中文摘要
嵌合抗原受体(CAR)可使T细胞靶向任何表面抗原。然而,CAR需要优化才能对低密度抗原产生活性。Heitzeneder等人对CAR组分进行了迭代调整,最终设计出靶向脑聚糖(GPC2)的CAR,在神经母细胞瘤模型中显示出强效的临床前活性。
展开英文摘要原文
Chimeric antigen receptors (CARs) allow redirection of T cells against any surface antigen. However, CARs require optimization to achieve activity against low-density antigens. Heitzeneder et al. perform an iterative adjustment of CAR components to reach a design for targeting cerebroglycan (GPC2) that shows potent pre-clinical activity in neuroblastoma models.
论文信息
- 作者
- Hotblack A、Straathof K
- 第一作者单位
- University College London (UCL) Great Ormond Street Institute of Child Health, London, UK; UCL Cancer Institute, London, UK.United Kingdom
- 通讯作者单位
- University College London (UCL) Great Ormond Street Institute of Child Health, London, UK; UCL Cancer Institute, London, UK. Electronic address: k.straathof@ucl.ac.uk.United Kingdom
- 文献类型
- 评论
- 期刊
- Cancer cell2022 Jan 10