Biocompatible Glycoconjugation Enables Sensitive In Vivo Cell Tracking by PET/CT

High Resolution Image Download MS PowerPoint Slide Cell-based therapies have transformed the treatment landscape for cancer, yet their clinical translation remains limited by unpredictable in vivo behavior and variable patient responses. Accurate, noninvasive image-based tracking of therapeutic cells, such as PET/CT, is essential for understanding biodistribution, improving safety, and optimizing the design of next-generation treatments. However, existing radiolabeling strategies for cell tracking using PET/CT lack the stability and sensitivity required for reliable long-term imaging. Here, we present a direct radiolabeling strategy that oxidizes cell surface sialic acids to conjugate aminooxy-DFO (AOD) and subsequently radiolabels cells with 89 Zr under biocompatible conditions. We radiolabeled five human and nonhuman primate immune cell types with high radiochemical incorporation (17–194 μCi per million cells) and purity (∼90%), while preserving cell viability. Serial PET/CT imaging over 7–8 days revealed conserved biodistribution patterns across all cell types tested. This approach provides a robust, applicable platform for longitudinal PET/CT tracking of therapeutic cells.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-06-24
DOI
https://doi.org/10.1021/acs.jmedchem.6c00538
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.00

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article

Biocompatible Glycoconjugation Enables Sensitive In Vivo Cell Tracking by PET/CT

Anna S. Thickens, Slukvin, Johnathan J. Caldon, Peiman Hematti et al.
Journal of Medicinal Chemistry
Nanoplatforms for cancer theranostics
article

Biocompatible Glycoconjugation Enables Sensitive In Vivo Cell Tracking by PET/CT

Anna S. Thickens, Slukvin, Johnathan J. Caldon, Peiman Hematti, Christian M. Capitini, Zachary T. Rosenkrans, Victor Santoro-Fernandes, Jason C. Mixdorf, Jonathan W. Engle, Reinier Hernandez, Matthew H. Forsberg, Anatoly N. Pinchuk, Nathan Clemons, Eduardo Aluicio-Sarduy, John Kink, Liudmila Lambert Lepesevich, Saritha S. D’Souza
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Cell-based therapies have transformed the treatment landscape for cancer, yet their clinical translation remains limited by unpredictable in vivo behavior and variable patient responses. Accurate, noninvasive image-based tracking of therapeutic cells, such as PET/CT, is essential for understanding biodistribution, improving safety, and optimizing the design of next-generation treatments. However, existing radiolabeling strategies for cell tracking using PET/CT lack the stability and sensitivity required for reliable long-term imaging. Here, we present a direct radiolabeling strategy that oxidizes cell surface sialic acids to conjugate aminooxy-DFO (AOD) and subsequently radiolabels cells with 89 Zr under biocompatible conditions. We radiolabeled five human and nonhuman primate immune cell types with high radiochemical incorporation (17–194 μCi per million cells) and purity (∼90%), while preserving cell viability. Serial PET/CT imaging over 7–8 days revealed conserved biodistribution patterns across all cell types tested. This approach provides a robust, applicable platform for longitudinal PET/CT tracking of therapeutic cells.

Journal of Medicinal Chemistry
University of Wisconsin–Madison (US), Medical College of Wisconsin (US), University of Wisconsin Carbone Cancer Center (US)
University of Wisconsin-Madison, University of Wisconsin Carbone Cancer Center, National Institutes of Health, School of Medicine and Public Health, University of Wisconsin-Madison, National Heart, Lung, and Blood Institute, NIH Office of the Director, National Cancer Institute, National Institute of General Medical Sciences
Good health and well-being
Openalex Percentile: Top 12%
Nanoplatforms for cancer theranostics
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