Nano-Biohybrid DNA Engager That Reprograms the T-Cell Receptor.
Pei-Qiang MaTian-Xian LiuHua-Dong LiBin-Cheng YinBang-Ce YePublished in: Journal of the American Chemical Society (2022)
Although engineered T cells with transgenic chimeric antigen receptors (CARs) have made a breakthrough in cancer therapeutics, this approach still faces many challenges in the specificity, efficacy, and self-safety of genetic engineering. Here, we developed a nano-biohybrid DNA engager-reprogrammed T-cell receptor (EN-TCR) system to improve the specificity and efficacy, mitigate the excessive activation, and shield against risks from transgenesis, thus achieving a diversiform and precise control of the T-cell response. Utilizing modular assembly, the EN-TCR system can graft different specificities on T cells via antibody assembly. Besides, the designability of DNA hybridization enables precise target recognition by the library of multiantigen cell recognition circuits and allows gradual tuning of the T-cell activation level by the signaling switch and independent control over different types of T cells. Furthermore, we demonstrated the effectiveness of the system in tumor models. Together, this study provides a nongenetic T-cell engineering strategy to overcome major hindrances in T-cell therapy and may be extended to a general and convenient cell engineering strategy.
Keyphrases
- cell therapy
- circulating tumor
- single molecule
- stem cells
- cell free
- mesenchymal stem cells
- nucleic acid
- regulatory t cells
- single cell
- randomized controlled trial
- systematic review
- small molecule
- papillary thyroid
- squamous cell carcinoma
- young adults
- immune response
- weight gain
- bone marrow
- human health
- risk assessment
- dna methylation
- climate change
- structural basis
- lymph node metastasis