靶向 B7-H3-CAR-T 细胞中的 Regnase-1 重编程肿瘤微环境并增强骨肉瘤抗肿瘤疗效
Targeting Regnase-1 in B7-H3-CAR T cells reprograms the tumor microenvironment and enhances antitumor efficacy for osteosarcoma.
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Targeting Regnase-1 in B7-H3-CAR T cells reprograms the tumor microenvironment and enhances antitumor efficacy for osteosarcoma.
A conceptual blueprint for "turning cold to hot" in Osteosarcoma: from TME stratification hypotheses to adaptive therapeutic prospects.
Gene-based immunotherapy in osteosarcoma: from oncolytic vectors to engineered immune cells.
Reprogramming adoptive cell therapy for osteosarcoma: engineering, vaccination, and tumor microenvironment remodeling.
RAE1-armoured DC vaccine boosts NKG2D-CAR-T cells elicited anti-solid tumour treatment.
NKG2D.Zeta-NK Cell Conditioning With C7R.GD2.CAR-T Cells for Patients With Relapsed or Refractory Osteosarcoma or Neuroblastoma
这是一项 I 期注册临床试验,评估 GD2NK 细胞治疗神经母细胞瘤、骨肉瘤的疗效与安全性。当前状态:招募中。计划入组 27 例。试验地点:美国 · 休斯顿(共 1 个中心)。登记号:NCT07211737。
The evolution of cellular therapies in sarcoma: Breakthroughs, challenges, and future directions.
Immunotherapy in pediatric bone sarcomas: Current progress and future directions.
CAR-CIK vs. CAR-T: benchmarking novel cytokine-induced killer cells as solid tumor immunotherapy in ErbB2+ rhabdomyosarcoma.
我们的结果表明,CAR-CIK 细胞至少与 CAR-T 细胞效力相当。结合其良好的安全性特征和异体应用可行性,这些发现使 CAR-CIK 细胞成为实体瘤有前景的免疫效应细胞。
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