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The development of CAR design for tumor CAR-T cell therapy.
Xu, Dandan; Jin, Guoliang; Chai, Dafei; Zhou, Xiaowan; Gu, Weiyu; Chong, Yanyun; Song, Jingyuan; Zheng, Junnian.
Afiliação
  • Xu D; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Jin G; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Chai D; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Zhou X; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Gu W; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Chong Y; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Song J; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • Zheng J; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Oncotarget ; 9(17): 13991-14004, 2018 Mar 02.
Article em En | MEDLINE | ID: mdl-29568411
ABSTRACT
In recent years, the chimeric antigen receptor modified T cells (Chimeric antigen receptor T cells, CAR-T) immunotherapy has developed rapidly, which has been considered the most promising therapy. Efforts to enhance the efficacy of CAR-based anti-tumor therapy have been made, such as the improvement of structures of CAR-T cells, including the development of extracellular antigen recognition receptors, intracellular co-stimulatory molecules and the combination application of CARs and synthetic small molecules. In addition, effects on the function of the CAR-T cells that the space distance between the antigen binding domains and tumor targets and the length of the spacer domains have are also being investigated. Given the fast-moving nature of this field, it is necessary to make a summary of the development of CAR-T cells. In this review, we mainly focus on the present design strategies of CAR-T cells with the hope that they can provide insights to increase the anti-tumor efficacy and safety.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article