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用于治疗肺炎的表达程序性死亡受体配体1(PD-L1)的细胞外囊泡

PD-L1-Expressing Extracellular Vesicles for the Treatment of Pneumonia.

作者信息

Wu Yi, Wang Heng, Song Anning, Wang Xiaoyu, Ma Qingle, Yao Chenlu, Xu Jialu, Dai Huaxing, Wang Chao, Lu Ting, Xu Fang

机构信息

Institute of Functional Nano & Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, Jiangsu 215123, P. R. China.

Department of Biochemistry and Molecular Biology, Medical College, Soochow University, Suzhou, Jiangsu 215123, China.

出版信息

ACS Biomater Sci Eng. 2023 Nov 13;9(11):6464-6471. doi: 10.1021/acsbiomaterials.3c01173. Epub 2023 Oct 16.

Abstract

Acute respiratory distress syndrome (ARDS) is a severe lung condition with a high mortality rate and a lack of effective drug therapy. In this work, we developed mesenchymal stem cell (MSC)-derived extracellular vesicles with high PD-L1 expression (MSC-EVs-PD-L1) for treating lipopolysaccharide (LPS)-induced pneumonia by intratracheal administration. We found an upregulation of PD-1 expression in the inflammatory region of murine lungs; hence, MSC-EVs-PD-L1 exerted immunosuppressive effects via the PD-1/PD-L1 signaling pathway. Furthermore, we treated LPS-induced pneumonia mice by intratracheal administration, which enabled heavy drug accumulation in the lungs of mice and better therapeutic efficacy compared to systemic administration. Our results suggest that MSC-EVs-PD-L1 has the potential to provide a universal platform technology for the immunotherapy of pneumonia.

摘要

急性呼吸窘迫综合征(ARDS)是一种严重的肺部疾病,死亡率高且缺乏有效的药物治疗方法。在本研究中,我们开发了具有高程序性死亡配体1(PD-L1)表达的间充质干细胞(MSC)来源的细胞外囊泡(MSC-EVs-PD-L1),通过气管内给药治疗脂多糖(LPS)诱导的肺炎。我们发现小鼠肺部炎症区域中程序性死亡受体1(PD-1)表达上调;因此,MSC-EVs-PD-L1通过PD-1/PD-L1信号通路发挥免疫抑制作用。此外,我们通过气管内给药治疗LPS诱导的肺炎小鼠,与全身给药相比,这使得药物在小鼠肺部大量积聚并具有更好的治疗效果。我们的结果表明,MSC-EVs-PD-L1有潜力为肺炎的免疫治疗提供一种通用的平台技术。

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