Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.

Adult mesenchymal stem cells (MSCs) are non-hematopoietic cells with multi-lineage potential which makes them attractive targets for regenerative medicine applications. However, to date, therapeutic success of MSC-therapy is limited and the genetic modification of MSCs using viral vectors is one opt...

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Autores principales: Oliver Treacy, Aideen E Ryan, Teresa Heinzl, Lisa O'Flynn, Marese Cregg, Mieszko Wilk, Francesca Odoardi, Paul Lohan, Timothy O'Brien, Mikhail Nosov, Thomas Ritter
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:55d431c8d85e47059b111fe8ebca52512021-11-18T07:09:32ZAdenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.1932-620310.1371/journal.pone.0042662https://doaj.org/article/55d431c8d85e47059b111fe8ebca52512012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22880073/?tool=EBIhttps://doaj.org/toc/1932-6203Adult mesenchymal stem cells (MSCs) are non-hematopoietic cells with multi-lineage potential which makes them attractive targets for regenerative medicine applications. However, to date, therapeutic success of MSC-therapy is limited and the genetic modification of MSCs using viral vectors is one option to improve their therapeutic potential. Ex-vivo genetic modification of MSCs using recombinant adenovirus (Ad) could be promising to reduce undesired immune responses as Ad will be removed before cell/tissue transplantation. In this regard, we investigated whether Ad-modification of MSCs alters their immunological properties in vitro and in vivo. We found that Ad-transduction of MSCs does not lead to up-regulation of major histocompatibility complex class I and II and co-stimulatory molecules CD80 and CD86. Moreover, Ad-transduction caused no significant changes in terms of pro-inflammatory cytokine expression, chemokine and chemokine receptor and Toll-like receptor expression. In addition, Ad-modification of MSCs had no affect on their ability to suppress T cell proliferation in vitro. In vivo injection of Ad-transduced MSCs did not change the frequency of various immune cell populations (antigen presenting cells, T helper and cytotoxic T cells, natural killer and natural killer T cells) neither in the blood nor in tissues. Our results indicate that Ad-modification has no major influence on the immunological properties of MSCs and therefore can be considered as a suitable gene vector for therapeutic applications of MSCs.Oliver TreacyAideen E RyanTeresa HeinzlLisa O'FlynnMarese CreggMieszko WilkFrancesca OdoardiPaul LohanTimothy O'BrienMikhail NosovThomas RitterPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 8, p e42662 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Oliver Treacy
Aideen E Ryan
Teresa Heinzl
Lisa O'Flynn
Marese Cregg
Mieszko Wilk
Francesca Odoardi
Paul Lohan
Timothy O'Brien
Mikhail Nosov
Thomas Ritter
Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
description Adult mesenchymal stem cells (MSCs) are non-hematopoietic cells with multi-lineage potential which makes them attractive targets for regenerative medicine applications. However, to date, therapeutic success of MSC-therapy is limited and the genetic modification of MSCs using viral vectors is one option to improve their therapeutic potential. Ex-vivo genetic modification of MSCs using recombinant adenovirus (Ad) could be promising to reduce undesired immune responses as Ad will be removed before cell/tissue transplantation. In this regard, we investigated whether Ad-modification of MSCs alters their immunological properties in vitro and in vivo. We found that Ad-transduction of MSCs does not lead to up-regulation of major histocompatibility complex class I and II and co-stimulatory molecules CD80 and CD86. Moreover, Ad-transduction caused no significant changes in terms of pro-inflammatory cytokine expression, chemokine and chemokine receptor and Toll-like receptor expression. In addition, Ad-modification of MSCs had no affect on their ability to suppress T cell proliferation in vitro. In vivo injection of Ad-transduced MSCs did not change the frequency of various immune cell populations (antigen presenting cells, T helper and cytotoxic T cells, natural killer and natural killer T cells) neither in the blood nor in tissues. Our results indicate that Ad-modification has no major influence on the immunological properties of MSCs and therefore can be considered as a suitable gene vector for therapeutic applications of MSCs.
format article
author Oliver Treacy
Aideen E Ryan
Teresa Heinzl
Lisa O'Flynn
Marese Cregg
Mieszko Wilk
Francesca Odoardi
Paul Lohan
Timothy O'Brien
Mikhail Nosov
Thomas Ritter
author_facet Oliver Treacy
Aideen E Ryan
Teresa Heinzl
Lisa O'Flynn
Marese Cregg
Mieszko Wilk
Francesca Odoardi
Paul Lohan
Timothy O'Brien
Mikhail Nosov
Thomas Ritter
author_sort Oliver Treacy
title Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
title_short Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
title_full Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
title_fullStr Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
title_full_unstemmed Adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
title_sort adenoviral transduction of mesenchymal stem cells: in vitro responses and in vivo immune responses after cell transplantation.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/55d431c8d85e47059b111fe8ebca5251
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