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:Comparison of the therapeutic potential of exosomes derived from different cells for the treatment of prostate cancer.
前列腺癌(PCa)是男性癌症死亡的主要原因,凸显了对新疗法的迫切需求。
前列腺癌(PCa)是男性癌症死亡的主要原因,凸显了对新疗法的迫切需求。被称为外泌体(EXOs)的天然纳米囊泡因其优异的生物相容性、极低的免疫原性以及固有的携带生物活性货物的能力,已展现出作为治疗载体的巨大前景。不同细胞类型均可产生这些囊泡,且每一种都赋予其独特的生物学特征和治疗过程。本综述比较了来自三种主要来源的EXOs治疗PCa的治疗潜力。我们批判性地审视了间充质干细胞来源的EXOs(MSC-EXOs)的实用性,其利用固有的肿瘤趋向性作为治疗药物的天然递送载体。我们探讨了免疫细胞来源的EXOs(IC-EXOs)作为细胞毒性剂或无细胞疫苗有效激活抗肿瘤免疫的潜力。我们还讨论了肿瘤来源的EXOs(TEXs)的矛盾角色,尽管其参与癌症发展,却可作为疫苗抗原或液体活检工具。通过整合来自多个平台的证据,我们强调了这些平台的独特优势、缺点及最佳治疗环境。最后,我们讨论了关键的临床转化问题,如生产和标准化,并基于特定治疗目标,为在不断发展的PCa治疗领域中选择最佳EXO来源提供了一个框架。
Prostate cancer (PCa) is a primary cause of male cancer death, underlining the crucial need for new therapies. Natural nanovesicles known as exosomes (EXOs) have shown great promise as therapeutic vectors due to their excellent biocompatibility, minimal immunogenicity, and inherent capacity to carry bioactive cargo. Different cell types may produce these vesicles, and each one imparts unique biological characteristics and therapeutic processes. This review compares the therapeutic potential of EXOs obtained from three primary sources for the treatment of PCa. The usefulness of mesenchymal stem cell-derived EXOs (MSC-EXOs), which leverage their inherent tumor tropism to serve as naturally occurring delivery vehicles for therapeutic agents, is critically examined. We investigate the potential of immune cell-derived EXOs (IC-EXOs) as cytotoxic agents or cell-free vaccines that effectively activate anti-tumor immunity. We also discuss the paradoxical role of tumor-derived EXOs (TEXs), which can serve as vaccine antigens or as tools for liquid biopsy, despite their role in cancer development. We highlight the unique benefits, drawbacks, and best therapeutic settings of these platforms by combining evidence from multiple platforms. Lastly, we address crucial clinical translation issues, such as manufacturing and standardization, and offer a framework for selecting the best EXO source in the evolving field of PCa treatment based on specific therapeutic goals.
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