Mesenchymal stromal cells for tolerance induction in organ transplantation

被引:40
作者
Casiraghi, Federica [1 ]
Perico, Norberto [1 ]
Remuzzi, Giuseppe [1 ,2 ,3 ]
机构
[1] IRCCS Ist Ric Farmacol Mario Negri, Bergamo, Italy
[2] ASST, Unit Nephrol & Dialysis, Bergamo, Italy
[3] Univ Milan, L Sacco Dept Biomed & Clin Sci, Milan, Italy
基金
欧盟地平线“2020”;
关键词
Mesenchymal stromal cells; Kidney transplantation; Tolerance; Regulatory T cells; Memory T cells; REGULATORY T-CELLS; RABBIT ANTITHYMOCYTE GLOBULIN; ADULT PROGENITOR CELLS; STEM-CELLS; RENAL-TRANSPLANTATION; KIDNEY-TRANSPLANTATION; LONG-TERM; INDOLEAMINE 2,3-DIOXYGENASE; HOMEOSTATIC PROLIFERATION; IMMUNOSUPPRESSIVE DRUGS;
D O I
10.1016/j.humimm.2017.12.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The primary challenge in organ transplantation continues to be the need to suppress the host immune system long-term to ensure prolonged allograft survival. Long-term non-specific immunosuppression can, however, result in life-threatening complications. Thus, efforts have been pursued to explore novel strategies that would allow minimization of maintenance immunosuppression, eventually leading to transplant tolerance. In this scenario, bone marrow-derived mesenchymal stromal cells (MSC), given their unique inununomodulatory properties to skew the balance between regulatory and memory T cells, have emerged as potential candidates for cell-based therapy to promote immune tolerance. Here, we review our initial clinical experience with bone marrow-derived MSC in living-donor kidney transplant recipients and provide an overview of the available results of other clinical programs with MSC in kidney and liver transplantation, highlighting hurdles and success of this innovative cell-based therapy.
引用
收藏
页码:304 / 313
页数:10
相关论文
共 126 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Mesenchymal-Stem-Cell-Induced Immunoregulation Involves FAS-Ligand-/FAS-Mediated T Cell Apoptosis [J].
Akiyama, Kentaro ;
Chen, Chider ;
Wang, DanDan ;
Xu, Xingtian ;
Qu, Cunye ;
Yamaza, Takayoshi ;
Cai, Tao ;
Chen, WanJun ;
Sun, Lingyun ;
Shi, Songtao .
CELL STEM CELL, 2012, 10 (05) :544-555
[3]   Allo-HLA reactivity of virus-specific memory T cells is common [J].
Amir, Avital L. ;
D'Orsogna, Lloyd J. A. ;
Roelen, Dave L. ;
van Loenen, Marleen M. ;
Hagedoorn, Renate S. ;
de Boer, Renate ;
van der Hoorn, Menno A. W. G. ;
Kester, Michel G. D. ;
Doxiadis, Ilias I. N. ;
Falkenburg, J. H. Frederik ;
Claas, Frans H. J. ;
Heemskerk, Mirjam H. M. .
BLOOD, 2010, 115 (15) :3146-3157
[4]   Mesenchymal stem cells: immune evasive, not immune privileged [J].
Ankrum, James A. ;
Ong, Joon Faii ;
Karp, Jeffrey M. .
NATURE BIOTECHNOLOGY, 2014, 32 (03) :252-260
[5]   Pretransplant Antithymocyte Globulin Has Increased Efficacy in Controlling Donor-Reactive Memory T Cells in Mice [J].
Ayasoufi, K. ;
Yu, H. ;
Fan, R. ;
Wang, X. ;
Williams, J. ;
Valujskikh, A. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2013, 13 (03) :589-599
[6]   Murine bone marrow stromal progenitor cells elicit an in vivo cellular and humoral alloimmune response [J].
Badillo, Andrea T. ;
Beggs, Kirstin J. ;
Javazon, Elisabeth H. ;
Tebbets, Jessica C. ;
Flake, Alan W. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2007, 13 (04) :412-422
[7]   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
[8]  
Batsali AK, 2013, CURR STEM CELL RES T, V8, P144
[9]   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
[10]   Human mesenchymal stem cells alter antigen-presenting cell maturation and induce T-cell unresponsiveness [J].
Beyth, S ;
Borovsky, Z ;
Mevorach, D ;
Liebergall, M ;
Gazit, Z ;
Aslan, H ;
Galun, E ;
Rachmilewitz, J .
BLOOD, 2005, 105 (05) :2214-2219