Title | Engineered Cells as a Test Platform for Radiohaptens in Pretargeted Imaging and Radioimmunotherapy Applications. |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Dacek MM, Veach DR, Cheal SM, Carter LM, McDevitt MR, Punzalan B, Vargas DBurnes, Kubik TZ, Monette S, Santich BH, Yang G, Ouerfelli O, Kesner AL, Cheung N-KV, Scheinberg DA, Larson SM, Krebs S |
Journal | Bioconjug Chem |
Volume | 32 |
Issue | 4 |
Pagination | 649-654 |
Date Published | 2021 04 21 |
ISSN | 1520-4812 |
Keywords | Animals, Autoradiography, Cell Engineering, Haptens, HEK293 Cells, Humans, Mice, Positron Emission Tomography Computed Tomography, Radioimmunotherapy, Radiopharmaceuticals, Tissue Distribution, Xenograft Model Antitumor Assays |
Abstract | Pretargeted imaging and radioimmunotherapy approaches are designed to have superior targeting properties over directly targeted antibodies but impose more complex pharmacology, which hinders efforts to optimize the ligands prior to human applications. Human embryonic kidney 293T cells expressing the humanized single-chain variable fragment (scFv) C825 (huC825) with high-affinity for DOTA-haptens (293T-huC825) in a transmembrane-anchored format eliminated the requirement to use other pretargeting reagents and provided a simplified, accelerated assay of radiohapten capture while offering normalized cell surface expression of the molecular target of interest. Using binding assays, biodistribution, and imaging, we demonstrated that radiohaptens based on benzyl-DOTA and a second generation "Proteus" DOTA-platform effectively and specifically engaged membrane-bound huC825, achieving favorable tumor-to-normal tissue uptake ratios in mice. Furthermore, [Y]Y-DOTA-Bn predicted absorbed dose to critical organs with reasonable accuracy for both [Lu]Lu-DOTA-Bn and [Ac]Ac-Pr, which highlights the benefit of a dosimetry-based treatment approach. |
DOI | 10.1021/acs.bioconjchem.0c00595 |
Alternate Journal | Bioconjug Chem |
PubMed ID | 33819023 |
PubMed Central ID | PMC8284561 |
Grant List | R01 CA055349 / CA / NCI NIH HHS / United States P01 CA023766 / CA / NCI NIH HHS / United States F32 EB025050 / EB / NIBIB NIH HHS / United States P50 CA192937 / CA / NCI NIH HHS / United States P30 CA008748 / CA / NCI NIH HHS / United States F31 CA239511 / CA / NCI NIH HHS / United States UL1 TR002384 / TR / NCATS NIH HHS / United States K12 CA184746 / CA / NCI NIH HHS / United States R01 CA233896 / CA / NCI NIH HHS / United States R50 CA243895 / CA / NCI NIH HHS / United States |
Related Institute:
Molecular Imaging Innovations Institute (MI3)