Adenoviral Transduction of Mesenchymal Stem Cells: In Vitro Responses and In Vivo Immune Responses after Cell Transplantation

被引:30
|
作者
Treacy, Oliver [1 ]
Ryan, Aideen E. [1 ]
Heinzl, Teresa [1 ]
O'Flynn, Lisa [1 ]
Cregg, Marese [1 ]
Wilk, Mieszko [1 ]
Odoardi, Francesca [2 ]
Lohan, Paul [1 ]
O'Brien, Timothy [1 ]
Nosov, Mikhail [1 ]
Ritter, Thomas [1 ]
机构
[1] Natl Univ Ireland, Regenerat Med Inst, Sch Med, Coll Med Nursing & Hlth Sci, Galway, Ireland
[2] Univ Med, Dept Neuroimmunol, Inst Multiple Sclerosis Res, Gottingen, Germany
来源
PLOS ONE | 2012年 / 7卷 / 08期
基金
爱尔兰科学基金会;
关键词
FUNCTIONAL CHEMOKINE RECEPTORS; MEDIATED GENE-TRANSFER; STROMAL CELLS; DENDRITIC CELLS; ENGRAFTMENT; MIGRATION; THERAPY; VECTORS; MODULATION; EXPRESSION;
D O I
10.1371/journal.pone.0042662
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:13
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