Mesenchymal stem cells and autoimmune diseases

被引:127
作者
Dazzi, Francesco [1 ]
Krampera, Mauro [2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Haematol Ctr, Dept Med, London, England
[2] Univ Verona, Stem Cell Res Lab, Sect Hematol, Dept Med, I-37100 Verona, Italy
基金
英国医学研究理事会;
关键词
mesenchymal stem cells; autoimmune diseases; inflammation; cell therapy; VERSUS-HOST-DISEASE; SYSTEMIC-LUPUS-ERYTHEMATOSUS; COLLAGEN-INDUCED ARTHRITIS; ANTIGEN-PRESENTING CELL; PROLIFERATION IN-VITRO; MARROW STROMAL CELLS; REGULATORY T-CELLS; RHEUMATOID-ARTHRITIS; INTERFERON-GAMMA; IMMUNOSUPPRESSIVE PROPERTIES;
D O I
10.1016/j.beha.2011.01.002
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Mesenchymal stem cell (MSC) immunosuppressive properties offer a potentially attractive therapeutic modality for autoimmune diseases. MSC inhibit virtually all types of immune responses in vitro and prevent the induction of disease in several experimental models of autoimmunity. However, the processes involved in the pathogenesis of human diseases are more complicated and treatment cannot be administered before disease induction. In autoimmune diseases persistent antigenic stimulation recruits endogenous MSC to the site of lesion that contribute to the fibrotic evolution. Therefore, administering MSC to a chronic inflammatory disorder may not be desirable. In fact. MSC are not constitutively immunosuppressive but require a 'licensing' step provided by molecules of acute phase inflammation, like IFN gamma and TNF-alpha, or toll-like receptor (TLR) ligands. Conversely, different cytokines and/or the stimulation of selective TLR make MSC to become immunostimulatory. Therefore, dissecting the inflammatory environment in autoimmune diseases will identify the best conditions amenable to successful MSC therapy. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:49 / 57
页数:9
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