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10.18632/oncotarget.24179

http://scihub22266oqcxt.onion/10.18632/oncotarget.24179
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C5862632!5862632!29568411
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suck abstract from ncbi


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pmid29568411      Oncotarget 2018 ; 9 (17): 13991-4004
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  • The development of CAR design for tumor CAR-T cell therapy #MMPMID29568411
  • Xu D; Jin G; Chai D; Zhou X; Gu W; Chong Y; Song J; Zheng J
  • Oncotarget 2018[Mar]; 9 (17): 13991-4004 PMID29568411show ga
  • 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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