Transduction of bone marrow cells by the AdZ.F(pK7) modified adenovirus demonstrates preferential gene transfer in myeloma cells.

Adenoviral vectors can efficiently infect myeloma cell lines, but transduction of fresh myeloma cells performed at low multiplicity of infections (MOIs) showed only partial efficacy. The modified adenoviral vector AdZ.F(pK7), through binding of polylysines to heparan sulfate-containing receptors, could increase virus adsorption and gene transfer efficiency in myeloma cells, which express heparan sulfate-containing receptors. Thus, we investigated the ability of AdZ.F(pK7) vector to achieve efficient gene transfer in primary cultured fresh myeloma cells. Transduction of 16 primary cultured myeloma samples showed that gene transfer was much more efficient with AdZ.F(pK7) than with control AdZ.F. Both addition of soluble heparin and cell treatment with heparinase I dramatically inhibited gene transfer in myeloma cells by AdZ.F(pK7) but had no effect with AdZ.F, while addition of recombinant fiber protein inhibited AdZ.F but not AdZ.F(pK7), confirming that AdZ.F(pK7) gene transfer in myeloma cells is mediated by the targeting of heparan sulfates. AdZ.F(pK7) transduction of bone marrow cells showed that myeloma cells and hematopoietic progenitor AC133-, CD34-, and CD33-positive cells were efficiently transduced at an MOI of 100, but that only myeloma cells were significantly transduced at an MOI of 12. Thus, AdZ.F(pK7) vector seems to be well suited for immunological approaches of gene therapy or bone marrow-purging applications in multiple myeloma.

[1]  M. Dewhirst,et al.  Enhancement of radiotherapy by hyperthermia-regulated gene therapy. , 2000, International journal of radiation oncology, biology, physics.

[2]  B. Quesnel,et al.  Increased gene transfer in acute myeloid leukemic cells by an adenovirus vector containing a modified fiber protein , 1999, Gene Therapy.

[3]  K. Anderson,et al.  Adenovirus vector-based purging of multiple myeloma cells. , 1998, Blood.

[4]  B. Lord,et al.  CD34+AC133+ Cells Isolated from Cord Blood are Highly Enriched in Long‐Term Culture‐Initiating Cells, NOD/SCID‐Repopulating Cells and Dendritic Cell Progenitors , 1998, Stem cells.

[5]  G. Dranoff,et al.  Cancer gene therapy: connecting basic research with clinical inquiry. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[6]  W. Dalton,et al.  Broadened clinical utility of gene gun-mediated, granulocyte-macrophage colony-stimulating factor cDNA-based tumor cell vaccines as demonstrated with a mouse myeloma model. , 1998, Human gene therapy.

[7]  B. Barlogie,et al.  Syndecan-1 is a multifunctional regulator of myeloma pathobiology: control of tumor cell survival, growth, and bone cell differentiation. , 1998, Blood.

[8]  S. Shammah,et al.  Adenovirus vectors for gene transduction into mobilized blood CD34+ cells , 1998, Gene Therapy.

[9]  F. Graham,et al.  In vivo adenoviral-mediated gene transfer of interleukin-2 in cutaneous plasmacytoma. , 1998, Blood.

[10]  J. Bergelson,et al.  The Murine CAR Homolog Is a Receptor for Coxsackie B Viruses and Adenoviruses , 1998, Journal of Virology.

[11]  F. Paillard Immuno-Gene Therapy for Myeloma Using Cytokines Suicide Genes Against Brain Tumors , 1998 .

[12]  S. Rudikoff,et al.  Interleukin-2-mediated modulation of plasma cell tumor growth in a model of multiple myeloma. , 1998, Human gene therapy.

[13]  S. Gallinger,et al.  Efficient adenovirus-mediated gene expression in malignant human plasma cells: relative lymphoid cell resistance. , 1998, Experimental hematology.

[14]  J. Kearney,et al.  AC133, a novel marker for human hematopoietic stem and progenitor cells. , 1997, Blood.

[15]  R. Warnke,et al.  A novel five-transmembrane hematopoietic stem cell antigen: isolation, characterization, and molecular cloning. , 1997, Blood.

[16]  D. Brough,et al.  Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins , 1997, Journal of virology.

[17]  B. Trapnell,et al.  Evaluation of the concentration and bioactivity of adenovirus vectors for gene therapy , 1996, Journal of virology.

[18]  D. Brough,et al.  Adenovirus targeted to heparan-containing receptors increases its gene delivery efficiency to multiple cell types , 1996, Nature Biotechnology.

[19]  H. Haddada,et al.  Differential efficacy of adenoviral mediated gene transfer into cells from hematological cell lines and fresh hematological malignancies. , 1996, Leukemia.

[20]  J. Woodliff,et al.  Expression of syndecan regulates human myeloma plasma cell adhesion to type I collagen , 1993 .