Development of a Peptide-Based Photoimmunotherapy Drug Targeting PD-L1
Takuya Otani1, Naoya Kondo1, Ayaka Kanai1
1Near InfraRed Photo-ImmunoTherapy Research Institute, Kansai Medical University, Hirakata 573-1010, Osaka, Japan.
Abstract:
Near-infrared photoimmunotherapy (NIR-PIT) has recently attracted attention as a highly selective cancer treatment, with good treatment outcomes observed from the only antibody-based drug currently available for clinical use. However, since only a single agent is currently used clinically and the development of new antibodies is costly, exploring other therapeutic modalities is important. In this study, we investigated a novel peptide-based PIT drug targeting programmed death-ligand 1 (PD-L1), which is overexpressed in many types of cancer. The WL12 peptide, which is known to bind to PD-L1, was conjugated with the photoabsorber IRDye700DX (IR700), and its usefulness was evaluated in vitro and in vivo. In therapeutic experiments on PD-L1-positive cells, NIR-PIT with WL12-IR700 induced PIT-like morphological changes in cells and reduced cancer cell viability in an NIR light dose- and drug concentration-dependent manner. In vivo experiments showed significant suppression of tumor growth and an extended overall survival rate. These results indicate that the developed peptide-based drug can be used for PD-L1-targeted NIR-PIT.
Insights
A new peptide drug targets PD-L1 for near-infrared photoimmunotherapy (NIR-PIT), showing promise for cancer treatment. This novel approach effectively reduced cancer cell viability and suppressed tumor growth in preclinical studies.
Area of Science:
- Oncology
- Immunotherapy
- Bioconjugation
Background:
- Near-infrared photoimmunotherapy (NIR-PIT) offers selective cancer treatment.
- Current NIR-PIT relies on a single antibody-based drug, necessitating exploration of alternative therapeutic agents.
- Programmed death-ligand 1 (PD-L1) is overexpressed in various cancers, making it a viable therapeutic target.
Purpose of the Study:
- To develop and evaluate a novel peptide-based drug for PD-L1-targeted NIR-PIT.
- To assess the efficacy of the peptide-drug conjugate in vitro and in vivo.
Main Methods:
- Conjugation of the PD-L1-binding peptide WL12 with the photoabsorber IRDye700DX (IR700).
- In vitro evaluation of WL12-IR700 efficacy on PD-L1-positive cancer cells under NIR light irradiation.
- In vivo assessment of tumor growth suppression and survival rates in preclinical cancer models.
Main Results:
- WL12-IR700 induced photoimmunotherapy-like cell death in PD-L1-positive cancer cells.
- Cancer cell viability was reduced in a dose- and concentration-dependent manner.
- Significant tumor growth suppression and extended overall survival were observed in vivo.
Conclusions:
- The developed peptide-based drug, WL12-IR700, is effective for PD-L1-targeted NIR-PIT.
- This peptide-drug conjugate represents a promising alternative therapeutic modality for PD-L1-expressing cancers.
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