The presence of an autologous marrow stromal cell layer increases glucocerebrosidase gene transduction of long-term culture initiating cells (LTCICs) from the bone marrow of a patient with Gaucher disease

S. Wells, P. Malik, M. Pensiero, D. B. Kohn, Jan Nolta

Research output: Contribution to journalArticle

39 Citations (Scopus)

Abstract

Gaucher disease is a lysosomal storage disorder resulting from deficiency of the acid β-glucosidase, glucocerebrosidase (GC). Allogeneic bone marrow transplantation has been beneficial in the treatment of Gaucher patients. Therefore, this disorder may be an ideal candidate for gene therapy by GC gene transduction of hematopoietic stem cells. We sought to increase the extent of gene transfer into CD34+ cells from the marrow of a Gaucher patient using G1GC, a simple retroviral vector containing a normal human GC cDNA. The ability of autologous stromal support and recombinant cytokines to increase the extent of transduction of colony-forming cells (CFCs) and long-term culture initiating cells (LTCICs) was assessed. The presence of a stromal layer significantly increased the extent of GC gene transfer into 14-day CFCs, as determined bypoiymerase chain reaction (PCR) of individual colonies (18.8% with stroma versus 5% without, P < 0.001), Stromal support also increased the extent of transduction of L TCICs (10% with stroma versus 0.83% without, P < 0.001). Non-adherent cells from long-term bone marrow cultures initiated with CD34+ progenitors transduced on autologous stroma had higher levels of GC enzyme activity than cultures initiated with cells transduced without stroma. The percentage of cells which were GC positive by immunohistochemistry was also increased (21.1% with stroma versus 2.7% without, P = 0.0003). The addition ofcytokines (IL-3, IL-6 and Steel factor) to the transduction, in the presence of stroma, significantly increased the extent of gene transfer into CFCs but not LTCICs. These studies Indicate that the GC gene can be effectively transduced into LTCICs by retroviral vectors in the presence of stroma at levels significant for clinical gene therapy trials in patients with Gaucher disease.

Original languageEnglish (US)
Pages (from-to)512-520
Number of pages9
JournalGene Therapy
Volume2
Issue number8
StatePublished - 1995
Externally publishedYes

Fingerprint

Glucosylceramidase
Gaucher Disease
Stromal Cells
Bone Marrow Cells
Bone Marrow
Genes
Cell Culture Techniques
Genetic Therapy
Glucosidases
Stem Cell Factor
Interleukin-3
Homologous Transplantation
Hematopoietic Stem Cells
Bone Marrow Transplantation
Interleukin-6
Complementary DNA
Immunohistochemistry
Cytokines
Polymerase Chain Reaction
Acids

Keywords

  • Gaucher disease
  • Gene therapy
  • Hematopoietic progenitor cells
  • Retroviral vector
  • Stromal cells

ASJC Scopus subject areas

  • Genetics

Cite this

@article{a96dc3d314974c8d9edbf18017117ae2,
title = "The presence of an autologous marrow stromal cell layer increases glucocerebrosidase gene transduction of long-term culture initiating cells (LTCICs) from the bone marrow of a patient with Gaucher disease",
abstract = "Gaucher disease is a lysosomal storage disorder resulting from deficiency of the acid β-glucosidase, glucocerebrosidase (GC). Allogeneic bone marrow transplantation has been beneficial in the treatment of Gaucher patients. Therefore, this disorder may be an ideal candidate for gene therapy by GC gene transduction of hematopoietic stem cells. We sought to increase the extent of gene transfer into CD34+ cells from the marrow of a Gaucher patient using G1GC, a simple retroviral vector containing a normal human GC cDNA. The ability of autologous stromal support and recombinant cytokines to increase the extent of transduction of colony-forming cells (CFCs) and long-term culture initiating cells (LTCICs) was assessed. The presence of a stromal layer significantly increased the extent of GC gene transfer into 14-day CFCs, as determined bypoiymerase chain reaction (PCR) of individual colonies (18.8{\%} with stroma versus 5{\%} without, P < 0.001), Stromal support also increased the extent of transduction of L TCICs (10{\%} with stroma versus 0.83{\%} without, P < 0.001). Non-adherent cells from long-term bone marrow cultures initiated with CD34+ progenitors transduced on autologous stroma had higher levels of GC enzyme activity than cultures initiated with cells transduced without stroma. The percentage of cells which were GC positive by immunohistochemistry was also increased (21.1{\%} with stroma versus 2.7{\%} without, P = 0.0003). The addition ofcytokines (IL-3, IL-6 and Steel factor) to the transduction, in the presence of stroma, significantly increased the extent of gene transfer into CFCs but not LTCICs. These studies Indicate that the GC gene can be effectively transduced into LTCICs by retroviral vectors in the presence of stroma at levels significant for clinical gene therapy trials in patients with Gaucher disease.",
keywords = "Gaucher disease, Gene therapy, Hematopoietic progenitor cells, Retroviral vector, Stromal cells",
author = "S. Wells and P. Malik and M. Pensiero and Kohn, {D. B.} and Jan Nolta",
year = "1995",
language = "English (US)",
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journal = "Gene Therapy",
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T1 - The presence of an autologous marrow stromal cell layer increases glucocerebrosidase gene transduction of long-term culture initiating cells (LTCICs) from the bone marrow of a patient with Gaucher disease

AU - Wells, S.

AU - Malik, P.

AU - Pensiero, M.

AU - Kohn, D. B.

AU - Nolta, Jan

PY - 1995

Y1 - 1995

N2 - Gaucher disease is a lysosomal storage disorder resulting from deficiency of the acid β-glucosidase, glucocerebrosidase (GC). Allogeneic bone marrow transplantation has been beneficial in the treatment of Gaucher patients. Therefore, this disorder may be an ideal candidate for gene therapy by GC gene transduction of hematopoietic stem cells. We sought to increase the extent of gene transfer into CD34+ cells from the marrow of a Gaucher patient using G1GC, a simple retroviral vector containing a normal human GC cDNA. The ability of autologous stromal support and recombinant cytokines to increase the extent of transduction of colony-forming cells (CFCs) and long-term culture initiating cells (LTCICs) was assessed. The presence of a stromal layer significantly increased the extent of GC gene transfer into 14-day CFCs, as determined bypoiymerase chain reaction (PCR) of individual colonies (18.8% with stroma versus 5% without, P < 0.001), Stromal support also increased the extent of transduction of L TCICs (10% with stroma versus 0.83% without, P < 0.001). Non-adherent cells from long-term bone marrow cultures initiated with CD34+ progenitors transduced on autologous stroma had higher levels of GC enzyme activity than cultures initiated with cells transduced without stroma. The percentage of cells which were GC positive by immunohistochemistry was also increased (21.1% with stroma versus 2.7% without, P = 0.0003). The addition ofcytokines (IL-3, IL-6 and Steel factor) to the transduction, in the presence of stroma, significantly increased the extent of gene transfer into CFCs but not LTCICs. These studies Indicate that the GC gene can be effectively transduced into LTCICs by retroviral vectors in the presence of stroma at levels significant for clinical gene therapy trials in patients with Gaucher disease.

AB - Gaucher disease is a lysosomal storage disorder resulting from deficiency of the acid β-glucosidase, glucocerebrosidase (GC). Allogeneic bone marrow transplantation has been beneficial in the treatment of Gaucher patients. Therefore, this disorder may be an ideal candidate for gene therapy by GC gene transduction of hematopoietic stem cells. We sought to increase the extent of gene transfer into CD34+ cells from the marrow of a Gaucher patient using G1GC, a simple retroviral vector containing a normal human GC cDNA. The ability of autologous stromal support and recombinant cytokines to increase the extent of transduction of colony-forming cells (CFCs) and long-term culture initiating cells (LTCICs) was assessed. The presence of a stromal layer significantly increased the extent of GC gene transfer into 14-day CFCs, as determined bypoiymerase chain reaction (PCR) of individual colonies (18.8% with stroma versus 5% without, P < 0.001), Stromal support also increased the extent of transduction of L TCICs (10% with stroma versus 0.83% without, P < 0.001). Non-adherent cells from long-term bone marrow cultures initiated with CD34+ progenitors transduced on autologous stroma had higher levels of GC enzyme activity than cultures initiated with cells transduced without stroma. The percentage of cells which were GC positive by immunohistochemistry was also increased (21.1% with stroma versus 2.7% without, P = 0.0003). The addition ofcytokines (IL-3, IL-6 and Steel factor) to the transduction, in the presence of stroma, significantly increased the extent of gene transfer into CFCs but not LTCICs. These studies Indicate that the GC gene can be effectively transduced into LTCICs by retroviral vectors in the presence of stroma at levels significant for clinical gene therapy trials in patients with Gaucher disease.

KW - Gaucher disease

KW - Gene therapy

KW - Hematopoietic progenitor cells

KW - Retroviral vector

KW - Stromal cells

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