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Updated: Sep 24, 2025

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Development of cancer immunotherapy based on PD-1/PD-L1 pathway blockade
Min Zhang1, Kehai Liu1, Mingfu Wang1,2
1College of Food Science and Technology, Shanghai Ocean University 999 Hucheng Ring Road Shanghai 201306 China khliu@shou.edu.cn.
Abstract:
Programmed death receptor 1 (PD-1)/programmed death ligand 1 (PD-L1) blockade therapy has achieved considerable success in various tumours. However, only a fraction of patients benefit from its clinical application, and some patients might be suffer from tumour resistance against PD-1/PD-L1 blockade therapy after the original response. In this review, we summarized the main reasons that caused the low response rate of PD-/PD-L1 blockade therapy: firstly, the off-target of PD-1/PD-L1 blocking agents, which is also the main factor of the side effect of autoimmune disorders; secondly, the insufficient infiltration of T cells in a tumour microenvironment; thirdly, the low immunogenicity of tumor cells; fourth, other immunosuppressive components impairing the therapeutic efficacy of the immunotherapy based on the PD-/PD-L1 blockade, and introducing some updated the delivery system of PD-1/PD-L1 blocking agents and the combination therapy based on PD-1/PD-L1 inhibitors and other therapeutics that can complement and promote each other to achieve improved immune response.
Insights
Programmed death receptor 1 (PD-1)/programmed death ligand 1 (PD-L1) blockade therapy shows promise but faces challenges like off-target effects and resistance. Strategies to improve response rates include enhanced T-cell infiltration and combination therapies.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- Programmed death receptor 1 (PD-1)/programmed death ligand 1 (PD-L1) blockade therapy has shown success in treating various cancers.
- However, a significant number of patients do not respond to this therapy, and some develop resistance after initial response.
Purpose of the Study:
- To review the primary reasons for the low response rate and resistance to PD-1/PD-L1 blockade therapy.
- To introduce updated delivery systems and combination therapies to enhance treatment efficacy.
Main Methods:
- Literature review summarizing current understanding of PD-1/PD-L1 blockade limitations.
- Discussion of factors contributing to low response rates and resistance.
- Exploration of novel therapeutic strategies and delivery systems.
Main Results:
- Key factors limiting PD-1/PD-L1 blockade efficacy include off-target effects, insufficient T-cell infiltration, low tumor cell immunogenicity, and other immunosuppressive components.
- Off-target effects are a major cause of autoimmune side effects.
- Updated delivery systems and combination therapies show potential to overcome resistance and improve outcomes.
Conclusions:
- Addressing off-target effects, enhancing T-cell infiltration, and increasing tumor immunogenicity are crucial for improving PD-1/PD-L1 blockade therapy.
- Combination strategies and advanced delivery systems offer promising avenues for enhancing therapeutic efficacy and overcoming resistance in cancer immunotherapy.
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