Interactions Between Mesenchymal Stem Cells and Dendritic Cells

被引:35
|
作者
Spaggiari, Grazia Maria [1 ]
Moretta, Lorenzo [2 ]
机构
[1] Univ Genoa, Dept Expt Med, I-16132 Genoa, Italy
[2] Giannina Gaslini Inst, Sci Direct, I-16147 Genoa, Italy
关键词
DC cytoskeleton rearrangement; DC maturation; DC phenotype; Dendritic cell differentiation; Dendritic cells; Hematopoietic stem cell transplantation; Immune synapse; MSC licensing; MSC-mediated immunosuppression; Notch-2; PGE2; Tolerogenic DC; Treg cells; Unrestricted somatic stem cells; STROMAL CELLS; DIFFERENTIATION; TRANSPLANTATION; MATURATION; GENERATION; PATHWAY; DISEASE;
D O I
10.1007/10_2012_154
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem or stromal cells (MSC) are considered a promising new therapeutic strategy for the treatment of several pathological conditions. Due to their immunomodulatory properties, they are currently employed in clinical trials aimed at preventing or treating steroid-resistant acute graft-versus-host disease (GvHD), a frequent complication of allogeneic hematopoietic stem cell transplantation (HSCT). In addition, the use of MSC has been proposed for the treatment of autoimmune diseases. A number of recent studies have focused on the influence of MSC on dendritic cell (DC) function. DCs play a critical role in initiating and regulating immune responses by promoting antigen-specific T cell activation. Moreover, they are involved in efficient cross-talk with different cells of the innate immune system. DC are the most effective antigen-presenting cells and prime na T cells to initiate adaptive immune responses including those against allogeneic cells or self-antigens. Thus, alteration of DC generation or function may greatly contribute to the inhibition of T cell responses. In this context, MSC were shown to interfere with DC maturation from monocytes or CD34(+) hemopoietic precursors thus further confirming their role in immune regulation and their usefulness in cell-based therapies.
引用
收藏
页码:199 / 208
页数:10
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