作者更正:OR7A10 GPCR 工程化增强 CAR-NK 疗法对实体瘤的疗效
Author Correction: OR7A10 GPCR engineering boosts CAR-NK therapy against solid tumours.
FRONTIER PAPERS
Author Correction: OR7A10 GPCR engineering boosts CAR-NK therapy against solid tumours.
Depletion of an immature cord blood NK subset reverses trogocytosis-driven CAR NK dysfunction.
这些发现定义了供者亚群驱动的CAR NK功能障碍机制,并提供了一种提高抗肿瘤效力的生产策略。
Advances and prospects in cell therapy for cancer: explorations from T cells to stem cells.
全球癌症负担日益加重,亟需创新的治疗策略。
Advancing CAR-NK cell therapy in solid tumors: Current landscape and future directions.
嵌合抗原受体(CAR)工程化的自然杀伤(NK)细胞已成为一种有前景的现代免疫治疗策略,相较于CAR-T细胞疗法,其具有先天细胞毒性、安全性特征以及可规模化、现货型异体制造的潜力等优势。
Development of CAR NK Cell Lines Selectively Targeting Cancer Cells Expressing Membrane Hsp70.
有效的基于嵌合抗原受体 (CAR) 的免疫疗法既依赖于合适的免疫细胞平台,也依赖于肿瘤特异性抗原,以克服实体瘤中的屏障。
OR7A10 Overexpression Boosts CAR-NK Therapy Against Solid Tumors.
In vivo CAR-cell therapy: current challenges and emerging therapeutic advances.
体内嵌合抗原受体(CAR)细胞疗法正在经历从传统的体外制造向原位细胞编辑的变革性转变,旨在通过靶向载体递送直接在患者体内生成功能性CAR工程免疫细胞,从而显著提高治疗的可及性和适用性。
Bioengineered cell therapies for pediatric solid tumors: unmet needs and a measurement-integrated approach.
儿童实体瘤仍然构成重大治疗挑战,其生存获益落后于儿童血液系统恶性肿瘤所取得的进展。
Harnessing the Power of CAR-NK Cells for Solid Tumors: Challenges, Innovations, and Future Frontiers in Immunotherapy.
实体瘤仍是肿瘤治疗领域的艰巨挑战,即使是最先进的免疫疗法也常被其逃逸。
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