Tc-Labeled Cyclic Peptide Targeting PD-L1 as a Novel Nuclear Imaging Probe

Recent cancer therapies have focused on reducing immune suppression in the tumor microenvironment to prevent cancer progression and metastasis. PD-1 is a checkpoint protein that stops the immune response and is expressed on immune T cells. Cancer cells express a PD-1 ligand (PD-L1) to bind to the T-...

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Veröffentlicht in:Pharmaceutics 2023-11, Vol.15 (12)
Hauptverfasser: Ferro-Flores, Guillermina, Ocampo-García, Blanca, Cruz-Nova, Pedro, Luna-Gutiérrez, Myrna, Bravo-Villegas, Gerardo, Azorín-Vega, Erika, Jiménez-Mancilla, Nallely, Michel-Sánchez, Emiliano, García-Pérez, Osvaldo, Lara-Almazán, Nancy, Santos-Cuevas, Clara
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Sprache:eng
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Zusammenfassung:Recent cancer therapies have focused on reducing immune suppression in the tumor microenvironment to prevent cancer progression and metastasis. PD-1 is a checkpoint protein that stops the immune response and is expressed on immune T cells. Cancer cells express a PD-1 ligand (PD-L1) to bind to the T-cell surface and activate immunosuppressive pathways. This study aimed to design, synthesize, and evaluate a [sup.99m]Tc-labeled PD-L1-targeting cyclic peptide inhibitor ([sup.99m]Tc-iPD-L1) as a novel SPECT radiopharmaceutical for PD-L1 expression imaging. AutoDock software (version 1.5) was used to perform molecular docking for affinity calculations. The chemical synthesis was based on the coupling reaction of 6-hydrazinylpyridine-3-carboxylic acid with a 14-amino-acid cyclic peptide. iPD-L1 was prepared for [sup.99m]Tc labeling. Radio-HPLC was used to verify radiochemical purity. The stability of the radiopeptide in human serum was evaluated by HPLC. iPD-L1 specificity was assessed by SDS-PAGE. [[sup.99m]Tc]Tc-iPD-L1 cellular uptake in PD-L1-positive cancer cells (HCC827 and HCT116) and biodistribution in mice with induced tumors were also performed. One patient with advanced plantar malignant melanoma received [[sup.99m]Tc]Tc-iPD-L1. The iPD-L1 ligand (AutoDock affinity: −6.7 kcal/mol), characterized by UPLC mass, FT-IR, and UV–Vis spectroscopy, was obtained with a chemical purity of 97%. The [[sup.99m]Tc]Tc-iPD-L1 was prepared with a radiochemical purity of >90%. In vitro and in vivo analyses demonstrated [[sup.99m]Tc]Tc-iPD-L1 stability (>90% at 24 h) in human serum, specific recognition for PD-L1, high uptake by the tumor (6.98 ± 0.89% ID/g at 1 h), and rapid hepatobiliary and kidney elimination. [[sup.99m]Tc]Tc-iPD-L1 successfully detected PD-L1-positive lesions in a patient with plantar malignant melanoma. The results obtained in this study warrant further dosimetric and clinical studies to determine the sensitivity and specificity of [[sup.99m]Tc]Tc-iPD-L1/SPECT for PD-L1 expression imaging.
ISSN:1999-4923
1999-4923
DOI:10.3390/pharmaceutics15122662