细胞
嵌合抗原受体
外周血单个核细胞
细胞生物学
化学
癌细胞
受体
配体(生物化学)
生物物理学
生物
T细胞
生物化学
癌症
体外
免疫学
免疫系统
遗传学
作者
Kari Gabrielse,Amit Gangar,Nigam Kumar,Jae Chul Lee,Adrian Fegan,Jing Shen,Qing Li,Daniel A. Vallera,Carston R. Wagner
标识
DOI:10.1002/anie.201310645
摘要
Abstract The ability to engineer and re‐program the surfaces of cells would provide an enabling synthetic biological method for the design of cell‐ and tissue‐based therapies. A new cell surface‐engineering strategy is described that uses lipid‐chemically self‐assembled nanorings (lipid‐CSANs) that can be used for the stable and reversible modification of any cell surface with a molecular reporter or targeting ligand. In the presence of a non‐toxic FDA‐approved drug, the nanorings were quickly disassembled and the cell–cell interactions reversed. Similar to T‐cells genetically engineered to express chimeric antigen receptors (CARS), when activated peripheral blood mononuclear cells (PBMCs) were functionalized with the anti‐EpCAM‐lipid‐CSANs, they were shown to selectively kill antigen‐positive cancer cells. Taken together, these results demonstrate that lipid‐CSANs have the potential to be a rapid, stable, and general method for the reversible engineering of cell surfaces and cell–cell interactions.
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