首页> 外文期刊>Clinical Pharmacology and Therapeutics >Advances in Chimeric Antigen Receptor T-Cell Therapies for Solid Tumors
【24h】

Advances in Chimeric Antigen Receptor T-Cell Therapies for Solid Tumors

机译:嵌合抗原受体T细胞治疗实体肿瘤的研究进展

获取原文
获取原文并翻译 | 示例
           

摘要

In 2017, the US Food and Drug Administration approved the first two novel cellular immunotherapies using synthetic, engineered receptors known as chimeric antigen receptors (CARs), tisagenlecleucel (Kymriah) and axicabtagene ciloleucel (Yescarta), expressed by patient-derived T cells for the treatment of hematological malignancies expressing the B-cell surface antigen CD19 in both pediatric and adult patients. This approval marked a major milestone in the use of antigen-directed "living drugs" for the treatment of relapsed or refractory blood cancers, and with these two approvals, there is increased impetus to expand not only the target antigens but also the tumor types that can be targeted. This state-of-the-art review will focus on the challenges, advances, and novel approaches being used to implement CAR T-cell immunotherapy for the treatment of solid tumors.
机译:2017年,美国食品和药物管理局批准了使用称为嵌合抗原受体(CARS),Tisagenleclecle(Kymriah)和XiscardabTagene Ciloleucel(Yescarta)的合成,工程受体的前两种新细胞免疫疗法,由患者衍生的T细胞表达 治疗在小儿和成年患者中表达B细胞表面抗原CD19的血液学恶性肿瘤。 该批准标志着使用抗原定向的“活药”的主要里程碑,用于治疗复发或难治性血液癌,并且随着这两项认证,不仅增加了靶抗原,而且增加了肿瘤类型的动力增加 可以有针对性的。 这种最先进的综述将侧重于用于实施用于治疗实体肿瘤的汽车T细胞免疫疗法的挑战,进展和新方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号