Evoking robust immunogenic cell death by synergistic sonodynamic therapy and glucose depletion using Au clusters/single atoms modified TiO2 nanosheets

Facilitated by reactive oxygen species (ROS)-involved therapies, tumor cells undergo immunogenic cell death (ICD) to stimulate long-term immunity response. However, it is hard to trigger abundant and large-scale ICD for satisfactory cancer immunotherapy. Herein, a multifunctional sonosensitizer that consists of Au single atoms and clusters anchored on TiO2 nanosheets (named Au-S/C-TiO2) is reported for augmented sonodynamic therapy (SDT) and glucose depletion, which ultimately induce robust ICD due to the improved ROS generation and strong endoplasmic reticulum (ER) stress. The synergy effect between Au cluster/single atom with TiO2 nanosheets intensifies apoptosis and ICD pathways to inhibit 80% of tumor cells through in vivo analyses. Furthermore, immune cells in vivo analyses verify the effectiveness of Au-S/C-TiO2 sonosensitizer towards the induction of antitumor immunity. This study thus reveals that simultaneous presence of ROS generation and strong ER stress can efficiently evoke a strong ICD-mediated immune response.

Automated summary

Facilitated by ROS-involved therapies, tumor cells undergo ICD to stimulate long-term immunity response. However, it is challenging to trigger abundant and large-scale ICD for effective cancer immunotherapy. In this study, a multifunctional sonosensitizer (Au-S/C-TiO2) is developed, which enhances SDT and glucose depletion, leading to robust ICD through increased ROS generation and strong ER stress. The synergy effect between Au cluster/single atom with TiO2 nanosheets intensifies apoptosis and ICD pathways to inhibit 80% of tumor cells. In vivo analyses demonstrate the effectiveness of Au-S/C-TiO2 in inducing antitumor immunity.