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https://hdl.handle.net/10356/160729
Title: | Activatable polymer nanoenzymes for photodynamic immunometabolic cancer therapy | Authors: | Zeng, Ziling Zhang, Chi Li, Jingchao Cui, Dong Jiang, Yuyan Pu, Kanyi |
Keywords: | Engineering::Bioengineering | Issue Date: | 2021 | Source: | Zeng, Z., Zhang, C., Li, J., Cui, D., Jiang, Y. & Pu, K. (2021). Activatable polymer nanoenzymes for photodynamic immunometabolic cancer therapy. Advanced Materials, 33(4), 2007247-. https://dx.doi.org/10.1002/adma.202007247 | Project: | M4081627.120 2019-T1-002-045 2018-T1-001-173 MOE2018-T2-2-042 |
Journal: | Advanced Materials | Abstract: | Tumor immunometabolism contributes substantially to tumor proliferation and immune cell activity, and thus plays a crucial role in the efficacy of cancer immunotherapy. Modulation of immunometabolism to boost cancer immunotherapy is mostly based on small-molecule inhibitors, which often encounter the issues of off-target adverse effects, drug resistance, and unsustainable response. In contrast, enzymatic therapeutics can potentially bypass these limitations but has been less exploited. Herein, an organic polymer nanoenzyme (SPNK) with near-infrared (NIR) photoactivatable immunotherapeutic effects is reported for photodynamic immunometabolic therapy. SPNK is composed of a semiconducting polymer core conjugated with kynureninase (KYNase) via PEGylated singlet oxygen (1 O2 ) cleavable linker. Upon NIR photoirradiation, SPNK generates 1 O2 not only to exert photodynamic effect to induce the immunogenic cell death of cancer, but also to unleash KYNase and trigger its activity to degrade the immunosuppressive kynurenine (Kyn). Such a combinational effect mediated by SPNK promotes the proliferation and infiltration of effector T cells, enhances systemic antitumor T cell immunity, and ultimately permits inhibition of both primary and distant tumors in living mice. Therefore, this study provides a promising photodynamic approach toward remotely controlled enzymatic immunomodulation for improved anticancer therapy. | URI: | https://hdl.handle.net/10356/160729 | ISSN: | 0935-9648 | DOI: | 10.1002/adma.202007247 | Schools: | School of Chemical and Biomedical Engineering | Rights: | © 2020 Wiley-VCH GmbH. All rights reserved. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SCBE Journal Articles |
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