Novel FRET-based Immunological Synapse Biosensor for the Prediction of Chimeric Antigen Receptor-T Cell Function

• Published in: Small methods 2024-09, p.e2401016
• Main Authors: Lee, Hae Nim, Lee, Soojin, Hong, Jisu, Yoo, Hyejin, Jeong, Jiyun, Kim, Yong-Woo, Shin, Hyun Mu, Jang, Mihue, Lee, Chang-Han, Kim, Hang-Rae, Seong, Jihye
• Format: Article
• Language: English
• ISSN: 2366-9608; 2366-9608
• DOI: 10.1002/smtd.202401016

Chimeric antigen receptor (CAR)-T cell therapy has revolutionized cancer treatment. CARs are activated at the immunological synapse (IS) when their single-chain variable fragment (scFv) domain engages with an antigen, allowing them to directly eliminate cancer cells. Here, an innovative IS biosensor based on fluorescence resonance energy transfer (FRET) for the real-time assessment of CAR-IS architecture and signaling competence is presented. Using this biosensor, scFv variants for mesothelin-targeting CARs and identified as a novel scFv with enhanced CAR-T cell functionality despite its lower affinity than the original screened. The original CAR promoted internalization and trogocytosis, disrupting stable IS formation and impairing functionality are further observed. These findings emphasize the importance of enhancing IS quality rather than maximizing scFv affinity for superior CAR-T cell responses. Therefore, the FRET-based IS biosensor is a powerful tool for predicting CAR-T cell function, enabling the efficient engineering of next-generation CARs with enhanced antitumor potency.