| Literature DB >> 33542232 |
Jang Hwan Cho1,2, Atsushi Okuma1,2, Katri Sofjan1,2, Seunghee Lee1,2, James J Collins3,4,5,6,7,8, Wilson W Wong9,10.
Abstract
The immune system is a sophisticated network of different cell types performing complex biocomputation at single-cell and consortium levels. The ability to reprogram such an interconnected multicellular system holds enormous promise in treating various diseases, as exemplified by the use of chimeric antigen receptor (CAR) T cells as cancer therapy. However, most CAR designs lack computation features and cannot reprogram multiple immune cell types in a coordinated manner. Here, leveraging our split, universal, and programmable (SUPRA) CAR system, we develop an inhibitory feature, achieving a three-input logic, and demonstrate that this programmable system is functional in diverse adaptive and innate immune cells. We also create an inducible multi-cellular NIMPLY circuit, kill switch, and a synthetic intercellular communication channel. Our work highlights that a simple split CAR design can generate diverse and complex phenotypes and provide a foundation for engineering an immune cell consortium with user-defined functionalities.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33542232 PMCID: PMC7862674 DOI: 10.1038/s41467-021-21078-7
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919