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嵌合抗原受体 T 细胞疗法治疗急性淋巴细胞白血病。

Chimeric Antigen Receptor T Cell Therapy for Acute Lymphoblastic Leukemia.

机构信息

Division of Hematology and Oncology, Medical College of Wisconsin, 9200 W. Wisconsin Ave, Milwaukee, WI, 53226, USA.

出版信息

Curr Treat Options Oncol. 2020 Feb 5;21(2):16. doi: 10.1007/s11864-020-0706-6.

DOI:10.1007/s11864-020-0706-6
PMID:32025828
Abstract

Chimeric receptor antigen (CAR) T cells are an innovative cellular immunotherapeutic approach that involves genetic modification of T cells to express CAR targeting tumor antigen. Prior to the development of CAR-T, the only potential cure for patients with relapsed or refractory (RR) acute lymphoblastic leukemia (ALL) was allogeneic hematopoietic stem cell transplantation (HSCT). Several CAR-T cell products have been studied in prospective clinical trials which ultimately have resulted in the approval of one anti-CD19 CAR-T cell product in pediatric RR ALL: tisagenlecleucel (CD3ζ and 41BB). While some patients achieve durable responses with CAR-T, lack of response and relapse remains clinical challenges. Reasons for sub-optimal response include lack of CAR-T cell persistence and target antigen down-regulation. Future CARs are under development to improve long-term persistence and to be able to overcome resistance mechanisms associated with the disease and the hostile tumor microenvironment. With evolving understanding about CARs and new constructs under investigation, there is optimism that future products will improve the safety and efficacy from the current standard of care.

摘要

嵌合抗原受体 (CAR) T 细胞是一种创新的细胞免疫治疗方法,涉及对 T 细胞进行基因修饰以表达靶向肿瘤抗原的 CAR。在 CAR-T 开发之前,复发或难治性 (RR) 急性淋巴细胞白血病 (ALL) 患者唯一潜在的治愈方法是异体造血干细胞移植 (HSCT)。已经在前瞻性临床试验中研究了几种 CAR-T 细胞产品,最终导致一种抗 CD19 CAR-T 细胞产品在儿科 RR ALL 中的批准:tisagenlecleucel(CD3ζ 和 41BB)。虽然一些患者通过 CAR-T 获得了持久的反应,但缺乏反应和复发仍然是临床挑战。反应不佳的原因包括 CAR-T 细胞持久性差和靶抗原下调。正在开发未来的 CAR 以提高长期持久性,并能够克服与疾病和恶劣肿瘤微环境相关的耐药机制。随着对 CAR 和正在研究的新结构的理解不断发展,人们乐观地认为未来的产品将提高现有治疗标准的安全性和疗效。

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Chimeric Antigen Receptor Therapy.嵌合抗原受体疗法
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Improved CNS exposure to tocilizumab after cerebrospinal fluid compared to intravenous administration in rhesus macaques.与静脉注射相比,恒河猴脑脊液注射托珠单抗后中枢神经系统暴露情况有所改善。
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