间充质干细胞
医学
旁分泌信号
移植
再灌注损伤
炎症
肺移植
微泡
免疫系统
癌症研究
免疫学
药理学
缺血
病理
小RNA
内科学
生物
受体
生物化学
基因
作者
Ichiro Sakanoue,Daisuke Nakajima
标识
DOI:10.1097/mot.0000000000001249
摘要
Purpose of review Ischemia–reperfusion injury (IRI) remains a major challenge in lung transplantation, contributing to early graft dysfunction and negatively affecting long-term outcomes. This review highlights recent advances in the use of mesenchymal stem cells (MSCs) and their extracellular vesicles (EVs) as emerging therapeutic approaches to reduce IRI and improve graft viability. Recent findings MSCs exert beneficial effects through paracrine mechanisms, including the release of EVs that carry bioactive molecules such as microRNAs, cytokines, and growth factors. These vesicles play a critical role in modulating the immune response, reducing inflammation, and promoting tissue repair. In preclinical models, MSCs and EVs have been shown to limit neutrophilic infiltration, downregulate pro-inflammatory mediators, and enhance alveolar fluid clearance. Furthermore, the use of ex vivo lung perfusion (EVLP) has emerged as a promising platform for the controlled administration of MSCs and EVs, allowing for targeted intervention prior to implantation. Summary Accumulating preclinical data support the potential of MSC- and EV-based therapies to mitigate IRI and improve graft function. Clinical translation will depend on refining delivery strategies, determining optimal dosing, and ensuring reproducibility – particularly when integrated with EVLP protocols.
科研通智能强力驱动
Strongly Powered by AbleSci AI