Abstract
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.
| Original language | English |
|---|---|
| Article number | e42662 |
| Journal | PLoS ONE |
| Volume | 7 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 6 Aug 2012 |
Authors (Note for portal: view the doc link for the full list of authors)
- Authors
- Treacy, O;Ryan, AE;Heinzl, T;O'Flynn, L;Cregg, M;Wilk, M;Odoardi, F;Lohan, P;O'Brien, T;Nosov, M;Ritter, T
- Treacy, O,Ryan, AE,Heinzl, T,OFlynn, L,Cregg, M,Wilk, M,Odoardi, F,Lohan, P,OBrien, T,Nosov, M,Ritter, T