Transfusion and Apheresis Science
Volume 30, Issue 1 , Pages 47-54, February 2004

Effect of cryopreservation on the immunogenicity of umbilical cord blood cells

  • Natkunam Ketheesan

      Affiliations

    • Microbiology and Immunology, James Cook University, Queensland, Australia 4811
    • School of Medicine, James Cook University, Queensland, Australia 4811
    • Corresponding Author InformationCorresponding author. Tel.: +61-7-4781-6876; fax: +61-7-4779-1526
  • ,
  • Cass Whiteman

      Affiliations

    • Microbiology and Immunology, James Cook University, Queensland, Australia 4811
    • School of Medicine, James Cook University, Queensland, Australia 4811
  • ,
  • Agnieszka B. Malczewski

      Affiliations

    • School of Medicine, James Cook University, Queensland, Australia 4811
  • ,
  • Robert G. Hirst

      Affiliations

    • Microbiology and Immunology, James Cook University, Queensland, Australia 4811
  • ,
  • Justin T. La Brooy

      Affiliations

    • School of Medicine, James Cook University, Queensland, Australia 4811

Received in revised form 1 January 2003; accepted 1 May 2003.

Abstract 

Cryopreservation is the accepted method for long-term storage of cord blood (CB) cells. We evaluated the effects of using different cooling rates (1, 5, 7.5 and 10 °C/min) on CB cell allostimulatory and alloproliferative function, antigen expression and clonogenic potential. Significant decreases (P<0.001–0.003) in viable cell recovery observed between fresh CB cells and CB cells cryopreserved at each cooling rate tested. Reductions in clonogenic potential of CB cells cryopreserved at cooling rates of 1, 5, 7.5 and 10 °C/min were 44%, 76%, 88% and 93% respectively, compared to fresh controls. FACS analysis indicated no changes in percentages CD34+ cells or lymphocytes. Two sets of mixed lymphocyte reactions were carried out for each CB sample. It was observed that allostimulatory and alloproliferative function varied following cryopreservation at different cooling rates (1 and 5 °C/min). Interestingly, there was a significant decrease (P<0.001–0.04) in the alloproliferative function of six of the seven CB samples following cryopreservation using a cooling rate of 5 °C/min. Cooling rates between 1 and 5 °C/min may provide immunomodulation of CB with maintenance of haematopoietic progenitor cells function.

Keywords:  Cord blood, Umbilical cord blood, Cryopreservation, Immunomodulation, Mixed lymphocyte reaction

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PII: S1473-0502(03)00195-2

doi:10.1016/j.transci.2003.05.002

Transfusion and Apheresis Science
Volume 30, Issue 1 , Pages 47-54, February 2004