Shipping of Therapeutic Somatic Cell Products
02/2011
Journal Article
Authors:
Whiteside, T.;
Griffin, D.;
Stanson, J.;
Gooding, W.;
McKenna, D.;
Sumstad, D.;
Kadidlo, D.;
Gee, A.;
Durett, A.;
Lindblad, R.;
Wood, D.;
Styers, D.
Secondary:
Cytotherapy
Volume:
13
Pagination:
201-213
URL:
http://www.ncbi.nlm.nih.gov/pubmed/20795760
Keywords:
Cell products for therapy; somatic cell products; transport of somatic cells; validation of cell shipping
Abstract:
Background aims. Shipment of therapeutic somatic cells between a current good manufacturing practice (cGMP) facility and a clinic or between different cGMP facilities requires validated standard operating procedures (SOP). Under National Heart Lung & Blood Institute (NHLBI) sponsorship, the Production Assistance for Cellular Therapies (PACT) group conducted a validation study for the shipping SOP it has created, including shipments of cryopreserved somatic cells, fresh peripheral blood specimens and apheresis products. Methods. Comparisons of pre- and post-shipped cells and cell products at the three participating facilities included measurements of viability, phenotypic profiles and cellular functions. The data were analyzed at the University of Pittsburgh Biostatistics Facility. Results. No consistent shipping effects on cell viability, phenotype or functions were detected for cryopreserved and shipped peripheral blood mononuclear cells (PBMC), monocytes, immature dendritic cells (iDC), NK-92 or cytotoxic T cells (CTL). Cryopreserved mesenchymal stromal cells (MSC) had a significantly decreased viability after shipment, but this effect was in part because of inter-laboratory variability in the viable cell counts. Shipments of fresh peripheral blood and apheresis products for the generation of CTL and dendritic cells (DC), respectively, had no significant effects on cell product quality. MSC were successfully generated from fresh bone marrow samples shipped overnight. Conclusions. This validation study provides a useful set of data for guiding shipments of therapeutic somatic cells in multi-institutional clinical trials.
