TY - JOUR
T1 - Nomenclature and heterogeneity
T2 - consequences for the use of mesenchymal stem cells in regenerative medicine
AU - Wilson, Alison Jane
AU - Webster, Andrew Joseph
AU - Genever, Paul Gilbert
N1 - © 2019 AJ Wilson, AJ Webster, PG Genever
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Mesenchymal stem cells (MSCs) are in development for many clinical indications, based both on “stem” properties (tissue repair or regeneration) and on signalling repertoire (immunomodulatory and anti-inflammatory effects). Potential conflation of MSC properties with those of tissue-derived stromal cells presents difficulties in comparing study outcomes and represents a source of confusion in cell therapy development. Cultured MSCs demonstrate significant heterogeneity in clonogenicity and multi-lineage differentiation potential. However in vivo biology of MSCs includes native functions unrelated to regenerative medicine applications, so do nomenclature and heterogeneity matter? In this perspective we examine some consequences of the nomenclature debate and heterogeneity of MSCs. Regulatory expectations are considered, emphasising that product development should prioritise detailed characterisation of therapeutic cell populations for specific indications.
AB - Mesenchymal stem cells (MSCs) are in development for many clinical indications, based both on “stem” properties (tissue repair or regeneration) and on signalling repertoire (immunomodulatory and anti-inflammatory effects). Potential conflation of MSC properties with those of tissue-derived stromal cells presents difficulties in comparing study outcomes and represents a source of confusion in cell therapy development. Cultured MSCs demonstrate significant heterogeneity in clonogenicity and multi-lineage differentiation potential. However in vivo biology of MSCs includes native functions unrelated to regenerative medicine applications, so do nomenclature and heterogeneity matter? In this perspective we examine some consequences of the nomenclature debate and heterogeneity of MSCs. Regulatory expectations are considered, emphasising that product development should prioritise detailed characterisation of therapeutic cell populations for specific indications.
U2 - 10.2217/rme-2018-0145
DO - 10.2217/rme-2018-0145
M3 - Article
SN - 1746-0751
VL - 14
SP - 595
EP - 611
JO - REGENERATIVE MEDICINE
JF - REGENERATIVE MEDICINE
IS - 6
ER -