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Updated: Apr 23, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Anti-PD-1-targeted therapies focusing on lymphatic malignancies: biological rationale, clinical challenges and
Meirav Kedmi1, Abraham Avigdor, Arnon Nagler
1Hematology Division, Chaim Sheba Medical Center, Tel Hashomer, and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Abstract:
Cancer immunotherapy with tumor-directed antibodies has generally been very successful, while T-cell immunotherapy has been less effective. Some lymphoid malignancies can be cured with immunochemotherapy but nevertheless many patients relapse or progress in spite of maximal therapy. Both solid tumors and lymphoid malignancies develop mechanisms in order to escape destruction by the intact immune system. One such mechanism is mediated through immune checkpoints. PD-1 (programmed cell death protein-1, which is expressed on activated T and B cells, natural killer cells and myeloid cells, is one of those checkpoints. This review focuses on the effect of PD-1 activation on lymphoid malignancies and its role as a therapeutic target.
Insights
Cancer immunotherapy faces challenges, particularly with T-cell therapies. This review explores programmed cell death protein-1 (PD-1) as a key immune checkpoint and its therapeutic potential in lymphoid malignancies.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Cancer immunotherapy using antibodies shows success, but T-cell therapies are less effective.
- Many patients with lymphoid malignancies relapse despite intensive treatment.
- Tumors employ immune evasion strategies, including immune checkpoints like PD-1.
Purpose of the Study:
- To review the impact of programmed cell death protein-1 (PD-1) activation on lymphoid malignancies.
- To evaluate PD-1 as a therapeutic target for these cancers.
Main Methods:
- Literature review of studies on PD-1 and lymphoid malignancies.
- Analysis of PD-1 expression and function in cancer immunology.
- Examination of PD-1-targeted therapies in preclinical and clinical settings.
Main Results:
- Programmed cell death protein-1 (PD-1) is expressed on various immune cells, acting as a critical checkpoint.
- PD-1 pathway dysregulation contributes to immune evasion in lymphoid malignancies.
- Targeting PD-1 presents a promising therapeutic avenue for certain blood cancers.
Conclusions:
- Immune checkpoints, particularly PD-1, play a significant role in the progression of lymphoid malignancies.
- Modulating the PD-1 pathway offers a potential strategy to overcome immune resistance and improve treatment outcomes.
- Further research into PD-1's role is crucial for developing effective immunotherapies for lymphoid cancers.
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