An Engineered Bacterium-Based Lactate Bioconsumer for Regulating Immunosuppressive Tumor Microenvironment to Potentiate Antitumor Immunity AITranslate
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In this study, a bacterium-based lactate bioconsumer (designated Bac@RFH) was elaborately engineered for persistent lactate consumption to potentiate antitumor immunotherapy. Specifically, Shewanella oneidensis MR-1 was surface-modified with RFH nanoparticles (R848-loaded Fe-TCPP metal–organic framework nanoparticles coated with hyaluronic acid) via covalent borate ester bonds to prepare Bac@RFH bioconsumer, which could specifically target and colonize in tumors to efficiently metabolize intratumoral lactate and concurrently trigger the reduction of the Fe3+ moieties of RFH through bacteria-mediated electron transfer, resulting in the decomposition of RFH to release Fe2+ and R848. Moreover, the overexpressed H2O2 in the tumor microenvironment (TME) was catalyzed by the Fe2+-driven Fenton reaction to produce cytotoxic ROS, which elicited immunogenic cell death of tumor cells, resulting in DCs maturation and effector T cells activation to eliminate tumors. With the combination of R848-mediated immune activation, Bac@RFH could significantly reshape the immunosuppressive TME for boosting antitumor immunity, such as reducing the recruitment of Tregs and MDSCs as well as promoting the M2-to-M1 polarization of tumor-associated macrophages. In addition, the synergy of Bac@RFH and αPD-1 could evoke robust immune responses to suppress tumor growth and achieve a tumor suppression rate over 90%, which represents a smart strategy to potentiate antitumor immunotherapy via bacterium-based metabolic regulation.
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DOI:https://doi.org/10.1021/acsmaterialslett.3c00749
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In this study, a bacterium-based lactate bioconsumer (designated Bac@RFH) was elaborately engineered for persistent lactate consumption to potentiate antitumor immunotherapy. Specifically, Shewanella oneidensis MR-1 was surface-modified with RFH nanoparticles (R848-loaded Fe-TCPP metal–organic framework nanoparticles coated with hyaluronic acid) via covalent borate ester bonds to prepare Bac@RFH bioconsumer, which could specifically target and colonize in tumors to efficiently metabolize intratumoral lactate and concurrently trigger the reduction of the Fe3+ moieties of RFH through bacteria-mediated electron transfer, resulting in the decomposition of RFH to release Fe2+ and R848. Moreover, the overexpressed H2O2 in the tumor microenvironment (TME) was catalyzed by the Fe2+-driven Fenton reaction to produce cytotoxic ROS, which elicited immunogenic cell death of tumor cells, resulting in DCs maturation and effector T cells activation to eliminate tumors. With the combination of R848-mediated immune activation, Bac@RFH could significantly reshape the immunosuppressive TME for boosting antitumor immunity, such as reducing the recruitment of Tregs and MDSCs as well as promoting the M2-to-M1 polarization of tumor-associated macrophages. In addition, the synergy of Bac@RFH and αPD-1 could evoke robust immune responses to suppress tumor growth and achieve a tumor suppression rate over 90%, which represents a smart strategy to potentiate antitumor immunotherapy via bacterium-based metabolic regulation.
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| GB/T 7714-2015 | [1] ShiMan Zhang, XiaoKang Jin, GuoFeng Luo, et al. ACS Materials Letters, 2023(5). DOI:10.1021/acsmaterialslett.3c00749. |
| MLA | [1] ShiMan Zhang, et al., ACS Materials Letters, no. 5, 2023, https://doi.org/10.1021/acsmaterialslett.3c00749. |
| APA | [1] ShiMan Zhang, XiaoKang Jin, GuoFeng Luo, JunLong Liang, YuZhang Wang, JiaWei Wang, Ran Meng, YanTong Lin, WeiHai Chen, & XianZheng Zhang. (2023). ACS Materials Letters(5). https://doi.org/10.1021/acsmaterialslett.3c00749 |
| IEEE | [1] ShiMan Zhang, XiaoKang Jin, GuoFeng Luo, JunLong Liang, YuZhang Wang, JiaWei Wang, Ran Meng, YanTong Lin, WeiHai Chen, and XianZheng Zhang, ACS Materials Letters, no. 5, 2023, doi: 10.1021/acsmaterialslett.3c00749. |
