Characterization of mesenchymal stromal cells: potency assay development

被引:24
作者
Hematti, Peiman [1 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Carbone Canc Ctr, Dept Med, Madison, WI 53705 USA
关键词
CRITERIA; STEM;
D O I
10.1111/trf.13569
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Based on their many different mechanisms of action, presumed immune-privileged status, and relative ease of production, mesenchymal stromal cells (MSCs) are under intensive clinical investigation for treating a wide range of degenerative, inflammatory, and immunologic disorders. Identification of relevant and robust potency assays is not only a regulatory requirement, but it is also the basis for producing and delivering a product that is consistent, safe, and ultimately an effective therapy. Although development of an appropriate potency assay is one of the most challenging issues in cell-based therapies, it is of paramount importance in the process of developing and testing cellular products. Regardless of the many different tissue sources and methods used in culture expansion of MSCs, they possess many of the same morphologic, cell surface markers, and differentiation characteristics. However, MSC products with similar phenotypic characteristics could still have major differences in their biologic and functional attributes. Understanding the different mechanisms of action and establishment of relevant potency assays is of pivotal importance in allowing investigators and regulatory agencies to compare MSCs used in different clinical trials.
引用
收藏
页码:32S / 35S
页数:4
相关论文
共 11 条
[1]   A reproducible immunopotency assay to measure mesenchymal stromal cell-mediated T-cell suppression [J].
Bloom, Debra D. ;
Centanni, John M. ;
Bhatia, Neehar ;
Emler, Carol A. ;
Drier, Diana ;
Leverson, Glen E. ;
Mckenna, David H., Jr. ;
Gee, Adrian P. ;
Lindblad, Robert ;
Hei, Derek J. ;
Hematti, Peiman .
CYTOTHERAPY, 2015, 17 (02) :140-151
[2]   Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[3]   The challenge of defining mesenchymal stromal cell potency assays and their potential use as release criteria [J].
Galipeau, Jacques ;
Krampera, Mauro .
CYTOTHERAPY, 2015, 17 (02) :125-127
[4]   Heterogeneity of mesenchymal stromal cell preparations [J].
Ho, A. D. ;
Wagner, W. ;
Franke, W. .
CYTOTHERAPY, 2008, 10 (04) :320-330
[5]   Mesenchymal Stromal Cells: New Directions [J].
Keating, Armand .
CELL STEM CELL, 2012, 10 (06) :709-716
[6]  
LAZARUS HM, 1995, BONE MARROW TRANSPL, V16, P557
[7]   Development of a surrogate angiogenic potency assay for clinical-grade stem cell production [J].
Lehman, Nicholas ;
Cutrone, Rochelle ;
Raber, Amy ;
Perry, Robert ;
Van't Hof, Wouter ;
Deans, Robert ;
Ting, Anthony E. ;
Woda, Juliana .
CYTOTHERAPY, 2012, 14 (08) :994-1004
[8]   Human bone marrow stromal cell confluence: effects on cell characteristics and methods of assessment [J].
Ren, Jiaqiang ;
Wang, Huan ;
Tran, Katherine ;
Civini, Sara ;
Jin, Ping ;
Castiello, Luciano ;
Feng, Ji ;
Kuznetsov, Sergei A. ;
Robey, Pamela G. ;
Sabatino, Marianna ;
Stroncek, David F. .
CYTOTHERAPY, 2015, 17 (07) :897-911
[9]  
Salmikangas P, 2015, REGEN MED, V10, P65, DOI [10.2217/rme.14.65, 10.2217/RME.14.65]
[10]   Mesenchymal stem or stromal cells: a review of clinical applications and manufacturing practices [J].
Sharma, Ratti Ram ;
Pollock, Kathryn ;
Hubel, Allison ;
McKenna, David .
TRANSFUSION, 2014, 54 (05) :1418-1437