Therapeutic Potential of Mesenchymal Stem Cells in Immune-Mediated Diseases

被引:15
|
作者
Eljarrah, Adam [1 ,2 ]
Gergues, Marina [1 ,2 ]
Pobiarzyn, Piotr W. [1 ,2 ]
Sandiford, Oleta A. [1 ,2 ]
Rameshwar, Pranela [3 ]
机构
[1] Rutgers New Jersey Med Sch, Dept Med, Newark, NJ USA
[2] Univ Med & Dent New Jersey, Grad Sch, Rutgers Sch, Newark, NJ USA
[3] Rutgers Sch Biomed Hlth Sci, New Jersey Med Sch, Dept Med, Div Hematol Oncol, Newark, NJ 07107 USA
来源
关键词
Mesenchymal stem cells; Cytokines; Cell therapy; Drug delivery; Immune response; Graft-versus-host response; REGULATORY T-CELLS; MARROW STROMAL CELLS; VERSUS-HOST-DISEASE; B-CELLS; INDOLEAMINE 2,3-DIOXYGENASE; DENDRITIC CELLS; MURINE MODEL; INHIBIT; PROLIFERATION; DIFFERENTIATION;
D O I
10.1007/978-3-030-31206-0_5
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells (MSCs) are multipotent cells that can self--renew and differentiate into cells of all germ layers. MSCs can be easily attracted to the site of tissue insult with high levels of inflammatory mediators. The general ability of MSCs to migrate at the sites of tissue injury suggested an innate ability for these cells to be involved in baseline tissue repair. The bone marrow is one of the primary sources of MSCs, though they can be ubiquitous. An attractive property of MSCs for clinical application is their ability to cross allogeneic barrier. However, alone, MSCs are not immune suppressive cells. Rather, they can be licensed by the tissue microenvironment to become immune suppressor cells. Immune suppressor functions of MSCs include those that blunt cytotoxicity of natural killer cells, suppression of T-cell proliferation, and "veto" function. MSCs, as third-party cells, suppress the immune response that generally recapitulates graft-versus-host disease (GvHD) responses. Based on the plastic functions of MSCs, these cells have dominated the field of cell-based therapies, such as anti-inflammatory and drug delivery. Here, we focus on the potential use of MSC for immunological disorders such as Crohn's disease and GvHD.
引用
收藏
页码:93 / 108
页数:16
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