
Aggregate  Published: 12 June 2025
DOI:https://doi.org/10.1002/agt2.70086

ABSTRACT

Idiopathic pulmonary fibrosis (IPF) is an irreversible and fatal lung disease characterized by persistent alveolar epithelial cell injury and extracellular matrix deposition. Early dual modulation of oxidative stress and inflammation may offer a promising therapeutic opportunity. Mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) offer therapeutic promise but face challenges in scalability and efficient lung delivery. Here, we developed a biomimetic extracellular vesicle-spherical nucleic acid (BEV-SNA) platform for IPF therapy. BEV-SNA were constructed by integrating mechanically extruded BEVs from primary MSCs with cholesterol-modified ssDNA through hydrophobic co-assembly. In stemness-maintained P0-P1 MSCs, the production of BEVs increased by 17.2-fold compared to natural EVs. Benefiting from a three-dimensionally dense and negatively charged DNA shell, BEV-SNA reduce airway adhesion, enabling deep pulmonary delivery and efficient cellular uptake. In IPF models, BEV-SNA demonstrated multiphase therapeutic effects, including protection of alveolar epithelial cells from ROS, anti-inflammatory activity, and late-stage anti-fibrotic action, effectively halting fibrosis progression and achieving a 50% survival rate in mice. This study presents a novel therapeutic platform combining the natural biomimicry of EVs with the functional adaptability of SNAs, proposing an innovative strategy for pulmonary drug delivery and the treatment of respiratory diseases.

医療・健康
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