PROTAC 工程化蛋白/DNA 纳米抗原是癌症免疫治疗中树突状细胞疫苗的有效增强剂
PROTAC-Engineered Protein/DNA Nanoantigen is a Potent Booster for Dendritic Cell Vaccines in Cancer Immunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Harnessing Cellular Immunotherapy for EBV-Associated Malignancies: Current Advances and Future Directions.
Harnessing Cellular Immunotherapy for EBV-Associated Malignancies: Current Advances and Future Directions.
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EBV相关恶性肿瘤的标准治疗,如化疗和放疗,在复发/难治性病例中疗效有限,凸显了对创新治疗策略的迫切需求。免疫治疗的最新进展——尤其是EBV特异性细胞毒性T淋巴细胞和树突状细胞疫苗——在治疗和预防方面均显示出前景。工程化T细胞疗法,包括靶向EBV抗原如LMP1和gp350的T细胞受体(TCR)和嵌合抗原受体(CAR)方法,正在临床开发中推进。与传统强化治疗相比,后者通常需要长期给药且伴有显著毒性,细胞免疫治疗具有有利的安全性特征,同时伴随强劲的体内T细胞扩增和强效抗肿瘤作用。尽管临床前和临床试验结果令人鼓舞,但进一步优化治疗方案对于提高疗效和改善不同患者群体的可及性至关重要。在本综述中,我们总结了EBV导向细胞疗法的理论基础,概述了其迄今为止的临床应用,并讨论了当前局限性以及优化这些策略的新兴机遇。
Standard treatments for EBV-associated malignancies, such as chemotherapy and radiotherapy, demonstrate limited efficacy in relapsed or refractory cases, underscoring an urgent need for innovative therapeutic strategies. Recent advances in immunotherapy-particularly EBV-specific cytotoxic T lymphocytes and dendritic cell vaccines-have shown promise for both treatment and prevention. Engineered T cell therapies, including T-cell receptor (TCR) and chimeric antigen receptor (CAR) approaches targeting EBV antigens such as LMP1 and gp350, are progressing in clinical development.
Compared to conventional intensive therapies, which often require prolonged administration and are associated with significant toxicity, cellular immunotherapy offers a favourable safety profile alongside robust in vivo T cell expansion and potent antitumor effects.
Although preclinical and clinical trial results are encouraging, further refinement of therapeutic protocols is critical to enhance efficacy and improve access for diverse patient populations. In this review, we summarise the rationale for EBV-directed cellular therapies, outline their clinical applications to date, and discuss current limitations as well as emerging opportunities to optimise these strategies.
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