Potential of mesenchymal stem cells as immune therapy in solid-organ transplantation

被引:54
作者
Crop, Meindert [1 ]
Baan, Carla [1 ]
Weimar, Willem [1 ]
Hoogduijn, Martin [1 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Internal Med, Rotterdam, Netherlands
关键词
cell therapy; immune disease; immune modulation; immune therapy; mesenchymal stem cell; solid-organ transplantation; HUMAN BONE-MARROW; VERSUS-HOST-DISEASE; SUPPRESS T-LYMPHOCYTE; HUMAN ADIPOSE-TISSUE; STROMAL CELLS; IN-VITRO; INTERFERON-GAMMA; HUMAN HEART; CORD BLOOD; INHIBIT;
D O I
10.1111/j.1432-2277.2008.00786.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Over the last decade, there has been a rising interest in the use of mesenchymal stem cells (MSCs) for clinical applications. This interest stems from the beneficial properties of MSCs, which include multi-lineage differentiation and immunosuppressive ability, suggesting there is a role for MSC therapy for tissue regeneration and in immunologic disease. Despite recent clinical trials investigating the use of MSCs in treating immune-mediated disease, their applicability in solid-organ transplantation is still unknown. In this review, we identified topics that are important when considering MSC therapy in clinical organ transplantation. Whereas, from other clinical studies, it would appear that administration of MSCs is safe, issues like dosing, timing, route of administration, and in particular the use of autologous or donor-derived MSCs may be of crucial importance for the functional outcome of MSCs treatment in organ transplantation. We discuss these topics and assess the feasibility of MSCs therapy in organ transplantation.
引用
收藏
页码:365 / 376
页数:12
相关论文
共 121 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Cotransplantation of human stromal cell progenitors into preimmune fetal sheep results in early appearance of human donor cells in circulation and boosts cell levels in bone marrow at later time points after transplantation [J].
Almeida-Porada, G ;
Porada, CD ;
Tran, N ;
Zanjani, ED .
BLOOD, 2000, 95 (11) :3620-3627
[3]   Cartilage repair using an in vitro generated scaffold-free tissue-engineered construct derived from porcine synovial mesenchymal stem cells [J].
Ando, Wataru ;
Tateishi, Kosuke ;
Hart, David A. ;
Katakai, Daisuke ;
Tanaka, Yoshinari ;
Nakata, Ken ;
Hashimoto, Jun ;
Fujie, Hiromichi ;
Shino, Konsel ;
Yoshikawa, Hideki ;
Nakamura, Norimasa .
BIOMATERIALS, 2007, 28 (36) :5462-5470
[4]  
Angoulvant D, 2004, BIORHEOLOGY, V41, P469
[5]   Cell therapy using allogeneic bone marrow mesenchymal stem cells prevents tissue damage in collagen-induced arthritis [J].
Augello, Andrea ;
Tasso, Roberta ;
Negrini, Simone Maria ;
Cancedda, Ranieri ;
Pennesi, Giuseppina .
ARTHRITIS AND RHEUMATISM, 2007, 56 (04) :1175-1186
[6]   Cotransplantation of ex vivo-expanded mesenchymal stem cells accelerates lymphocyte recovery and may reduce the risk of graft failure in haploidentical hematopoietic stem-cell transplantation [J].
Ball, Lynne M. ;
Bernardo, Maria Ester ;
Roelofs, Helene ;
Lankester, Arjan ;
Cometa, Angela ;
Egeler, R. Maarten ;
Locatelli, Franco ;
Fibbe, Willem E. .
BLOOD, 2007, 110 (07) :2764-2767
[7]   Immunogenicity of adult mesenchymal stem cells: Lessons from the fetal allograft [J].
Barry, FP ;
Murphy, JM ;
English, K ;
Mahon, BP .
STEM CELLS AND DEVELOPMENT, 2005, 14 (03) :252-265
[8]   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
[9]   Human mesenchymal stem cells induce T cell anergy and downregulate T cell allo-responses via the TH2 pathway: Relevance to tissue engineering human heart valves [J].
Batten, Puspa ;
Sarathchandra, Padmini ;
Antoniw, Joseph W. ;
Tay, Szun Szun ;
Lowdell, Mark W. ;
Taylor, Patricia M. ;
Yacoub, Magdi H. .
TISSUE ENGINEERING, 2006, 12 (08) :2263-2273
[10]   Immunologic consequences of multiple, high-dose administration of allogeneic mesenchymal stem cells to baboons [J].
Beggs, Kirstin J. ;
Lyubimov, Alex ;
Borneman, Jade N. ;
Bartholomew, Amelia ;
Moseley, Annemarie ;
Dodds, Robert ;
Archambault, Michael P. ;
Smith, Alan K. ;
McIntosh, Kevin R. .
CELL TRANSPLANTATION, 2006, 15 (8-9) :711-721