CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Hallmarks of the Tumour Microenvironment of Gliomas and Its Interaction with Emerging Immunotherapy Modalities.
Hallmarks of the Tumour Microenvironment of Gliomas and Its Interaction with Emerging Immunotherapy Modalities.
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胶质瘤是起源于胶质细胞的侵袭性原发性中枢神经系统肿瘤。胶质母细胞瘤是最恶性的类型。它们以预后差或中位总生存期短而闻名。当前的标准治疗被异质性、免疫抑制性肿瘤微环境所压倒,该微环境促进免疫逃逸和肿瘤增殖。免疫治疗及其各种模式——免疫检查点抑制剂、癌症疫苗、溶瘤病毒以及CAR-T 细胞和 NK 细胞——的出现已显示出前景。纳入联合免疫治疗的临床试验已克服微环境耐药性,并产生了有前景的生存和预后获益。以低成本、高通量方式在真实世界场景中推广这些新疗法是当前未满足的需求。这些将对胶质瘤治疗格局产生改变实践的影响。在此,我们综述胶质瘤 TME 的免疫生物学标志、TME 如何逃逸免疫治疗,以及为克服这种相互作用正在进行的工作。
Gliomas are aggressive, primary central nervous system tumours arising from glial cells. Glioblastomas are the most malignant. They are known for their poor prognosis or median overall survival. The current standard of care is overwhelmed by the heterogeneous, immunosuppressive tumour microenvironment promoting immune evasion and tumour proliferation. The advent of immunotherapy with its various modalities-immune checkpoint inhibitors, cancer vaccines, oncolytic viruses and chimeric antigen receptor T cells and NK cells-has shown promise.
Clinical trials incorporating combination immunotherapies have overcome the microenvironment resistance and yielded promising survival and prognostic benefits. Rolling these new therapies out in the real-world scenario in a low-cost, high-throughput manner is the unmet need of the hour. These will have practice-changing implications to the glioma treatment landscape.
Here, we review the immunobiological hallmarks of the TME of gliomas, how the TME evades immunotherapies and the work that is being conducted to overcome this interplay.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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