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Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Recent Advances in Nanoparticles-Based Platforms Targeting the PD-1/PD-L1 Pathway for Cancer Treatment
Xin Yu1, Chao Fang2, Kun Zhang2
1Department of Oncology, Shanghai Pulmonary Hospital & Thoracic Cancer Institute, Tongji University School of Medicine, Shanghai 200433, China.
Abstract:
Immune checkpoint inhibitors (ICIs) targeting the PD-1/PD-L1 axis showed remarkable improvements in overall response and patient survival, which changed the treatment landscape for multiple cancer types. However, the majority of patients receiving ICIs are either non-responders or eventually develop secondary resistance. Meanwhile, immunological homeostasis would be destroyed as T cell functions are activated excessively, leading to immune-related adverse events (irAEs). Clinically, a large number of irAEs caused by ICIs occurred and affected almost every organ system, resulting in the discontinuation or even the termination of the ongoing therapy. Therefore, researchers are exploring methods to overcome the situations of insufficient accumulation of these drugs in tumor sites and severe side effects. PD-1/PD-L1-targeted agents encapsulated in nanoparticles have emerged as novel drug delivery systems for improving the delivery efficacy, enhancing immune response and minimizing side effects in cancer treatment. Nanocarriers targeting the PD-1/PD-L1 axis showed enhanced functionalities and improved the technical weaknesses based on their reduced off-target effects, biocompatible properties, multifunctional potential and biomimetic modifications. Here, we summarize nanoparticles which are designed to directly target the PD-1/PD-L1 axis. We also discuss the combination of anti-PD-1/PD-L1 agents and other therapies using nanomedicine-based treatments and their anticancer effects, safety issues, and future prospects.
Insights
Nanoparticles delivering immune checkpoint inhibitors targeting PD-1/PD-L1 improve cancer treatment efficacy and reduce side effects. This nanomedicine approach enhances drug delivery and immune response for better patient outcomes.
Area of Science:
- Oncology
- Immunology
- Nanomedicine
Background:
- Immune checkpoint inhibitors (ICIs) targeting the PD-1/PD-L1 axis have transformed cancer therapy, improving survival rates.
- However, many patients do not respond to ICIs or develop resistance, and severe immune-related adverse events (irAEs) limit their use.
- Challenges include poor drug accumulation at tumor sites and significant off-target toxicities.
Purpose of the Study:
- To review nanoparticles designed for direct targeting of the PD-1/PD-L1 axis in cancer treatment.
- To explore nanomedicine strategies combining anti-PD-1/PD-L1 agents with other therapies.
- To discuss the anticancer effects, safety profiles, and future potential of these nanomedicine-based treatments.
Main Methods:
- Summarizing research on nanoparticles engineered to target PD-1/PD-L1 interactions.
- Analyzing nanocarrier properties such as reduced off-target effects, biocompatibility, multifunctionality, and biomimetic modifications.
- Reviewing studies on combination therapies utilizing nanomedicine for enhanced cancer treatment.
Main Results:
- Nanoparticles improve the delivery efficacy of PD-1/PD-L1 inhibitors to tumor sites.
- Nanocarriers enhance anti-tumor immune responses and minimize severe side effects associated with ICIs.
- Targeted nanomedicine approaches show promise in overcoming resistance and improving safety.
Conclusions:
- Nanoparticle-based delivery systems offer a promising strategy to enhance the therapeutic index of PD-1/PD-L1 inhibitors.
- These nanocarriers can overcome limitations of conventional ICIs, improving efficacy and patient safety.
- Future research should focus on optimizing nanomedicine designs and combination strategies for broader clinical application.
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