Cargando…

Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process

Natural killer (NK) cell-based adoptive immunotherapy is a promising treatment approach for many cancers. However, development of protocols that provide large numbers of functional NK cells produced under GMP conditions are required to facilitate clinical studies. In this study, we translated our cy...

Descripción completa

Detalles Bibliográficos
Autores principales: Spanholtz, Jan, Preijers, Frank, Tordoir, Marleen, Trilsbeek, Carel, Paardekooper, Jos, de Witte, Theo, Schaap, Nicolaas, Dolstra, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116834/
https://www.ncbi.nlm.nih.gov/pubmed/21698239
http://dx.doi.org/10.1371/journal.pone.0020740
_version_ 1782206284456525824
author Spanholtz, Jan
Preijers, Frank
Tordoir, Marleen
Trilsbeek, Carel
Paardekooper, Jos
de Witte, Theo
Schaap, Nicolaas
Dolstra, Harry
author_facet Spanholtz, Jan
Preijers, Frank
Tordoir, Marleen
Trilsbeek, Carel
Paardekooper, Jos
de Witte, Theo
Schaap, Nicolaas
Dolstra, Harry
author_sort Spanholtz, Jan
collection PubMed
description Natural killer (NK) cell-based adoptive immunotherapy is a promising treatment approach for many cancers. However, development of protocols that provide large numbers of functional NK cells produced under GMP conditions are required to facilitate clinical studies. In this study, we translated our cytokine-based culture protocol for ex vivo expansion of NK cells from umbilical cord blood (UCB) hematopoietic stem cells into a fully closed, large-scale, cell culture bioprocess. We optimized enrichment of CD34(+) cells from cryopreserved UCB units using the CliniMACS system followed by efficient expansion for 14 days in gas-permeable cell culture bags. Thereafter, expanded CD34(+) UCB cells could be reproducibly amplified and differentiated into CD56(+)CD3(−) NK cell products using bioreactors with a mean expansion of more than 2,000 fold and a purity of >90%. Moreover, expansion in the bioreactor yielded a clinically relevant dose of NK cells (mean: 2×10(9) NK cells), which display high expression of activating NK receptors and cytolytic activity against K562. Finally, we established a versatile closed washing procedure resulting in optimal reduction of medium, serum and cytokines used in the cell culture process without changes in phenotype and cytotoxic activity. These results demonstrate that large numbers of UCB stem cell-derived NK cell products for adoptive immunotherapy can be produced in closed, large-scale bioreactors for the use in clinical trials.
format Online
Article
Text
id pubmed-3116834
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-31168342011-06-22 Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process Spanholtz, Jan Preijers, Frank Tordoir, Marleen Trilsbeek, Carel Paardekooper, Jos de Witte, Theo Schaap, Nicolaas Dolstra, Harry PLoS One Research Article Natural killer (NK) cell-based adoptive immunotherapy is a promising treatment approach for many cancers. However, development of protocols that provide large numbers of functional NK cells produced under GMP conditions are required to facilitate clinical studies. In this study, we translated our cytokine-based culture protocol for ex vivo expansion of NK cells from umbilical cord blood (UCB) hematopoietic stem cells into a fully closed, large-scale, cell culture bioprocess. We optimized enrichment of CD34(+) cells from cryopreserved UCB units using the CliniMACS system followed by efficient expansion for 14 days in gas-permeable cell culture bags. Thereafter, expanded CD34(+) UCB cells could be reproducibly amplified and differentiated into CD56(+)CD3(−) NK cell products using bioreactors with a mean expansion of more than 2,000 fold and a purity of >90%. Moreover, expansion in the bioreactor yielded a clinically relevant dose of NK cells (mean: 2×10(9) NK cells), which display high expression of activating NK receptors and cytolytic activity against K562. Finally, we established a versatile closed washing procedure resulting in optimal reduction of medium, serum and cytokines used in the cell culture process without changes in phenotype and cytotoxic activity. These results demonstrate that large numbers of UCB stem cell-derived NK cell products for adoptive immunotherapy can be produced in closed, large-scale bioreactors for the use in clinical trials. Public Library of Science 2011-06-16 /pmc/articles/PMC3116834/ /pubmed/21698239 http://dx.doi.org/10.1371/journal.pone.0020740 Text en Spanholtz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Spanholtz, Jan
Preijers, Frank
Tordoir, Marleen
Trilsbeek, Carel
Paardekooper, Jos
de Witte, Theo
Schaap, Nicolaas
Dolstra, Harry
Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process
title Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process
title_full Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process
title_fullStr Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process
title_full_unstemmed Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process
title_short Clinical-Grade Generation of Active NK Cells from Cord Blood Hematopoietic Progenitor Cells for Immunotherapy Using a Closed-System Culture Process
title_sort clinical-grade generation of active nk cells from cord blood hematopoietic progenitor cells for immunotherapy using a closed-system culture process
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3116834/
https://www.ncbi.nlm.nih.gov/pubmed/21698239
http://dx.doi.org/10.1371/journal.pone.0020740
work_keys_str_mv AT spanholtzjan clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT preijersfrank clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT tordoirmarleen clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT trilsbeekcarel clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT paardekooperjos clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT dewittetheo clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT schaapnicolaas clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess
AT dolstraharry clinicalgradegenerationofactivenkcellsfromcordbloodhematopoieticprogenitorcellsforimmunotherapyusingaclosedsystemcultureprocess