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用于急性淋巴细胞白血病的靶向CD19的嵌合抗原受体(CAR)T细胞

[Chimeric antigen receptor (CAR) T cells targeting CD19 for acute lymphoblastic leukemia].

作者信息

Takahashi Yoshiyuki, Nishio Nobuhiro

机构信息

Department of Pediatrics, Nagoya University Graduate School of Medicine.

Center for Advanced Medicine and Clinical Research, Department of Advanced Medicine, Nagoya University Hospital.

出版信息

Rinsho Ketsueki. 2023;64(9):1184-1191. doi: 10.11406/rinketsu.64.1184.

Abstract

Chimeric antigen receptor transgenic T cell (CAR-T) therapy targeting the CD19 antigen was approved for relapsed/refractory acute lymphocytic leukemia in the United States in 2017 and in Japan in 2019. Despite the excellent efficacy of CAR-T therapy, the relapse rate is about 50%. To reduce this rate, it will be important to examine predictive factors for relapse and which patients should receive hematopoietic cell transplantation. In addition, as the high cost of CAR-T cells has become a financial toxicity that threatens the health insurance system in many countries, development of less expensive CAR-T products using non-viral vectors is also underway.

摘要

靶向CD19抗原的嵌合抗原受体转基因T细胞(CAR-T)疗法于2017年在美国、2019年在日本被批准用于复发/难治性急性淋巴细胞白血病。尽管CAR-T疗法疗效显著,但复发率约为50%。为降低这一比率,研究复发的预测因素以及哪些患者应接受造血细胞移植将很重要。此外,由于CAR-T细胞的高成本已成为一种财务毒性,威胁到许多国家的医疗保险系统,使用非病毒载体开发成本更低的CAR-T产品的工作也在进行中。

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