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Research Article

CD34+ cell selection using small-volume marrow aspirates: a platform for novel cell therapies and regenerative medicine

, , , , , , , , , , , , & show all
Pages 170-177 | Received 13 Aug 2009, Accepted 10 Nov 2009, Published online: 18 Jan 2010
 

Abstract

Background aims. This study was initiated to determine whether CD34+ cell selection of small-volume bone marrow (BM) samples could be performed effectively on the Isolex® 300i Magnetic Cell Selection System® device and whether the results obtained from these samples were comparable with results from large standard-volume samples. The impact on CD34+ recovery using a full versus half vial of Isolex® CD34 reagent and the effects of shipping a post-selection product were evaluated. Methods. A protocol to evaluate CD34+ cell selection with two ranges of smaller volume BM samples (c. 50 mL and c. 100 mL) was developed and instituted at three Production Assistance for Cellular Therapies (PACT) facilities. The study was performed in two phases. Results. In phase I, the mean post-selection CD34+ recoveries from the two sizes of samples were 104.1% and 103.3% (smallest and largest volumes, respectively), and mean CD34+ recoveries were 115.6% and 88.7%, with full and half vials of reagent, respectively. Mean CD34+ recoveries for post-shipment smaller volume samples were 106.8% and for larger volume samples 116.4%; mean CD34+ recoveries were 99.9% and 127.4% for post-shipment samples processed with full and half vials of reagent, respectively. In phase II, mean CD34+ recovery was 76.8% for post-selection samples and 74.0% for post-shipment samples. Conclusions. The results suggest that smaller volume BM sample processing on the Isolex® system is as efficient or more efficient compared with standard-volume sample processing. Post-processing mean CD34+ recovery results obtained using a full or half vial of CD34 reagent were not significantly different.

Acknowledgments

This work was supported in part by PACT (NHLBI contract numbers N01-HB-37163, N01-HB-37164, N01-HB-37165 and N01-HB-37166.) The authors would like to thank the staff at Baylor College of Medicine, University of Minnesota and University of Pittsburgh for sample collection and testing. In addition, we would like to thank Baxter Healthcare Corporation for providing the Isolex® reagents and the EMMES Corporation for advice on the statistical analysis of the data.

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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