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Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI

PURPOSE: Cellular therapeutics are emerging as a treatment option for a host of serious human diseases. To accelerate clinical translation, noninvasive imaging of cell grafts in clinical trials can potentially be used to assess the initial delivery and behavior of cells. METHODS: The use of a perflu...

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Autores principales: Ahrens, Eric T, Helfer, Brooke M, O'Hanlon, Charles F, Schirda, Claudiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253123/
https://www.ncbi.nlm.nih.gov/pubmed/25241945
http://dx.doi.org/10.1002/mrm.25454
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author Ahrens, Eric T
Helfer, Brooke M
O'Hanlon, Charles F
Schirda, Claudiu
author_facet Ahrens, Eric T
Helfer, Brooke M
O'Hanlon, Charles F
Schirda, Claudiu
author_sort Ahrens, Eric T
collection PubMed
description PURPOSE: Cellular therapeutics are emerging as a treatment option for a host of serious human diseases. To accelerate clinical translation, noninvasive imaging of cell grafts in clinical trials can potentially be used to assess the initial delivery and behavior of cells. METHODS: The use of a perfluorocarbon (PFC) tracer agent for clinical fluorine-19 ((19)F) MRI cell detection is described. This technology was used to detect immunotherapeutic dendritic cells (DCs) delivered to colorectal adenocarcinoma patients. Autologous DC vaccines were labeled with a PFC MRI agent ex vivo. Patients received DCs intradermally, and (19)F spin-density-weighted MRI at 3 Tesla (T) was used to observe cells. RESULTS: Spin-density-weighted (19)F images at the injection site displayed DCs as background-free “hot-spot” images. (19)F images were acquired in clinically relevant scan times (<10 min). Apparent DC numbers could be quantified in two patients from the (19)F hot-spots and were observed to decrease by ∼50% at injection site by 24 h. From 3T phantom studies, the sensitivity limit for DC detection is estimated to be on the order of ∼10(5) cells/voxel in this study. CONCLUSION: These results help to establish a clinically applicable means to track a broad range of cell types used in cell therapy. Magn Reson Med 72:1696–1701, 2014. © 2014 The Authors. Magnetic Resonance in Medicine Published by Wiley Periodicals, Inc. on behalf of International Society of Medicine in Resonance.
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spelling pubmed-42531232014-12-08 Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI Ahrens, Eric T Helfer, Brooke M O'Hanlon, Charles F Schirda, Claudiu Magn Reson Med Preclinical and Clinical Imaging—Rapid Communication PURPOSE: Cellular therapeutics are emerging as a treatment option for a host of serious human diseases. To accelerate clinical translation, noninvasive imaging of cell grafts in clinical trials can potentially be used to assess the initial delivery and behavior of cells. METHODS: The use of a perfluorocarbon (PFC) tracer agent for clinical fluorine-19 ((19)F) MRI cell detection is described. This technology was used to detect immunotherapeutic dendritic cells (DCs) delivered to colorectal adenocarcinoma patients. Autologous DC vaccines were labeled with a PFC MRI agent ex vivo. Patients received DCs intradermally, and (19)F spin-density-weighted MRI at 3 Tesla (T) was used to observe cells. RESULTS: Spin-density-weighted (19)F images at the injection site displayed DCs as background-free “hot-spot” images. (19)F images were acquired in clinically relevant scan times (<10 min). Apparent DC numbers could be quantified in two patients from the (19)F hot-spots and were observed to decrease by ∼50% at injection site by 24 h. From 3T phantom studies, the sensitivity limit for DC detection is estimated to be on the order of ∼10(5) cells/voxel in this study. CONCLUSION: These results help to establish a clinically applicable means to track a broad range of cell types used in cell therapy. Magn Reson Med 72:1696–1701, 2014. © 2014 The Authors. Magnetic Resonance in Medicine Published by Wiley Periodicals, Inc. on behalf of International Society of Medicine in Resonance. BlackWell Publishing Ltd 2014-12 2014-09-19 /pmc/articles/PMC4253123/ /pubmed/25241945 http://dx.doi.org/10.1002/mrm.25454 Text en © 2014 The Authors. Magnetic Resonance in Medicine Published by Wiley Periodicals, Inc. on behalf of International Society of Medicine in Resonance. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Preclinical and Clinical Imaging—Rapid Communication
Ahrens, Eric T
Helfer, Brooke M
O'Hanlon, Charles F
Schirda, Claudiu
Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI
title Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI
title_full Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI
title_fullStr Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI
title_full_unstemmed Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI
title_short Clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 MRI
title_sort clinical cell therapy imaging using a perfluorocarbon tracer and fluorine-19 mri
topic Preclinical and Clinical Imaging—Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253123/
https://www.ncbi.nlm.nih.gov/pubmed/25241945
http://dx.doi.org/10.1002/mrm.25454
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