Abstract | Background:
Prostate cancer (PCa) poses a significant global health threaten. Immunotherapy has emerged as a novel strategy to augment the inhibition of tumor proliferation. However, the sole use of anti-PD-L1 Ab for PCa has not yielded improvements, mirroring outcomes observed in other tumor types. Methods: This study employed the thin film hydration method to develop lipid nanobubbles (NBs) encapsulating chlorin e6 (Ce6) and anti-PD-L1 Ab (Ce6@aPD-L1 NBs). Our experimental approach included cellular assays and mouse immunization, providing a comprehensive evaluation of Ce6@aPD-L1 NBs' impact. Results: The Ce6@aPD-L1 NBs effectively induced reactive oxygen species generation, leading to tumor cells death. In mice, they demonstrated a remarkable enhancement of immune responses compared to control groups. These immune responses encompassed immunogenic cell death induced by sonodynamic therapy and PD-1/PD-L1 blockade, activating dendritic cells maturation and effectively stimulating CD8+T cells. Conclusion: Ce6@aPD-L1 NBs facilitate tumor-targeted delivery, activating anti- tumor effects through direct sonodynamic therapy action and immune system reactivation in the tumor microenvironment. Ce6@aPD-L1 NBs exhibit substantial potential for achieving synergistic anti- cancer effects in PCa.
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Authors | Xin Huang, Yueying Chen, Fanglu Zhong, Bin Gui, Yugang Hu, Yuxin Guo, Qing Deng, Qing Zhou |
Journal | International journal of nanomedicine
(Int J Nanomedicine)
Vol. 19
Pg. 2793-2806
( 2024)
ISSN: 1178-2013 [Electronic] New Zealand |
PMID | 38525011
(Publication Type: Journal Article)
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Copyright | © 2024 Huang et al. |
Topics |
- Humans
- Male
- Mice
- Animals
- Ultrasonic Therapy
(methods)
- Ultrasonography
- Prostatic Neoplasms
(drug therapy)
- Photochemotherapy
(methods)
- Immunotherapy
- Cell Line, Tumor
- Tumor Microenvironment
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