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:Glioblastoma vaccines: past, present, and opportunities.
Glioblastoma vaccines: past, present, and opportunities.
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胶质母细胞瘤(GBM)是成人中最致命的中枢神经系统(CNS)肿瘤之一。作为标准治疗(SOC)的补充,多种免疫疗法改善了其他癌症的治疗效果。其中,肿瘤疫苗可作为补充性单一疗法,或与其他免疫疗法(如免疫检查点阻断(ICB)和CAR-T 细胞疗法)联合以增强临床疗效。既往针对GBM治疗性疫苗的研究表明,由于突变负荷较低,GBM中可靶向的新抗原较少,且单肽治疗性疫苗作为单一疗法在肿瘤控制方面疗效有限。结合多种抗原,包括新抗原、肿瘤相关抗原(TAAs)和病原体衍生抗原,并优化疫苗设计或接种策略,可能有助于提高临床疗效。在本综述中,我们讨论了当前的GBM治疗性疫苗平台、已评估及潜在的抗原靶点、当前挑战以及疗效改善的前景机遇。
Glioblastoma (GBM) is one of the most lethal central nervous systems (CNS) tumours in adults. As supplements to standard of care (SOC), various immunotherapies improve the therapeutic effect in other cancers. Among them, tumour vaccines can serve as complementary monotherapy or boost the clinical efficacy with other immunotherapies, such as immune checkpoint blockade (ICB) and chimeric antigen receptor T cells (CAR-T) therapy.
Previous studies in GBM therapeutic vaccines have suggested that few neoantigens could be targeted in GBM due to low mutation burden, and single-peptide therapeutic vaccination had limited efficacy in tumour control as monotherapy.
Combining diverse antigens, including neoantigens, tumour-associated antigens (TAAs), and pathogen-derived antigens, and optimizing vaccine design or vaccination strategy may help with clinical efficacy improvement. In this review, we discussed current GBM therapeutic vaccine platforms, evaluated and potential antigenic targets, current challenges, and perspective opportunities for efficacy improvement.
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