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Cryopreservation does not alter main characteristics of Good Manufacturing Process--grade human multipotent mesenchymal stromal cells including immunomodulating potential and lack of malignant transformation.

Authors :
LUETZKENDORF, JANA
NERGER, KATRIN
HERING, JULIAN
MOEGEL, ANGELIKA
HOFFMANN, KATRIN
HOEFERS, CHRISTIANE
MUELLER-TIDOW, CARSTEN
MUELLER, LUTZ P.
Source :
Cytotherapy (Elsevier Inc.). Feb2015, Vol. 17 Issue 2, p186-198. 13p.
Publication Year :
2015

Abstract

Background aims. The immunomodulating capacity of multipotent mesenchymal stromal cells (MSCs) qualifies them as a therapeutic tool in several diseases. However, repeated transplantation with products of reproducible characteristics may be required. This could be achieved with cryopreserved aliquots of Good Manufacturing Practice (GMP)-grade MSCs. However, the impact of cryopreservation on the characteristics of GMP-MSCs is ill defined. Methods. We produced fresh and cryopreserved MSCs from human donors with a xenogen-free GMP protocol. Immunogenicity and immunomodulating capacity were tested in co-culture with putative recipient-specific peripheral blood mononuclear cells (PBMCs). Risk of malignant transformation was assessed in vitro and in vivo. Results. Cryopreservation had no impact on viability and consensus criteria of MSCs. In co-culture with PBMCs, MSCs showed low immunogenicity and suppressed mitogenstimulated proliferation of PBMC irrespective of cryopreservation. Cytogenetic aberrations were not observed consistently in fresh and cryopreserved products, and no signs of malignant transformation occurred in functional assays. MSC products from an elderly pretreated donor showed reduced functional quality, but imminent failure of functional criteria could be detected by an increased population doubling time in early passages. Discussion. This study is the first systematic analysis on cryopreservation of xenogen-free human bone marrow--derived GMP-MSCs. The data support that cryopreservation does not alter the characteristics of the cells and thus may allow the generation of products for serial transplantation. In addition, the protocol allowed early detection of MSC products with low functional capacity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14653249
Volume :
17
Issue :
2
Database :
Academic Search Index
Journal :
Cytotherapy (Elsevier Inc.)
Publication Type :
Academic Journal
Accession number :
101117976
Full Text :
https://doi.org/10.1016/j.jcyt.2014.10.018