Near-Infrared Fluorescence Imaging of Pancreatic Cancer Using a Fluorescently Labelled Anti-CEA Nanobody Probe: A Preclinical Study.
Labrinus van ManenLizzie D A N de MuynckVictor M BaartShadhvi BhairosinghPieterjan DebieAlexander L VahrmeijerSophie HernotJ Sven D MieogPublished in: Biomolecules (2023)
Molecular fluorescence-guided surgery using near-infrared light has the potential to improve the rate of complete resection of cancer. Typically, monoclonal antibodies are being used as targeting moieties, however smaller fragments, such as single-domain antibodies (i.e., Nanobodies ® ) improve tumor specificity and enable tracer injection on the same day as surgery. In this study, the feasibility of a carcinoembryonic antigen-targeting Nanobody (NbCEA5) conjugated to two zwitterionic dyes (ZW800-1 Forte [ZW800F] and ZW800-1) for visualization of pancreatic ductal adenocarcinoma (PDAC) was investigated. After site-specific conjugation of NbCEA5 to the zwitterionic dyes, binding specificity was evaluated on human PDAC cell lines with flow cytometry. A dose escalation study was performed for both NbCEA5-ZW800F and NbCEA5-ZW800-1 in mice with subcutaneously implanted pancreatic tumors. Fluorescence imaging was performed up to 24 h after intravenous injection. Furthermore, the optimal dose for NbCEA5-ZW800-1 was injected in mice with orthotopically implanted pancreatic tumors. A dose-escalation study showed superior mean fluorescence intensities for NbCEA5-ZW800-1 compared to NbCEA5-ZW800F. In the orthotopic tumor models, NbCEA5-ZW800-1 accumulated specifically in pancreatic tumors with a mean in vivo tumor-to-background ratio of 2.4 (SD = 0.23). This study demonstrated the feasibility and potential advantages of using a CEA-targeted Nanobody conjugated to ZW800-1 for intraoperative PDAC imaging.
Keyphrases
- fluorescence imaging
- photodynamic therapy
- stem cells
- endothelial cells
- bone marrow
- randomized controlled trial
- drug delivery
- squamous cell carcinoma
- high resolution
- clinical trial
- cancer therapy
- flow cytometry
- computed tomography
- high dose
- coronary artery disease
- low dose
- adipose tissue
- mesenchymal stem cells
- percutaneous coronary intervention
- climate change
- patients undergoing
- single molecule
- acute coronary syndrome
- atomic force microscopy