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Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

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Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
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Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
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Nanotechnology-based PD-L1 siRNA codelivery systems for improving cancer immunotherapy.

Naghmeh Jabarimani1, Mohammad Saleh Sadeghi1, Maryam Edalat2

  • 1Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

Journal of Drug Targeting
|December 17, 2025
PubMed
Summary

Small interfering RNA (siRNA) nanoparticles offer targeted cancer immunotherapy by silencing Programmed death-ligand 1 (PD-L1). This approach enhances combination therapies, improving treatment efficacy and reducing side effects compared to antibody-based methods.

Keywords:
PD-L1 siRNAcodeliveyimmunotherapylipidic nanoparticlepolymeric nanoparticle

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Area of Science:

  • Oncology
  • Immunology
  • Nanotechnology

Background:

  • Immune checkpoint blockade targeting the PD-1/PD-L1 axis revolutionized cancer therapy but faces limitations like off-target effects and limited efficacy in monotherapy.
  • Antibodies lack specificity and only target cell-surface proteins, while intracellular PD-L1 can evade immune surveillance.

Purpose of the Study:

  • To review nanoparticle-based strategies for codelivering PD-L1 siRNA with other therapeutic agents for enhanced cancer immunotherapy.
  • To discuss the mechanisms of PD-L1-mediated tumor immune evasion and how siRNA can overcome these.

Main Methods:

  • Review of polymer and lipid nanoparticles for codelivery of PD-L1 siRNA and other therapeutics.
  • Analysis of nanoparticle properties for tumor targeting, responsiveness, and versatility in combination therapy.

Main Results:

  • Nanoparticles can overcome RNA delivery challenges, enabling targeted delivery of PD-L1 siRNA.
  • Codelivery systems show promise for combinatorial immunotherapy, potentially improving efficacy and reducing systemic toxicity.

Conclusions:

  • Nanoparticle-based combinatorial immunotherapy, particularly with PD-L1 siRNA, presents a promising strategy to overcome limitations of current treatments.
  • Further research and clinical translation are needed to realize the full potential of these advanced therapeutic platforms.