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:Clinical progress in the development of CAR T cells to treat malignant glioma.
Clinical progress in the development of CAR T cells to treat malignant glioma.
在研 CAR-T 细胞疗法的快速演进预示着胶质瘤治疗未来的巨大潜力。
背景:嵌合抗原受体(CAR)T细胞疗法是令人振奋的免疫治疗方式,彻底改变了血液系统恶性肿瘤治疗。然而,由于生物学、解剖学和免疫学等多方面因素,将这一成功转化到胶质母细胞瘤(GBM)和弥漫性中线胶质瘤(DMG)等恶性胶质瘤仍面临巨大挑战。尽管如此,过去十年开展的多项临床试验提高了CAR-T治疗胶质瘤的希望。 证据综述:本文重点介绍胶质瘤CAR-T疗法的历史和正在进行的临床试验,聚焦IL-13Rα2、HER2、EGFR、EGFRvIII、EphA2、GD2和B7-H3等关键肿瘤相关抗原。早期研究验证了抗原特异性CAR-T靶向的概念,但抗原下调、CAR-T细胞持久性有限等免疫逃逸机制仍是重大障碍。包括多抗原靶向、替代细胞来源和递送途径创新在内的近期策略,为克服这些挑战提供了有前景的方法。 结论:研究性CAR-T疗法快速发展,预示其未来治疗胶质瘤具有巨大潜力。未来研究需改进抗原靶向策略、优化CAR-T细胞持久性并整合联合方案,充分发挥此疗法的治疗潜力,扩大其治疗脑肿瘤的治疗窗。
CONTEXT: Chimeric antigen receptor (CAR) T cell therapy is an exciting modality of immunotherapy that has revolutionized the treatment of hematologic malignancies. However, translating this success to malignant gliomas such as glioblastoma (GBM) and diffuse midline glioma (DMG) remains a formidable challenge due to multiple biologic, anatomic, and immunologic factors. Despite these hurdles, a number of clinical trials deployed over the last decade have increased optimism for the potential of CAR T cell therapy in glioma treatment. EVIDENCE SYNTHESIS: We highlight historical and ongoing clinical trials of CAR T cell therapy in glioma, with a focus on key tumor-associated antigens such as IL-13R 2, HER2, EGFR, EGFRvIII, EphA2, GD2, and B7-H3. Early studies established proof-of-concept for antigen-specific CAR T cell targeting, yet immune evasion mechanisms such as antigen downregulation and limited CAR T cell persistence remain significant obstacles. Recent approaches, including multiantigen targeting, alternative cell sources, and innovations in delivery routes offer promising strategies to overcome these challenges. CONCLUSIONS: The rapid evolution of investigational CAR T cell therapies portends great potential for the future of glioma treatment. Future studies will need to refine antigen targeting strategies, optimize CAR T cell persistence, and integrate combinatorial approaches to fully harness the therapeutic potential of this modality and improve the therapeutic window against brain tumors.
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