A Chimeric Conjugate of Antibody and Programmable DNA Nanoassembly Smartly Activates T Cells for Precise Cancer Cell Targeting

Synthetically directing T‐cells against tumors emerges as a promising strategy in immunotherapy, while it remains challenging to smartly engage T cells with tunable immune response. Herein, we report an intelligent molecular platform to engineer T‐cell recognition for selective activation to potentl...

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Veröffentlicht in:Angewandte Chemie International Edition 2022-09, Vol.61 (36), p.e202205902-n/a
Hauptverfasser: Tang, Rui, Fu, Yu‐Hao, Gong, Bo, Fan, Ying‐Ying, Wang, Hong‐Hui, Huang, Yan, Nie, Zhou, Wei, Ping
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Sprache:eng
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Zusammenfassung:Synthetically directing T‐cells against tumors emerges as a promising strategy in immunotherapy, while it remains challenging to smartly engage T cells with tunable immune response. Herein, we report an intelligent molecular platform to engineer T‐cell recognition for selective activation to potently kill cancer cells. To this end, we fabricated a hybrid conjugate that uses a click‐type DNA–protein conjugation to equip the T cell‐engaging antibody with two distinct programmable DNA nanoassemblies. By integrating multiple aptameric antigen‐recognitions within a dynamic DNA circuit, we achieved combinatorial recognition of triple‐antigens on cancer cells for selective T‐cell activation after high‐order logic operation. Moreover, by coupling a DNA nanostructure, we precisely defined the valence of the antigen‐binding aptamers to tune avidity, realizing effective tumor elimination in vitro and in vivo. Together, we present a versatile and programmable strategy for synthetic immunotherapy. A chimeric antibody‐nucleic acid T‐cell engager (CAN‐TE) redirecting T cells to precisely target and potently kill the cancer cells by coupling 1) a dynamic DNA circuit with high‐order logic function for smart cell recognition or 2) a multivalent aptameric DNA nanostructure to control the targeting avidity for tunable immune response is reported.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.202205902