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Clickable Universal Tumor-Antigen Equipping Strategy for Remedial Chimeric Antigen Receptor T Cells to Destroy Solid Tumors.

ACS nano 2026

Shabiti S, Pan H, Xu X, Xu S, Xu Z, Zheng J, Zhang X, Li F, Ke Y, Wang Y, Li W, Cai L

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Chimeric antigen receptor (CAR)-T cell therapy has shown striking efficacy in leukemia and lymphoma, but solid tumors remain largely refractory due to the scarcity of tumor-specific antigens and perva

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APA Shabiti S, Pan H, et al. (2026). Clickable Universal Tumor-Antigen Equipping Strategy for Remedial Chimeric Antigen Receptor T Cells to Destroy Solid Tumors.. ACS nano. https://doi.org/10.1021/acsnano.6c00238
MLA Shabiti S, et al.. "Clickable Universal Tumor-Antigen Equipping Strategy for Remedial Chimeric Antigen Receptor T Cells to Destroy Solid Tumors.." ACS nano, 2026.
PMID 42013422

Abstract

Chimeric antigen receptor (CAR)-T cell therapy has shown striking efficacy in leukemia and lymphoma, but solid tumors remain largely refractory due to the scarcity of tumor-specific antigens and pervasive antigen heterogeneity, compounded by rapid CAR-T cell exhaustion that curtails their function and persistence. Here, we propose a clickable universal tumor-antigen equipping (CUTE) strategy in which exogenous antigen is modularly clicked onto the tumor cell surface by metabolic glycoengineering (MGE), remodeling the landscape of tumor antigens. The CUTE strategy yielded a 5.7-fold higher antigen density than endogenous CD19 on Raji cells and markedly increased the functional avidity of CAR-T cells in vitro. The resulting high antigen density stabilized CAR conformations, prevented scFv aggregation-driven tonic signaling, and consequently reduced the exhaustion of CAR-T cells. In both cell-derived and patient-derived xenograft (CDX and PDX) models, the CUTE strategy conferred remedial therapeutic efficacy of CAR-T cells against tumors, significantly prolonging overall survival, with no added toxicity observed. Thus, the CUTE strategy provides a modular platform for redirecting clinically validated CAR-T cells to any solid tumor and offers a potentially translatable route to extend CAR-T therapy beyond hematological cancers.