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:Exploring the Tumor-Associated Risk of Mesenchymal Stem Cell Therapy in Veterinary Medicine.
由于与胚胎干细胞和诱导多能干细胞相比,MSC 的肿瘤相关风险更低,MSC 被认为是治疗多种犬类和猫类疾病的合适来源。
间充质干细胞(MSC)疗法已广泛应用于兽医再生医学,用于治疗多种犬猫疾病。随着人们日益重视细胞疗法安全性,对其致瘤潜力的评估需求大幅增加。然而,目前难以直接确认肿瘤究竟源于干细胞还是宿主细胞。此外,既往将高剂量MSC注射到裸鼠体内的研究未发现肿瘤形成。近期研究聚焦于优化兽医患者MSC疗法,例如使用MSC来源细胞外囊泡治疗不同疾病。这一进展也反映出兽医医学向个体化发展的更广泛趋势,即根据宠物独特基因谱量身定制治疗。不同MSC治疗研究结果凸显了其未来在兽医临床应用中的潜力。总之,与胚胎干细胞和诱导多能干细胞相比,MSC相关致瘤风险较低,因此被认为是治疗多种犬猫疾病的合适来源。
Mesenchymal stem cell (MSC) therapy has been actively applied in veterinary regenerative medicine to treat various canine and feline diseases. With increasing emphasis on safe cell-based therapies, evaluations of their tumorigenic potential are in great demand. However, a direct confirmation of whether tumors originate from stem cells or host cells is not easily achievable. Additionally, previous studies evaluating injections of high doses of MSCs into nude mice did not demonstrate tumor formation. Recent research focused on optimizing MSC-based therapies for veterinary patients, such as MSC-derived extracellular vesicles in treating different diseases. This progress also signifies a broader shift towards personalized veterinary medicine, where treatments can be tailored to individual pets based on their unique genetic profiles. These findings related to different treatments using MSCs emphasize their future potential for veterinary clinical applications. In summary, because of lower tumor-associated risk of MSCs as compared to embryonic and induced pluripotent stem cells, MSCs are considered a suitable source for treating various canine and feline diseases.
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