| Literature DB >> 20619400 |
Mehdi Najar1, Gordana Raicevic, Hicham Id Boufker, Hussein Fayyad Kazan, Cécile De Bruyn, Nathalie Meuleman, Dominique Bron, Michel Toungouz, Laurence Lagneaux.
Abstract
Due to their immunomodulatory properties, adipose tissue (AT) and Wharton's Jelly (WJ) constitute valuable alternatives to BM as sources of MSCs for managing graft-versus-host disease. To ensure the efficiency of AT- and WJ-MSCs implies the characterization of their immunomodulatory functions in comparison to those of BM. In this study, we investigated the capacity of AT- and WJ-MSCs to modulate lymphocyte reactions in response to different stimuli as well as the specificity of this immunomodulation. AT- and WJ-MSC displayed potent immunosuppressive effects on lymphocyte responses in a dose-dependent manner. These effects included the prevention of lymphocyte activation as well as the suppression of T-cell proliferation regardless of the stimuli used to activate lymphocytes. These effects were mediated through the expression of COX1/COX2 enzymes and by the production of PGE2. CD4(+) and CD8(+) T-lymphocytes were equally targeted by MSCs demonstrating that the immunomodulation was not restricted to a specific T-cell subpopulation. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20619400 DOI: 10.1016/j.cellimm.2010.06.006
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868