Communications Biology (Oct 2024)

DNA origami assembled spheroid for evaluating cytotoxicity and infiltration of chimeric antigen receptor macrophage (CAR-M)

  • Qinyao Zhu,
  • Xiaofang He,
  • Junhua Liu,
  • Heming Wang,
  • Xiaojiao Shan,
  • Guangqi Song,
  • Luo Zhang,
  • Yicheng Zhao,
  • Xiushan Yin

DOI
https://doi.org/10.1038/s42003-024-07009-4
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 9

Abstract

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Abstract Chimeric antigen receptor (CAR) T-cell therapies have shown remarkable results in patients with hematological malignancies. However, their success in treating solid tumors has been limited. As an alternative candidate for the CAR therapy, CAR-macrophages (CAR-M) have demonstrated activation and phagocytosis directed by tumor-associated antigen (TAA), showing promise in the treatment of solid tumors. Nevertheless, the mechanisms by which CARs direct tumor chemotaxis and invasion of CAR-M remain poorly understood. In this study, we aim to investigate the role of CARs in CAR-M attachment and infiltration using 3D tumor spheroids, which were created by utilizing a novel self-assembling nucleic acid nanostructure decorated living cells (NAC). Our results demonstrated that CAR-M exhibited higher invasion and killing capacity in 2D model and 3D tumor spheroids. In summary, the 3D NAC assembled tumor spheroid model provides a suitable platform for target screening and pharmacodynamic evaluation of CAR-M.