4.7 Review

Smart Design of Nanostructures for Boosting Tumor Immunogenicity in Cancer Immunotherapy

Journal

PHARMACEUTICS
Volume 15, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics15051427

Keywords

cancer immunotherapy; smart responsive materials; controlled release; synergistic therapy

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Tumor immunotherapy shows promise in oncology, but faces limitations including low response rates and potential off-target effects. Nanotechnology can enhance tumor immunogenicity and improve the success rate of immunotherapy. This review emphasizes the integration of anticancer drugs with multifunctional nanomedicines to upregulate tumor immunogenicity, triggering immune memory and the activation of tumor-specific T-cells. Challenges and personal perspectives on bioengineered nanomaterials for future cancer immunotherapy are also discussed.
Although tumor immunotherapy has emerged as a promising therapeutic method for oncology, it encounters several limitations, especially concerning low response rates and potential off-targets that elicit side effects. Furthermore, tumor immunogenicity is the critical factor that predicts the success rate of immunotherapy, which can be boosted by the application of nanotechnology. Herein, we introduce the current approach of cancer immunotherapy and its challenges and the general methods to enhance tumor immunogenicity. Importantly, this review highlights the integration of anticancer chemo/immuno-based drugs with multifunctional nanomedicines that possess imaging modality to determine tumor location and can respond to stimuli, such as light, pH, magnetic field, or metabolic changes, to trigger chemotherapy, phototherapy, radiotherapy, or catalytic therapy to upregulate tumor immunogenicity. This promotion rouses immunological memory, such as enhanced immunogenic cell death, promoted maturation of dendritic cells, and activation of tumor-specific T cells against cancer. Finally, we express the related challenges and personal perspectives of bioengineered nanomaterials for future cancer immunotherapy.

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