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Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents
Genetically-modified T cells expressing chimeric antigen receptors (CAR) exert anti-tumor effect by identifying tumor-associated antigen (TAA), independent of major histocompatibility complex. For maximal efficacy and safety of adoptively transferred cells, imaging their biodistribution is critical....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968458/ https://www.ncbi.nlm.nih.gov/pubmed/24675806 http://dx.doi.org/10.1038/srep04502 |
_version_ | 1782309160619081728 |
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author | Bhatnagar, Parijat Alauddin, Mian Bankson, James A. Kirui, Dickson Seifi, Payam Huls, Helen Lee, Dean A. Babakhani, Aydin Ferrari, Mauro Li, King C. Cooper, Laurence J. N. |
author_facet | Bhatnagar, Parijat Alauddin, Mian Bankson, James A. Kirui, Dickson Seifi, Payam Huls, Helen Lee, Dean A. Babakhani, Aydin Ferrari, Mauro Li, King C. Cooper, Laurence J. N. |
author_sort | Bhatnagar, Parijat |
collection | PubMed |
description | Genetically-modified T cells expressing chimeric antigen receptors (CAR) exert anti-tumor effect by identifying tumor-associated antigen (TAA), independent of major histocompatibility complex. For maximal efficacy and safety of adoptively transferred cells, imaging their biodistribution is critical. This will determine if cells home to the tumor and assist in moderating cell dose. Here, T cells are modified to express CAR. An efficient, non-toxic process with potential for cGMP compliance is developed for loading high cell number with multi-modal (PET-MRI) contrast agents (Super Paramagnetic Iron Oxide Nanoparticles – Copper-64; SPION-(64)Cu). This can now be potentially used for (64)Cu-based whole-body PET to detect T cell accumulation region with high-sensitivity, followed by SPION-based MRI of these regions for high-resolution anatomically correlated images of T cells. CD19-specific-CAR(+)SPION(pos) T cells effectively target in vitro CD19(+) lymphoma. |
format | Online Article Text |
id | pubmed-3968458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39684582014-03-28 Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents Bhatnagar, Parijat Alauddin, Mian Bankson, James A. Kirui, Dickson Seifi, Payam Huls, Helen Lee, Dean A. Babakhani, Aydin Ferrari, Mauro Li, King C. Cooper, Laurence J. N. Sci Rep Article Genetically-modified T cells expressing chimeric antigen receptors (CAR) exert anti-tumor effect by identifying tumor-associated antigen (TAA), independent of major histocompatibility complex. For maximal efficacy and safety of adoptively transferred cells, imaging their biodistribution is critical. This will determine if cells home to the tumor and assist in moderating cell dose. Here, T cells are modified to express CAR. An efficient, non-toxic process with potential for cGMP compliance is developed for loading high cell number with multi-modal (PET-MRI) contrast agents (Super Paramagnetic Iron Oxide Nanoparticles – Copper-64; SPION-(64)Cu). This can now be potentially used for (64)Cu-based whole-body PET to detect T cell accumulation region with high-sensitivity, followed by SPION-based MRI of these regions for high-resolution anatomically correlated images of T cells. CD19-specific-CAR(+)SPION(pos) T cells effectively target in vitro CD19(+) lymphoma. Nature Publishing Group 2014-03-28 /pmc/articles/PMC3968458/ /pubmed/24675806 http://dx.doi.org/10.1038/srep04502 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported license. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Bhatnagar, Parijat Alauddin, Mian Bankson, James A. Kirui, Dickson Seifi, Payam Huls, Helen Lee, Dean A. Babakhani, Aydin Ferrari, Mauro Li, King C. Cooper, Laurence J. N. Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents |
title | Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents |
title_full | Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents |
title_fullStr | Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents |
title_full_unstemmed | Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents |
title_short | Tumor Lysing Genetically Engineered T Cells Loaded with Multi-Modal Imaging Agents |
title_sort | tumor lysing genetically engineered t cells loaded with multi-modal imaging agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968458/ https://www.ncbi.nlm.nih.gov/pubmed/24675806 http://dx.doi.org/10.1038/srep04502 |
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