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All-in-one processing of heterogeneous human cell grafts for gene and cell therapy

Current cell processing technologies for gene and cell therapies are often slow, expensive, labor intensive and are compromised by high cell losses and poor selectivity thus limiting the efficacy and availability of clinical cell therapies. We employ cell-specific on-demand mechanical intracellular...

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Autores principales: Lukianova-Hleb, Ekaterina Y, Yvon, Eric S, Shpall, Elizabeth J, Lapotko, Dmitri O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793805/
https://www.ncbi.nlm.nih.gov/pubmed/27006970
http://dx.doi.org/10.1038/mtm.2016.12
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author Lukianova-Hleb, Ekaterina Y
Yvon, Eric S
Shpall, Elizabeth J
Lapotko, Dmitri O
author_facet Lukianova-Hleb, Ekaterina Y
Yvon, Eric S
Shpall, Elizabeth J
Lapotko, Dmitri O
author_sort Lukianova-Hleb, Ekaterina Y
collection PubMed
description Current cell processing technologies for gene and cell therapies are often slow, expensive, labor intensive and are compromised by high cell losses and poor selectivity thus limiting the efficacy and availability of clinical cell therapies. We employ cell-specific on-demand mechanical intracellular impact from laser pulse-activated plasmonic nanobubbles (PNB) to process heterogeneous human cell grafts ex vivo with dual simultaneous functionality, the high cell type specificity, efficacy and processing rate for transfection of target CD3+ cells and elimination of subsets of unwanted CD25+ cells. The developed bulk flow PNB system selectively processed human cells at a rate of up to 100 million cell/minute, providing simultaneous transfection of CD3+ cells with the therapeutic gene (FKBP12(V36)-p30Caspase9) with the efficacy of 77% and viability 95% (versus 12 and 60%, respectively, for standard electroporation) and elimination of CD25+ cells with 99% efficacy. PNB flow technology can unite and replace several methodologies in an all-in-one universal ex vivo simultaneous procedure to precisely and rapidly prepare a cell graft for therapy. PNB’s can process various cell systems including cord blood, stem cells, and bone marrow.
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spelling pubmed-47938052016-03-22 All-in-one processing of heterogeneous human cell grafts for gene and cell therapy Lukianova-Hleb, Ekaterina Y Yvon, Eric S Shpall, Elizabeth J Lapotko, Dmitri O Mol Ther Methods Clin Dev Article Current cell processing technologies for gene and cell therapies are often slow, expensive, labor intensive and are compromised by high cell losses and poor selectivity thus limiting the efficacy and availability of clinical cell therapies. We employ cell-specific on-demand mechanical intracellular impact from laser pulse-activated plasmonic nanobubbles (PNB) to process heterogeneous human cell grafts ex vivo with dual simultaneous functionality, the high cell type specificity, efficacy and processing rate for transfection of target CD3+ cells and elimination of subsets of unwanted CD25+ cells. The developed bulk flow PNB system selectively processed human cells at a rate of up to 100 million cell/minute, providing simultaneous transfection of CD3+ cells with the therapeutic gene (FKBP12(V36)-p30Caspase9) with the efficacy of 77% and viability 95% (versus 12 and 60%, respectively, for standard electroporation) and elimination of CD25+ cells with 99% efficacy. PNB flow technology can unite and replace several methodologies in an all-in-one universal ex vivo simultaneous procedure to precisely and rapidly prepare a cell graft for therapy. PNB’s can process various cell systems including cord blood, stem cells, and bone marrow. Nature Publishing Group 2016-03-16 /pmc/articles/PMC4793805/ /pubmed/27006970 http://dx.doi.org/10.1038/mtm.2016.12 Text en Copyright © 2016 Official journal of the American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Lukianova-Hleb, Ekaterina Y
Yvon, Eric S
Shpall, Elizabeth J
Lapotko, Dmitri O
All-in-one processing of heterogeneous human cell grafts for gene and cell therapy
title All-in-one processing of heterogeneous human cell grafts for gene and cell therapy
title_full All-in-one processing of heterogeneous human cell grafts for gene and cell therapy
title_fullStr All-in-one processing of heterogeneous human cell grafts for gene and cell therapy
title_full_unstemmed All-in-one processing of heterogeneous human cell grafts for gene and cell therapy
title_short All-in-one processing of heterogeneous human cell grafts for gene and cell therapy
title_sort all-in-one processing of heterogeneous human cell grafts for gene and cell therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793805/
https://www.ncbi.nlm.nih.gov/pubmed/27006970
http://dx.doi.org/10.1038/mtm.2016.12
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