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Enhancing Breast Cancer Immunotherapy by Suppressing Sympathetic Nervous System-Driven T-Cell Exhaustion and Promoting T-Cell Priming and Trafficking.

ACS nano 2026 Vol.20(1) p. 931-948

Gao L, Luo Z, Dong L, Gao C, Zhang X, Yong X, Yang H, Zhou Y, Li Y, Liu T, Liang G, Muddassir M, Zhu Y, Xie J

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Immunotherapy has transformed cancer treatment, yet its efficacy in solid tumors such as breast cancer remains limited by weak T cell priming, impaired trafficking, and functional exhaustion within th

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APA Gao L, Luo Z, et al. (2026). Enhancing Breast Cancer Immunotherapy by Suppressing Sympathetic Nervous System-Driven T-Cell Exhaustion and Promoting T-Cell Priming and Trafficking.. ACS nano, 20(1), 931-948. https://doi.org/10.1021/acsnano.5c16178
MLA Gao L, et al.. "Enhancing Breast Cancer Immunotherapy by Suppressing Sympathetic Nervous System-Driven T-Cell Exhaustion and Promoting T-Cell Priming and Trafficking.." ACS nano, vol. 20, no. 1, 2026, pp. 931-948.
PMID 41434779

Abstract

Immunotherapy has transformed cancer treatment, yet its efficacy in solid tumors such as breast cancer remains limited by weak T cell priming, impaired trafficking, and functional exhaustion within the tumor microenvironment. Sympathetic nervous system (SNS) hyperactivation has recently emerged as a driver of T cell exhaustion, representing a therapeutically actionable target. Here, we develop a multifunctional nanoplatform in which irradiated tumor lysate-pulsed dendritic cell (DC) membranes wrap lipid nanoparticles, enabling the codelivery of the β-adrenergic receptor blocker carvedilol and S1PR1 mRNA. These nanovesicles preferentially accumulate in tumor-draining lymph nodes, where they enhance antigen presentation and T cell priming. S1PR1 expression promotes T cell egress and trafficking, while carvedilol attenuates SNS-mediated exhaustion. In combination with PD-L1 blockade, this approach reinforced effector function in tumors, reduced tumor volume by 76%, extended median survival from 30 to 54 days, and achieved complete regression in 60% of animals. By simultaneously targeting priming, trafficking, activation, and exhaustion, this strategy provides an integrated approach to overcoming resistance in breast cancer.

MeSH Terms

Female; Animals; Sympathetic Nervous System; Breast Neoplasms; Immunotherapy; Mice; T-Lymphocytes; Humans; Nanoparticles; Dendritic Cells; Carvedilol; Cell Line, Tumor; Tumor Microenvironment; Mice, Inbred C57BL; T-Cell Exhaustion

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