4.7 Article

Antigen-Capturing Mesoporous Silica Nanoparticles Enhance the Radiation-Induced Abscopal Effect in Murine Hepatocellular Carcinoma Hepa1-6 Models

Journal

PHARMACEUTICS
Volume 13, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics13111811

Keywords

mesoporous silica nanoparticles; radiotherapy; immunotherapy; tumor microenvironment; abscopal effect

Funding

  1. National Research Foundation of Korea (NRF) - Korean government [2017M3A9G5082642, 2018R1A2B2002835, 2019R1A2C1008021]
  2. National Research Foundation of Korea [2018R1A2B2002835, 2019R1A2C1008021, 2017M3A9G5082642] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study investigated the use of mesoporous silica nanoparticles (MSNs) to enhance the effects of radiotherapy (8 Gy of X-rays) on tumors in mice models. Results showed that MSNs enhanced tumor infiltration of cytotoxic T cells and suppressed regulatory T cells, leading to systemic tumor regression. MSNs were found to capture tumor antigens released after RT, which activated dendritic cells and ultimately led to improved anti-tumor effects.
Immunomodulation by radiotherapy (RT) is an emerging strategy for improving cancer immunotherapy. Nanomaterials have been employed as innovative tools for cancer therapy. This study aimed to investigate whether mesoporous silica nanoparticles (MSNs) enhance RT-mediated local tumor control and the abscopal effect by stimulating anti-cancer immunity. Hepa1-6 murine hepatocellular carcinoma syngeneic models and immunophenotyping with flow cytometry were used to evaluate the immune responses. When mice harboring bilateral tumors received 8 Gy of X-rays on a single tumor, the direct injection of MSNs into irradiated tumors enhanced the growth inhibition of irradiated and unirradiated contralateral tumors. MSNs enhanced RT-induced tumor infiltration of cytotoxic T cells on both sides and suppressed RT-enhanced infiltration of regulatory T cells. The administration of MSNs pre-incubated with irradiated cell-conditioned medium enhanced the anti-tumor effect of anti-PD1 compared to the as-synthesized MSNs. Intracellular uptake of MSNs activated JAWS II dendritic cells (DCs), which were consistently observed in DCs in tumor-draining lymph nodes (TDLNs). Our findings suggest that MSNs may capture tumor antigens released after RT, which is followed by DC maturation in TDLNs and infiltration of cytotoxic T cells in tumors, thereby leading to systemic tumor regression. Our results suggest that MSNs can be applied as an adjuvant for in situ cancer vaccines with RT.

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