Engineered Cells as a Test Platform for Radiohaptens in Pretargeted Imaging and Radioimmunotherapy Applications.

TitleEngineered Cells as a Test Platform for Radiohaptens in Pretargeted Imaging and Radioimmunotherapy Applications.
Publication TypeJournal Article
Year of Publication2021
AuthorsDacek 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
JournalBioconjug Chem
Volume32
Issue4
Pagination649-654
Date Published2021 04 21
ISSN1520-4812
KeywordsAnimals, 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.

DOI10.1021/acs.bioconjchem.0c00595
Alternate JournalBioconjug Chem
PubMed ID33819023
PubMed Central IDPMC8284561
Grant ListR01 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)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065