Volume 129, Issue 2 pp. 365-373
Tumor Immunology

A novel 19F agent for detection and quantification of human dendritic cells using magnetic resonance imaging

Fernando Bonetto

Fernando Bonetto

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

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Mangala Srinivas

Mangala Srinivas

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

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Arend Heerschap

Arend Heerschap

Department of Radiology, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

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Robbie Mailliard

Robbie Mailliard

Celsense Inc., Pittsburgh, PA

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Eric T. Ahrens

Eric T. Ahrens

Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA

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Carl G. Figdor

Carl G. Figdor

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

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I. Jolanda M. de Vries

Corresponding Author

I. Jolanda M. de Vries

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

Tel.: 31-3617600, Fax: 31-24-3540339

Department of Tumor Immunology, Radboud University Nijmegen Medical Center, P.O. Box 9101, 6500 HB Nijmegen, NetherlandsSearch for more papers by this author
First published: 13 September 2010
Citations: 61

Abstract

Monitoring of cell therapeutics in vivo is of major importance to estimate its efficacy. Here, we present a novel intracellular label for 19F magnetic resonance imaging (MRI)-based cell tracking, which allows for noninvasive, longitudinal cell tracking without the use of radioisotopes. A key advantage of 19F MRI is that it allows for absolute quantification of cell numbers directly from the MRI data. The 19F label was tested in primary human monocyte-derived dendritic cells. These cells took up label effectively, resulting in a labeling of 1.7 ± 0.1 × 1013 19F atoms per cell, with a viability of 80 ± 6%, without the need for electroporation or transfection agents. This results in a minimum detection sensitivity of about 2,000 cells/voxel at 7 T, comparable with gadolinium-labeled cells. Comparison of the detection sensitivity of cells labeled with 19F, iron oxide and gadolinium over typical tissue background showed that unambiguous detection of the 19F-labeled cells was simpler than with the contrast agents. The effect of the 19F agent on cell function was minimal in the context of cell-based vaccines. From these data, we calculate that detection of 30,000 cells in vivo at 3 T with a reasonable signal to noise ratio for 19F images would require less than 30 min with a conventional fast spin echo sequence, given a coil similar to the one used in this study. This is well within acceptable limits for clinical studies, and thus, we conclude that 19F MRI for quantitative cell tracking in a clinical setting has great potential.

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