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.
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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。
Circumventing Ewing sarcoma tumor microenvironment resistance by IL1RAP CAR-modified TGFβ1-imprinted natural killer cells in combination with IL-15 ag
我们的临床前数据表明,利用靶向肿瘤的TGFβ1印记IL1RAP-CAR-NK细胞,联合IL-15激动剂和抗GD2抗体所进行的组合性先天免疫治疗,是一种有前景的针对转移性/复发性/难治性ES的新型治疗策略。
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。
Exploring CAR cell therapies beyond CAR-T for myeloid malignancies.
嵌合抗原受体(CAR)-T细胞在多种血液系统恶性肿瘤中已展现出显著疗效;
Study of TROP2 CAR Engineered IL15-transduced Cord Blood-derived NK Cells Delivered Intraperitoneally for the Management of Platinum Resistant Ovarian
这是一项 I/II 期注册临床试验,评估 CAR-NK 细胞治疗胰腺癌、卵巢癌的安全性、可行性及初步疗效。当前状态:进行中(不再招募)。计划入组 51 例。试验地点:美国 · 休斯顿(共 1 个中心)。登记号:NCT05922930。
Reprogramming Antitumor Immunity: NK Cell Strategies to Navigate the Immunosuppressive Tumor Microenvironment.
肿瘤免疫逃逸是持久癌症免疫治疗的主要障碍,因为晚期恶性肿瘤会形成一种肿瘤微环境(TME),该微环境优先使T细胞应答耗竭和失能。
CAR-NK Cells in B-cell Lymphoma: A New Frontier toward Accessible and Scalable Cellular Therapy.
在这项II期研究中,TAK-007,一种现成的表达IL-15的同种异体CD19 CAR NK细胞疗法,在经过重度预处理的B细胞淋巴瘤患者中(包括CAR-T治疗后患者)显示出令人鼓舞的缓解率、快速的治疗可及性和优异的安全性,尽管持久性有限。
A Phase 2, Open-Label, Multicenter Study of the Safety and Efficacy of TAK-007 in Adult Patients with Relapsed/Refractory B-cell Non-Hodgkin Lymphoma.
不良事件可控,细胞因子释放综合征限于 1-2 级(11.5%)。
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。
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