Substantial Improvements in Performance Indicators Achieved in a Peripheral Blood Mononuclear Cell Cryopreservation Quality Assurance Program Using Single Donor Samples
- 1 January 2007
- journal article
- Published by American Society for Microbiology in Clinical and Vaccine Immunology
- Vol. 14 (1) , 52-59
- https://doi.org/10.1128/cvi.00214-06
Abstract
Storage of high-quality cryopreserved peripheral blood mononuclear cells (PBMC) is often a requirement for multicenter clinical trials and requires a reproducibly high standard of practice. A quality assurance program (QAP) was established to assess an Australia-wide network of laboratories in the provision of high-quality PBMC (determined by yield, viability, and function), using blood taken from single donors (human immunodeficiency virus [HIV] positive and HIV negative) and shipped to each site for preparation and cryopreservation of PBMC. The aim of the QAP was to provide laboratory accreditation for participation in clinical trials and cohort studies which require preparation and cryopreservation of PBMC and to assist all laboratories to prepare PBMC with a viability of >80% and yield of >50% following thawing. Many laboratories failed to reach this standard on the initial QAP round. Interventions to improve performance included telephone interviews with the staff at each laboratory, two annual wet workshops, and direct access to a senior scientist to discuss performance following each QAP round. Performance improved substantially in the majority of sites that initially failed the QAP ( P = 0.002 and P = 0.001 for viability and yield, respectively). In a minority of laboratories, there was no improvement ( n = 2), while a high standard was retained at the laboratories that commenced with adequate performance ( n = 3). These findings demonstrate that simple interventions and monitoring of PBMC preparation and cryopreservation from multiple laboratories can significantly improve performance and contribute to maintenance of a network of laboratories accredited for quality PBMC fractionation and cryopreservation.Keywords
This publication has 14 references indexed in Scilit:
- Maximizing the retention of antigen specific lymphocyte function after cryopreservationJournal of Immunological Methods, 2005
- Enhancing the Sensitivity of Assays to Detect T Cell Reactivity: The Effect of Cell Separation and Cryopreservation MediaAnnals of the New York Academy of Sciences, 2004
- CD4+ and CD8+ cells in cryopreserved human PBMC maintain full functionality in cytokine ELISPOT assaysJournal of Immunological Methods, 2003
- Correlates of Antiviral Immune Restoration in Acute and Chronic HIV Type 1 Infection: Sustained Viral Suppression and Normalization of T Cell SubsetsAIDS Research and Human Retroviruses, 2002
- A panel of MHC class I restricted viral peptides for use as a quality control for vaccine trial ELISPOT assaysJournal of Immunological Methods, 2002
- Monitoring HIV-specific CD8+ T cell responses by intracellular cytokine productionImmunology Letters, 2001
- Development and Validation of a Gamma Interferon ELISPOT Assay for Quantitation of Cellular Immune Responses to Varicella-Zoster VirusClinical and Diagnostic Laboratory Immunology, 2001
- Apoptosis-Related Mortality in Vitro of Mononuclear Cells from Patients with HIV Infection Correlates with Disease Severity and ProgressionJAIDS Journal of Acquired Immune Deficiency Syndromes, 1995
- Viro-immunological studies in acute HIV-1 infectionAIDS, 1994
- Analysis of serial measurements in medical research.BMJ, 1990