Literature DB >> 11033026

Apoptosis: a method for evaluating the cryopreservation of whole blood and peripheral blood mononuclear cells.

K R Fowke1, J Behnke, C Hanson, K Shea, L M Cosentino.   

Abstract

We sought to compare the effect of cryopreservation and storage at -30 degrees C, -70 degrees C and -150 degrees C of human whole blood versus matched peripheral blood mononuclear cell (PBMC) samples using apoptosis as an indicator of cell fitness. Following 10 weeks of storage the samples were thawed and assessed for viability (trypan blue exclusion), levels of apoptosis (using the nuclear stain bis-benzimide) and cell function (ability to be transformed by Epstein-Barr virus, EBV). When comparing storage temperatures, the levels of apoptosis in whole blood and PBMC samples stored at -30 degrees C were significantly higher than the values for samples stored at -70 degrees C or -150 degrees C (P<0.004). Whole blood samples stored at -150 degrees C had significantly less apoptosis than those stored at -70 degrees C (P<0.03). A comparison of the cell preparations showed that at all three storage temperatures there was significant sample deterioration (viability, apoptosis, and function) in whole blood relative to PBMC samples. This study indicates that careful consideration should be given to storage conditions and that apoptosis can be used as a sensitive measure of cell fitness following cryopreservation.

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Year:  2000        PMID: 11033026     DOI: 10.1016/s0022-1759(00)00263-5

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  14 in total

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2.  Cryopreservation: An emerging paradigm change.

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4.  Viable mononuclear cell stability study for implementation in a proficiency testing program: impact of shipment conditions.

Authors:  Olga A Kofanova; Kristine Davis; Barbara Glazer; Yvonne De Souza; Joseph Kessler; Fotini Betsou
Journal:  Biopreserv Biobank       Date:  2014-06       Impact factor: 2.300

5.  Comparison of peripheral blood mononuclear cell isolation techniques and the impact of cryopreservation on human lymphocytes expressing CD39 and CD73.

Authors:  Ross J Turner; Nicholas J Geraghty; Jonathan G Williams; Diane Ly; Daniel Brungs; Martin G Carolan; Thomas V Guy; Debbie Watson; Jeremiah F de Leon; Ronald Sluyter
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6.  Toward Optimal Cryopreservation and Storage for Achievement of High Cell Recovery and Maintenance of Cell Viability and T Cell Functionality.

Authors:  Stephanie Angel; Hagen von Briesen; Young-Joo Oh; Marko K Baller; Heiko Zimmermann; Anja Germann
Journal:  Biopreserv Biobank       Date:  2016-10-28       Impact factor: 2.300

7.  Substantial improvements in performance indicators achieved in a peripheral blood mononuclear cell cryopreservation quality assurance program using single donor samples.

Authors:  Wayne B Dyer; Sarah L Pett; John S Sullivan; Sean Emery; David A Cooper; Anthony D Kelleher; Andrew Lloyd; Sharon R Lewin
Journal:  Clin Vaccine Immunol       Date:  2006-10-18

8.  Loss of T cell responses following long-term cryopreservation.

Authors:  Rachel E Owen; Elizabeth Sinclair; Brinda Emu; John W Heitman; Dale F Hirschkorn; C Lorrie Epling; Qi Xuan Tan; Brian Custer; Jeffery M Harris; Mark A Jacobson; Joseph M McCune; Jeffery N Martin; Frederick M Hecht; Steven G Deeks; Philip J Norris
Journal:  J Immunol Methods       Date:  2007-08-08       Impact factor: 2.303

9.  Freezing Responses in DMSO-Based Cryopreservation of Human iPS Cells: Aggregates Versus Single Cells.

Authors:  Rui Li; Guanglin Yu; Samira M Azarin; Allison Hubel
Journal:  Tissue Eng Part C Methods       Date:  2018-03-28       Impact factor: 3.056

10.  Complementary role of HCV and HIV in T-cell activation and exhaustion in HIV/HCV coinfection.

Authors:  Thijs Feuth; Joop E Arends; Justin H Fransen; Nening M Nanlohy; Karel J van Erpecum; Peter D Siersema; Andy I M Hoepelman; Debbie van Baarle
Journal:  PLoS One       Date:  2013-03-15       Impact factor: 3.240

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