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Targeted Ultrasound Nanobubbles Therapy for Prostate Cancer via Immuno-Sonodynamic Effect.

AbstractBackground:
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.
AuthorsXin Huang, Yueying Chen, Fanglu Zhong, Bin Gui, Yugang Hu, Yuxin Guo, Qing Deng, Qing Zhou
JournalInternational journal of nanomedicine (Int J Nanomedicine) Vol. 19 Pg. 2793-2806 ( 2024) ISSN: 1178-2013 [Electronic] New Zealand
PMID38525011 (Publication Type: Journal Article)
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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