CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
我们的工作确立了CD81作为连接放射抵抗与免疫逃逸的关键桥梁,其通过维持GBM中CD274的丰度发挥作用,并突显CD81作为优化放射免疫治疗的有前景的治疗靶点。
英文原题:Application of Mesenchymal Stem Cells in Targeted Delivery to the Brain: Potential and Challenges of the Extracellular Vesicle-Based Approach for Brain Tumor Treatment.
治疗脑肿瘤面临巨大挑战,且成人和儿童的预后仍然较差。
治疗脑肿瘤面临巨大挑战,成人和儿童的预后仍然很差。血脑屏障的功能阻碍了新靶点和潜在药物的应用,显著限制了治疗药物进入肿瘤。间充质干细胞(MSCs)能够穿越生物屏障,迁移至损伤部位发挥多种修复效应,并可通过工程化改造装载不同类型的货物,使其成为向中枢神经系统递送抗肿瘤药物的理想载体。MSCs 产生的细胞外囊泡(EVs)(MSC-EVs)具有来自亲本细胞的宝贵固有特性,正被开发为多种神经系统疾病的无细胞疗法。与使用 MSCs 相比,通过 MSC-EVs 进行靶向递送具有更好的药代动力学特征,同时避免了细胞基系统的许多关键问题。随着 MSC 治疗应用领域的迅速扩展,本文旨在为基于 EV 靶向脑肿瘤这一方向提供整体概览,并更新现有技术、实验模型的结果以及这一概念面临的关键挑战。
Treating brain tumors presents enormous challenges, and there are still poor prognoses in both adults and children. Application of novel targets and potential drugs is hindered by the function of the blood-brain barrier, which significantly restricts therapeutic access to the tumor. Mesenchymal stem cells (MSCs) can cross biological barriers, migrate to sites of injuries to exert many healing effects, and be engineered to incorporate different types of cargo, making them an ideal vehicle to transport anti-tumor agents to the central nervous system. Extracellular vesicles (EVs) produced by MSCs (MSC-EVs) have valuable innate properties from parent cells, and are being exploited as cell-free treatments for many neurological diseases. Compared to using MSCs, targeted delivery via MSC-EVs has a better pharmacokinetic profile, yet avoids many critical issues of cell-based systems. As the field of MSC therapeutic applications is quickly expanding, this article aims to give an overall picture for one direction of EV-based targeting of brain tumors, with updates on available techniques, outcomes of experimental models, and critical challenges of this concept.
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