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Therapeutic cell engineering using surface-conjugated synthetic nanoparticles

A major limitation of cell therapies is the rapid decline in viability and function of transplanted cells. Here we describe a strategy to enhance cell therapy via the conjugation of adjuvant drug-loaded nanoparticles to the surfaces of therapeutic cells. Using this method to provide sustained pseudo...

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Detalles Bibliográficos
Autores principales: Stephan, Matthias T., Moon, James J., Um, Soong Ho, Bershteyn, Anna, Irvine, Darrell J.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935928/
https://www.ncbi.nlm.nih.gov/pubmed/20711198
http://dx.doi.org/10.1038/nm.2198
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author Stephan, Matthias T.
Moon, James J.
Um, Soong Ho
Bershteyn, Anna
Irvine, Darrell J.
author_facet Stephan, Matthias T.
Moon, James J.
Um, Soong Ho
Bershteyn, Anna
Irvine, Darrell J.
author_sort Stephan, Matthias T.
collection PubMed
description A major limitation of cell therapies is the rapid decline in viability and function of transplanted cells. Here we describe a strategy to enhance cell therapy via the conjugation of adjuvant drug-loaded nanoparticles to the surfaces of therapeutic cells. Using this method to provide sustained pseudo-autocrine stimulation to donor cells, we elicited dramatic enhancements in tumor elimination in a model of adoptive T-cell therapy for cancer and increased the in vivo repopulation rate of hematopoietic stem cell grafts, using very low doses of adjuvant drugs that were ineffective when given systemically. This approach is a facile and generalizable strategy to augment cytoreagents while minimizing systemic side effects of adjuvant drugs. In addition, these results suggest therapeutic cells are promising vectors for actively targeted drug delivery.
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spelling pubmed-29359282011-03-01 Therapeutic cell engineering using surface-conjugated synthetic nanoparticles Stephan, Matthias T. Moon, James J. Um, Soong Ho Bershteyn, Anna Irvine, Darrell J. Nat Med Article A major limitation of cell therapies is the rapid decline in viability and function of transplanted cells. Here we describe a strategy to enhance cell therapy via the conjugation of adjuvant drug-loaded nanoparticles to the surfaces of therapeutic cells. Using this method to provide sustained pseudo-autocrine stimulation to donor cells, we elicited dramatic enhancements in tumor elimination in a model of adoptive T-cell therapy for cancer and increased the in vivo repopulation rate of hematopoietic stem cell grafts, using very low doses of adjuvant drugs that were ineffective when given systemically. This approach is a facile and generalizable strategy to augment cytoreagents while minimizing systemic side effects of adjuvant drugs. In addition, these results suggest therapeutic cells are promising vectors for actively targeted drug delivery. 2010-08-15 2010-09 /pmc/articles/PMC2935928/ /pubmed/20711198 http://dx.doi.org/10.1038/nm.2198 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Stephan, Matthias T.
Moon, James J.
Um, Soong Ho
Bershteyn, Anna
Irvine, Darrell J.
Therapeutic cell engineering using surface-conjugated synthetic nanoparticles
title Therapeutic cell engineering using surface-conjugated synthetic nanoparticles
title_full Therapeutic cell engineering using surface-conjugated synthetic nanoparticles
title_fullStr Therapeutic cell engineering using surface-conjugated synthetic nanoparticles
title_full_unstemmed Therapeutic cell engineering using surface-conjugated synthetic nanoparticles
title_short Therapeutic cell engineering using surface-conjugated synthetic nanoparticles
title_sort therapeutic cell engineering using surface-conjugated synthetic nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935928/
https://www.ncbi.nlm.nih.gov/pubmed/20711198
http://dx.doi.org/10.1038/nm.2198
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