Wu Yi, Wang Heng, Song Anning, Wang Xiaoyu, Ma Qingle, Yao Chenlu, Xu Jialu, Dai Huaxing, Wang Chao, Lu Ting, Xu Fang
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.
ACS Biomater Sci Eng. 2023 Nov 13;9(11):6464-6471. doi: 10.1021/acsbiomaterials.3c01173. Epub 2023 Oct 16.
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.
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。