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In vivo manufacture and manipulation of CAR-T cells for better druggability.
Hou, Rui; Zhang, Xiaoxue; Wang, Xu; Zhao, Xuan; Li, Sijin; Guan, Zhangchun; Cao, Jiang; Liu, Dan; Zheng, Junnian; Shi, Ming.
Afiliação
  • Hou R; College of Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Zhang X; Department of Hematology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Wang X; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Zhao X; Center of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Li S; Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Guan Z; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Cao J; Center of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Liu D; Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Zheng J; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Shi M; Center of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Cancer Metastasis Rev ; 43(3): 1075-1093, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38592427
ABSTRACT
The current CAR-T cell therapy products have been hampered in their druggability due to the personalized preparation required, unclear pharmacokinetic characteristics, and unpredictable adverse reactions. Enabling standardized manufacturing and having clear efficacy and pharmacokinetic characteristics are prerequisites for ensuring the effective practicality of CAR-T cell therapy drugs. This review provides a broad overview of the different approaches for controlling behaviors of CAR-T cells in vivo. The utilization of genetically modified vectors enables in vivo production of CAR-T cells, thereby abbreviating or skipping the lengthy in vitro expansion process. By equipping CAR-T cells with intricately designed control elements, using molecule switches or small-molecule inhibitors, the control of CAR-T cell activity can be achieved. Moreover, the on-off control of CAR-T cell activity would yield potential gains in phenotypic remodeling. These methods provide beneficial references for the future development of safe, controllable, convenient, and suitable for standardized production of CAR-T cell therapy products.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoterapia Adotiva / Receptores de Antígenos Quiméricos / Neoplasias Limite: Animals / Humans Idioma: En Revista: Cancer Metastasis Rev Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoterapia Adotiva / Receptores de Antígenos Quiméricos / Neoplasias Limite: Animals / Humans Idioma: En Revista: Cancer Metastasis Rev Assunto da revista: NEOPLASIAS Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China