Human Mesenchymal Stem Cells and Immunosuppressive Drug Interactions in Allogeneic Responses: An In Vitro Study Using Human Cells

被引:68
作者
Buron, F. [1 ,2 ]
Perrin, H. [1 ,2 ]
Malcus, C. [3 ]
Hequet, O. [2 ]
Thaunat, O. [1 ,2 ]
Kholopp-Sarda, M. -N. [3 ]
Moulin, F. T. [3 ]
Morelon, E. [1 ,2 ]
机构
[1] Hop Edouard Herriot, Serv Nephrol Transplantat & Immunol Clin, Hosp Civils Lyon, F-69437 Lyon, France
[2] Univ Lyon 1, INSERM, U Lyon 851, F-69622 Villeurbanne, France
[3] Hop Edouard Herriot, Clin Immunol Lab, F-69437 Lyon, France
关键词
MARROW STROMAL CELLS; SUPPRESS T-LYMPHOCYTE; PROLIFERATION; INHIBIT; RAT; CYCLOSPORINE; THERAPY; HOST;
D O I
10.1016/j.transproceed.2009.08.030
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives. The use of mesenchymal stem cells (MSC), which display immunosuppressive activity, seems to be a promising therapeutic approach in solid organ transplantation. However, little is known about their interactions with immunosuppressive drugs. The objective of this study was to assess these interactions in allogeneic responses. Methods. We studied the effects on alloiramune responses in mixed lymphocyte reactions of MSC plus five agents-cyclosporine, tacrolimus, rapamycin, mycophenolate acid (MPA), and dexamethasone (DEX). Results. Human MSC isolated from bone marrow were characterized by their phenotype and their ability to differentiate into adipocytes or osteoblastes. MSC plus the agents inhibited allogeneic lymphocyte proliferation in a dose-dependent manner. Calcineurin inhibitors and rapamycin antagonized the inhibitory effect of MSC, whereas MPA promoted it and DXM did not modify it. Conclusion. MPA seems to be the best immunosuppressant to associated with MSC for transplanted patients.
引用
收藏
页码:3347 / 3352
页数:6
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