Session Information
AABB Audioconference Series 2013
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HCT Product Quality and Viability Assessment for the CT Laboratory
Track : Cellular Therapy
Program Code: 134763
Date: Wednesday, October 23, 2013
Time: 2:00 PM to 3:30 PM  EST
DIRECTOR :
M. Vic Lemas, PhD, Lab Director, Cell Therapy Laboratory, Johns Hopkins Medicine
SPEAKER :
Michael Creer, MD, Director, Clinical Laboratories and Chief, Clinical Pathology, Penn State Hershey Medical Center
HCT Product Quality and Viability Assessment for the CT Laboratory
Description
Engraftment following transplantation of an HCT product is critically dependent upon infusion of a sufficient number (dose) of viable, functional hematopoietic stem/progenitor cells (HPC). Accordingly, although the total nucleated cell (TNC) and CD34+ cell content are the primary features that are used to determine whether an HCT product is suitable for transplantation, it is also vitally important to evaluate HPC viability and function. This is especially true when HCT processing is delayed, the HCT product is manipulated, the HCT product requires shipment over large geographic distances and/or the HCT product is cryopreserved. This session will provide a focused discussion of commonly used methods to assess TNC and HPC cell viability with specific emphasis placed on improving the general understanding of how different methods work, the advantages and limitations of different approaches, the practical details of implementing these methods in the cell therapy laboratory and the unique challenges encountered with attempts to standardize these techniques.

*CT Program

You will have the ability to purchase CD-ROMs of this Audioconference 2 weeks after the session has been presented. For any questions, please contact MultiviewMediaSupport@multiview.com.

LEARNER OUTCOMES:
  • Describe approaches that permit the use of flow cytometry to specifically evaluate the viability of the granulocyte, monocyte and lymphocyte populations separately using 7-AAD during the same analysis of CD34+ cell viability and effects of time and temperature on dye-based cell viability assessment.
  • Discuss factors influencing the results obtained by these methods and how results differ when measured before cryopreservation and after thaw.
  • Discuss the original ISHAGE method for CD34+ cell quantitation and recent modifications of the original method to include the use of fluorescent beads for single-platform cell counting and inclusion of 7-AAD to assess CD34+ cell viability.
  • Discuss the results of external proficiency testing programs to evaluate the performance of different laboratories in the determination of cell viability and discuss the challenges to the standardization of cell viability assessment and measurement of "viable" CD34+ cell count.
  • Discuss the use of trypan blue, acridine orange/propidium iodide (AO/PI) and other similar techniques to assess total nucleated cell (TNC) viability based on "dye exclusion" by viable cells.


CE CategoryCE Value
California Clinical Laboratory Personnel 1.5
California Nurse 1.8
Florida Laboratory Personnel 1.8
General Attendee 1.5
Physician 1.5
Please note: Continuing education (CE) credit is available for online offerings only. Individuals that purchase CD-ROMs will not receive CE credit for the programs they view.


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