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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Current research progress on extracellular vesicles derived from mesenchymal stem cells in tuberculosis treatment (Review).
Current research progress on extracellular vesicles derived from mesenchymal stem cells in tuberculosis treatment (Review).
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间充质干细胞来源的细胞外囊泡(MSC EVs)因其独特的生物学功能及治疗潜力而受到研究关注。与其来源的亲本 MSC 相比,MSC EVs 通常不会引起全身性过敏反应、溶血、致热反应、血液学异常改变以及血管和肌肉刺激问题,因而具有治疗潜力。本综述对 MSC EVs 的众多分离方法进行了全面分析,每种方法均基于关键参数进行评估,包括原理、优势、局限性和应用。
值得注意的是,MSC EVs 在结核病(TB)治疗中的治疗潜力已受到强调。MSC EVs 已展现出独特的能力,可调节辅助性 T 细胞(Th)1/Th2/T 调节性细胞平衡、促进 M2 巨噬细胞极化、通过 microRNA 介导机制减轻炎症,并通过抗菌肽反应增强宿主防御。将 MSC EVs 与抗 TB 治疗相结合,可通过降低 TNF 水平和提高 IL 10/TGF 比值来改善肺、肾和膀胱健康。
值得注意的是,来源于不同 MSC 来源(如脐带与骨髓细胞)的 EVs 之间存在功能差异,这凸显了制定针对性优化策略的必要性。在临床试验前进行充分的风险评估十分重要,特别是涉及免疫原性、潜在促炎效应以及促进 TB 潜伏的问题。本综述探讨了 MSC EVs 在 TB 及其他感染性疾病中的潜在临床应用,为其治疗潜力提供了关键见解,旨在指导未来研究。
Mesenchymal stem cell derived extracellular vesicles (MSC EVs) have garnered research attention due to their unique biological functionalities and therapeutic potential. Compared with the parent MSCs from which they originate, MSC EVs are typically free from systemic allergic reactions, hemolysis, pyrogenic reactions, abnormal hematological changes, and vascular and muscle irritation problems, and thus, exhibit therapeutic potential.
The present review provides a comprehensive analysis of numerous isolation methodologies for MSC EVs, with each method being evaluated based on key parameters, including principles, advantages, limitations and applications.
Notably, the therapeutic potential of MSC EVs in the treatment of tuberculosis (TB) has been emphasized. MSC EVs have demonstrated unique capacities to modulate the T helper cell (Th)1/Th2/T regulatory cell balance, promote M2 macrophage polarization, alleviate inflammation through microRNA mediated mechanisms and enhance host defense through antimicrobial peptide responses. The integration of MSC EVs with anti TB therapy can improve lung, kidney and bladder health by reducing TNF levels and increasing IL 10/TGF ratios.
Notably, functional discrepancies between EVs derived from distinct MSC sources, such as umbilical cord vs. bone marrow cells, underscore the need for targeted optimization strategies. Adequate risk assessment is important before clinical trials, particularly concerning immunogenicity, potential pro inflammatory effects and promotion of TB latency. The present review explores the potential clinical applications of MSC EVs in TB and other infectious diseases, offering key insights into their therapeutic potential, with the aim of guiding future research.
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