Mesenchymal stem cells for clinical application

被引:230
作者
Sensebe, L. [1 ,2 ]
Krampera, M. [3 ]
Schrezenmeier, H. [4 ,5 ]
Bourin, P.
Giordano, R. [6 ]
机构
[1] EFS Etab Francais Sang, GECSoM, Ctr Atlantique, F-37206 Tours 3, France
[2] Univ Tours, EA3855, Tours, France
[3] Univ Verona, Dept Clin & Expt Med, Sect Hematol, I-37100 Verona, Italy
[4] Univ Ulm, Inst Clin Transfus Med & Immunogenet, German Red Cross Blood Serv Baden Wurttemberg Hes, Ulm, Germany
[5] Univ Ulm, Inst Transfus Med, Ulm, Germany
[6] Fdn Osped Maggiore Policlin, Ctr Transfus Med Cellular Therapy & Cryobiol, Cell Factory F Calori, Milan, Italy
关键词
Mesenchymal Stem; Stromal Cells; immune intervention; regenerative medicine; GMP; MARROW STROMAL CELLS; VERSUS-HOST-DISEASE; HEMATOLOGIC MALIGNANCY PATIENTS; UMBILICAL-CORD BLOOD; HUMAN ADIPOSE-TISSUE; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; SUPPRESS T-LYMPHOCYTE; REFRACTORY ACUTE GVHD; PLATELET-RICH PLASMA; NATURAL-KILLER-CELLS;
D O I
10.1111/j.1423-0410.2009.01227.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mesenchymal Stem Cells/Multipotent Marrow Stromal Cells (MSC) are multipotent adult stem cells present in all tissues, as part of the perivascular population. As multipotent cells, MSCs can differentiate into different tissues originating from mesoderm ranging from bone and cartilage, to cardiac muscle. Conflicting data show that MSCs could be pluripotent and able to differentiate into tissues and cells of non-mesodermic origin as neurons or epithelial cells. Moreover, MSCs exhibit non-HLA restricted immunosuppressive properties. This wide range of properties leads to increasing uses of MSC for immunomodulation or tissue repair. Based on their immunosuppressive properties MSC are used particularly in the treatment of graft versus host disease, For tissue repair, MSCs can work by different ways from cell replacement to paracrine effects through the release of cytokines and to regulation of immune/inflammatory responses. In regenerative medicine, trials are in progress or planed for healing/repair of different tissue or organs as bone, cartilage, vessels, myocardium, or epithelia. Although it has been demonstrated that ex-vivo expansion processes using fetal bovine serum, recombinant growth factors (e.g. FGF2) or platelet lysate are feasible, definitive standards to produce clinical-grade MSC are still lacking. MSCs have to be produced according GMP and regulation constraints. For answering to the numerous challenges in this fast developing field of biology and medicine, integrative networks linking together research teams, cell therapy laboratories and clinical teams are needed.
引用
收藏
页码:93 / 107
页数:15
相关论文
共 138 条
[61]   Transplanted mesenchymal stem cells accelerate glomerular healing in experimental glomerulonephritis [J].
Kunter, Uta ;
Rong, Song ;
Djuric, Zivka ;
Boor, Peter ;
Muller-Newen, Gerhard ;
Yu, Donghai ;
Floege, Jurgen .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (08) :2202-2212
[62]   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
[63]   Transplantation of mesenchymal stem cells to enhance engraftment of hematopoietic stem cells [J].
Le Blanc, K. ;
Samuelsson, H. ;
Gustafsson, B. ;
Remberger, M. ;
Sundberg, B. ;
Arvidson, J. ;
Ljungman, P. ;
Lonnies, H. ;
Nava, S. ;
Ringden, O. .
LEUKEMIA, 2007, 21 (08) :1733-1738
[64]   Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells [J].
Le Blanc, K ;
Rasmusson, I ;
Sundberg, B ;
Götherström, C ;
Hassan, M ;
Uzunel, M ;
Ringdén, O .
LANCET, 2004, 363 (9419) :1439-1441
[65]   Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease:: a phase II study [J].
LeBlanc, Katarina ;
Frassoni, Francesco ;
Ball, Lynne ;
Locatelli, Franco ;
Roelofs, Helene ;
Lewis, Ian ;
Lanino, Edoardo ;
Sundberg, Berit ;
Bernardo, Maria Ester ;
Remberger, Mats ;
Dini, Giorgio ;
Egeler, R. Maarten ;
Bacigalupo, Andrea ;
Fibbe, Willem ;
Ringden, Olle .
LANCET, 2008, 371 (9624) :1579-1586
[66]   Embryonic origin and Hox status determine progenitor cell fate during adult bone regeneration [J].
Leucht, Philipp ;
Kim, Jae-Beom ;
Amasha, Raimy ;
James, Aaron W. ;
Girod, Sabine ;
Helms, Jill A. .
DEVELOPMENT, 2008, 135 (17) :2845-2854
[67]   Human mesenchymal stem cells engraft and demonstrate site-specific differentiation after in utero transplantation in sheep [J].
Liechty, KW ;
MacKenzie, TC ;
Shaaban, AF ;
Radu, A ;
Moseley, AB ;
Deans, R ;
Marshak, DR ;
Flake, AW .
NATURE MEDICINE, 2000, 6 (11) :1282-1286
[68]   Toll-like receptors 3 and 4 are expressed by human bone marrow-derived mesenchymal stem cells and can inhibit their T-cell modulatory activity by impairing notch signaling [J].
Liotta, Francesco ;
Angeli, Roberta ;
Cosmi, Lorenzo ;
Fili, Lucia ;
Manuelli, Cinzia ;
Frosali, Francesca ;
Mazzinghi, Benedetta ;
Maggi, Laura ;
Pasini, Annalisa ;
Lisi, Veronica ;
Santarlasci, Veronica ;
Consoloni, Lara ;
Angelotti, Maria Lucia ;
Romagnani, Paola ;
Parronchi, Paola ;
Krampera, Mauro ;
Maggi, Enrico ;
Romagnani, Sergio ;
Annunziato, Francesco .
STEM CELLS, 2008, 26 (01) :279-289
[69]   Induction of bone marrow stromal cells to neurons: Differentiation, transdifferentiation, or artifact? [J].
Lu, P ;
Blesch, A ;
Tuszynski, MH .
JOURNAL OF NEUROSCIENCE RESEARCH, 2004, 77 (02) :174-191
[70]   Reconstruction of chemically burned rat corneal surface by bone marrow-derived human mesenchymal stem cells [J].
Ma, Yanling ;
Xu, Yongsheng ;
Xiao, Zhifeng ;
Yang, Wei ;
Zhang, Chun ;
Song, E. ;
Du, Yiqin ;
Li, Lingsong .
STEM CELLS, 2006, 24 (02) :315-321