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2006 | 53 | 4 | 815-823

Article title

Optimization of a retroviral vector for transduction of human CD34 positive cells

Content

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EN

Abstracts

EN
Human stem and progenitor cells have recently become objects of intensive studies as an important target for gene therapy and regenerative medicine. Retroviral vectors are among the most effective tools for genetic modification of these cells. However, their transduction efficiency strongly depends on the choice of the ex vivo transduction system. The aim of this study was to elaborate a system for retroviral vector transduction of human CD34 positive cells isolated from cord blood. The retroviral vector pMINV EGFP was chosen for transduction of two human erythroblastoid cell lines: KG-1a (CD34 positive) and K562 (CD34 negative). For vector construction, three promoters and two retroviral vector packaging cell lines were used. To optimize the physicochemical conditions of the transduction process, different temperatures of supernatant harvesting, the influence of centrifugation and the presence of transduction enhancing agents were tested. The conditions elaborated with KG-1a cells were further applied for transduction of CD34 positive cells isolated from cord blood. The optimal efficiency of transduction of CD34 positive cells with pMINV EGFP retroviral vector (26% of EGFP positive cells), was obtained using infective vector with LTR retroviral promoter, produced by TE FLY GA MINV EGFP packaging cell line. The transduction was performed in the presence of serum, at 37°C, with co-centrifugation of cells with viral supernatants and the use of transduction enhancing agents. This study confirmed that for gene transfer into CD34 positive cells, the detailed optimization of each element of the transduction process is of great importance.

Year

Volume

53

Issue

4

Pages

815-823

Physical description

Dates

published
2006
received
2006-07-03
revised
2006-10-31
accepted
2006-12-07
(unknown)
2006-12-11

Contributors

author
  • Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland
  • Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland
  • Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland
  • Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland
  • Chair of Obstetrics and Gynecology of Wrocław Medical University, Wrocław, Poland
  • Department of Cancer Immunology, Chair of Oncology, University of Medical Sciences at Great Poland Cancer Center, Poznań, Poland
  • Department of Cancer Immunology, Chair of Oncology, University of Medical Sciences at Great Poland Cancer Center, Poznań, Poland
author
  • Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland

References

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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv53p815kz
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