工程化可控 CAR-T 细胞疗法:从二元安全开关到可编程免疫
Engineering controllable CAR T-cell therapies: from binary safety switches to programmable immunity.
嵌合抗原受体(CAR)T细胞疗法已经彻底改变了癌症基因治疗,但其向实体瘤的拓展受到一个关键弱点的阻碍:传统CAR构建体自主的“始终开启”特性。
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Engineering controllable CAR T-cell therapies: from binary safety switches to programmable immunity.
嵌合抗原受体(CAR)T细胞疗法已经彻底改变了癌症基因治疗,但其向实体瘤的拓展受到一个关键弱点的阻碍:传统CAR构建体自主的“始终开启”特性。
Investigating the role of costimulatory domains in enhancing CAR-T cell persistence in TNBC.
本工作总结了共刺激结构域如何介导CAR-T细胞在三阴性乳腺癌(TNBC)中的持久性、功能和治疗潜力,TNBC是一种高度侵袭性的恶性肿瘤,治疗选择有限且具有免疫抑制性肿瘤微环境。
Defining global priorities in hematopoietic transplantation and cellular therapy: a statement paper from EBMT Global Committee.
大多数受访者(67.1%)报告在JACIE或FACT认证的中心工作。
Combination therapy strategies targeting glypican-3 in hepatocellular carcinoma: A comprehensive review.
肝细胞癌(HCC)仍然是全球癌症相关死亡的主要原因。
Synergistic Oncolytic Effect of HSVtk- and IL-15Rα-Armed Vaccinia Viruses Inducing Systemic Antitumor Immunity.
这些数据表明,在溶瘤痘苗病毒平台中整合直接病毒细胞毒性、HSVtk/GCV介导的自杀基因治疗和IL-15通路靶向免疫调节,可以在严格的乳腺癌模型中提高抗肿瘤疗效。
Reprogramming the tumor microenvironment via TFF3 targeting: a potential novel avenue to boost CAR-T cell therapy in solid tumors.
CAR-T 细胞疗法在血液系统恶性肿瘤中已显示出巨大成功。
Nanotechnology and bioengineering approaches to improve the potency of mesenchymal stem cell as an off-the-shelf versatile tumor delivery vehicle.
靶向癌基因驱动癌症中的可操作突变和免疫肿瘤学的发展是影响癌症治疗范式并导致精准肿瘤学出现的两大显著革命。
Neoantigen T-Cell Receptor Gene Therapy in Pancreatic Cancer.
患者内脏转移灶消退(根据实体瘤疗效评价标准1.1版,总体部分缓解率为72%);缓解在6个月时仍在持续。
Advancements in gene therapy for lung cancer: from genetic insights to clinical applications.
基因治疗是肺癌治疗中一种具有变革性的方法,利用基因替换、编辑和沉默等策略靶向癌基因并恢复抑癌基因功能。
Therapeutic Horizon in Multiple Myeloma: Analysis of the Emerging Landscape of Clinical Trials.
多发性骨髓瘤临床试验的增加凸显了向生物治疗的转变,尤其是免疫治疗和 CAR-T 等基因治疗。
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