A Role for Mesenchymal Stem Cells in the Control of Graft-Versus-Host Disease

被引:8
作者
Cohen, Jose L. [1 ]
Sudres, Muriel [1 ]
机构
[1] Univ Paris 06, CNRS, UMR, F-75013 Paris, France
关键词
Graft versus host disease; Mesenchymal stem cells; Immunosuppression; Cell therapy; Allogeneic hematopoietic stem-cell transplantation; HEMATOLOGIC MALIGNANCY PATIENTS; BONE-MARROW TRANSPLANTATION; PROLIFERATION IN-VITRO; T-CELLS; STROMAL CELLS; COTRANSPLANTATION; INHIBIT; MICE;
D O I
10.1097/TP.0b013e3181a2876f
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Several reports have demonstrated the ability of mesenchymal stem cells (MSCs) to enhance hemopoietic engraftment and to exert a profound inhibitory effect on T-cell proliferation in vitro, making them a candidate for the prevention/treatment of graft-versus-host disease. Recent publications have highlighted the underlying mechanisms of the immunosuppressive function of MSCs, elicited by proinflammatory cytokines, such as interferon-gamma and tumor necrosis factor-alpha. These new findings have lead to a better understanding of the biology of MSCS, the outcome of graft-versus-host disease clinical trials and the conflicting results of preclinical T-cell-dependent pathologies. The potential use of MSCs as immunosuppressive elements in allogeneic stem-cell transplantation settings is thus discussed below.
引用
收藏
页码:S53 / S54
页数:2
相关论文
共 21 条
[1]
Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo [J].
Bartholomew, A ;
Sturgeon, C ;
Siatskas, M ;
Ferrer, K ;
McIntosh, K ;
Patil, S ;
Hardy, W ;
Devine, S ;
Ucker, D ;
Deans, R ;
Moseley, A ;
Hoffman, R .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (01) :42-48
[2]
CD4+CD25+ immunoregulatory T cells:: New therapeutics for graft-versus-host disease [J].
Cohen, JL ;
Trenado, A ;
Vasey, D ;
Klatzmann, D ;
Salomon, BL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (03) :401-406
[3]
Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli [J].
Di Nicola, M ;
Carlo-Stella, C ;
Magni, M ;
Milanesi, M ;
Longoni, PD ;
Matteucci, P ;
Grisanti, S ;
Gianni, AM .
BLOOD, 2002, 99 (10) :3838-3843
[4]
Reversal of the immunosuppressive properties of mesenchymal stem cells by tumor necrosis factor α in collagen-induced arthritis [J].
Djouad, F ;
Fritz, V ;
Apparailly, F ;
Louis-Plence, P ;
Bony, C ;
Sany, J ;
Jorgensen, C ;
Noël, D .
ARTHRITIS AND RHEUMATISM, 2005, 52 (05) :1595-1603
[5]
Immunosuppressive effect of mesenchymal stem cells favors tumor growth in allogeneic animals [J].
Djouad, F ;
Plence, P ;
Bony, C ;
Tropel, P ;
Apparailly, F ;
Sany, J ;
Noël, D ;
Jorgensen, C .
BLOOD, 2003, 102 (10) :3837-3844
[6]
Allogeneic marrow stromal cells are immune rejected by MHC class I- and class II-mismatched recipient mice [J].
Eliopoulos, N ;
Stagg, J ;
Lejeune, L ;
Pommey, S ;
Galipeau, J .
BLOOD, 2005, 106 (13) :4057-4065
[7]
HOROWITZ MM, 1990, BLOOD, V75, P555
[8]
Rapid hematopoietic recovery after coinfusion of autologous-blood stem cells and culture-expanded marrow mesenchymal stem cells in advanced breast cancer patients receiving high-dose chemotherapy [J].
Koç, ON ;
Gerson, SL ;
Cooper, BW ;
Dyhouse, SM ;
Haynesworth, SE ;
Caplan, AI ;
Lazarus, HM .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (02) :307-316
[9]
Bone marrow mesenchymal stem cells inhibit the response of naive and memory antigen-specific T cells to their cognate peptide [J].
Krampera, M ;
Glennie, S ;
Dyson, J ;
Scott, D ;
Laylor, R ;
Simpson, E ;
Dazzi, F .
BLOOD, 2003, 101 (09) :3722-3729
[10]
Cotransplantation of HLA-identical sibling culture-expanded mesenchymal stem cells and hematopoietic stem cells in hematologic malignancy patients [J].
Lazarus, HM ;
Koc, ON ;
Devine, SM ;
Curtin, P ;
Maziarz, RT ;
Holland, HK ;
Shpall, EJ ;
McCarthy, P ;
Atkinson, K ;
Cooper, BW ;
Gerson, SL ;
Laughlin, MJ ;
Loberiza, FR ;
Moseley, AB ;
Bacigalupo, A .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (05) :389-398