Ignite Creation Date:
2024-05-05 @ 7:50 PM
Last Modification Date:
2024-10-26 @ 9:55 AM
Study NCT ID:
NCT00758992
Status:
COMPLETED
Last Update Posted:
2016-03-14
First Post:
2008-09-18
Brief Title:
Peripheral Blood Stem Cells Obtained From Normal Volunteers for Studying Retroviral Vector Mediated Gene Transfer Into Primitive Hematopoietic Cells and Vector Mediated Transgene Expression in Mature Hematopoietic Lineages
Sponsor:
St Jude Childrens Research Hospital
Organization:
St Jude Childrens Research Hospital
Study Overview
Official Title:
Peripheral Blood Stem Cells Obtained From Normal Volunteers for Studying Retroviral Vector Mediated Gene Transfer Into Primitive Hematopoietic Cells and Vector Mediated Transgene Expression in Mature Hematopoietic Lineages
Status:
COMPLETED
Status Verified Date:
2016-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
These studies are designed to evaluate the relative efficiency of gene transfer into primitive human hematopoietic cells by comparing lentiviral and foamy virus vectors as vehicles for transfer and expression of globin genes Normal volunteers will serve as research participants Each will receive a 4 day course of Granulocyte-Colony Stimulating Factor G-CSF after which a peripheral blood apheresis will be performed to recover a mononuclear cell population enriched in primitive hematopoietic cells The stem and progenitor cells will be purified by selection based on expression of the CD34 antigen The CD34 population will be cultured in vitro with various cytokines and transduced with vector particles The efficiency of gene transfer will be evaluated in the transduced CD34 population in progenitors contained within that population by culture in semisolid media and in cells capable of establishing human hematopoiesis in immunodeficient mice The level of transgene expression will be evaluated in mature hematopoietic lineages that develop in vitro or in immunodeficient mice
Detailed Description:
The peripheral blood has been established as a source of hematopoietic stem cells providing an alternative source to bone marrow for hematopoietic reconstitution of patients with oncologic hematologic and genetic diseases Although apheresis is less efficient than bone marrow harvesting for collection of large numbers of CD34 a marker of early hematopoietic precursors cells apheresis is less traumatic requires no anesthesia and can be performed more frequently than bone marrow harvesting The purpose of this preclinical research project is to investigate the use of hematopoietic stem cells mobilized into peripheral blood as targets for retroviral-mediated gene therapy to compare the efficiency of transduction of primitive cells with the lentiviral and foamy viral vector systems and to evaluate the ability to expand those stem cells ex vivo using hematopoietic growth factors cytokines Research participants in this study will be healthy adult volunteers
The growth factor Granulocyte-Colony Stimulating Factor G-CSF will be given for 4 days prior to apheresis to mobilize increased numbers of primitive hematopoietic cells from the bone marrow into the circulation Nucleated blood cells will be collected by apheresis and a CD34-enriched cell population isolated using antibody-based techniques
Administration of G-CSF is essential to allow collection of sufficient numbers of primitive stem and progenitor cells from normal volunteers In the dose to be used in this study a 15-35 fold increase in the concentration of CD34 cells occurs in peripheral blood over the 4 days of G-CSF administration resulting in an apheresis product which contains on average about 1-2 x1010 nucleated cells from which 1-2x108 purified CD34cells can be recovered This number is sufficient to allow an experimental design which includes in vitro culture transduction with vector particles and assay of transduced cells in the immunodeficient mouse model
The use of G-CSF for mobilization of stem and progenitor cells is a widely used clinical technique for both autologous and allogeneic transplantation which has proved both safe and effective Bone and muscle pain headache and fatigue are the most common complications which are typically managed with acetaminophen and rarely require discontinuation of G-CSF Transient elevations in alkaline phosphatase and LDH are common Follow-up studies have shown prolonged mild neutropenia lymphopenia and thrombocytopenia following G-CSF administration and apheresis Splenic enlargement has been shown by non-invasive measurements and four cases of splenic rupture in normal individuals have been described A reduction in arterial pO2 associated with a decrease in the O2 saturation from 98 to 96 has been reported Transient thrombophilia has been inferred based on changes in blood coagulation parameters
Other rare complications have been reported including the development of inflammatory or infectious lesions A fatal crisis occurred in a sibling donor for allogeneic transplantation who had hemoglobin SC disease These rare complications should be put in the context that G-CSF administration followed by apheresis to recover primitive hematopoietic cells from normal individuals has been utilized in all major transplant centers for more than a decade and has generally been safe and without significant complications We propose to minimize the risk of serious complications by limiting the age range of research participants to 18-40 years and excluding those with a history of inflammatory disease cardiovascular disease thrombosis or pulmonary embolization inflammatory skin disorders hematological disease or hemoglobinopathy
The ability to expand mobilized CD34 cells in vitro using various cytokine combinations and culture conditions will be examined using flow cytometry in vitro colony assays and by quantitating the concentration of cells that are able to establish hematopoiesis in immunodeficient mice Both unexpanded and expanded CD34 cells will be used in experiments designed to investigate their suitability as targets for retroviral-mediated gene transfer Gene transfer efficiency and functional expression of transferred sequences will be assessed in the differentiated progeny of CD34 cells
We plan to compare the lentiviral and foamy virus vector systems with respect to relative efficiency of gene transfer into primitive human hematopoietic cells Various substances eg Fibroblast Growth Factor -1 and Wnt 3A that have been reported to cause expansion of primitive murine hematopoietic cells will also be evaluated for their effects of primitive human hematopoietic cells in culture Another focus is the comparison of various globin gene vectors with respect to the relative levels of globin gene expression in differentiating erythroid cells Finally the impact of cryopreservation on viability and engraftment potential of primitive hematopoietic cells will be assessed This research proposal will provide preclinical data that will aid in the development of treatment strategies for genetic diseases specifically hemoglobin disorders based on gene transfer into repopulating stem cells
The growth factor Granulocyte-Colony Stimulating Factor G-CSF will be given for 4 days prior to apheresis to mobilize increased numbers of primitive hematopoietic cells from the bone marrow into the circulation Nucleated blood cells will be collected by apheresis and a CD34-enriched cell population isolated using antibody-based techniques
Administration of G-CSF is essential to allow collection of sufficient numbers of primitive stem and progenitor cells from normal volunteers In the dose to be used in this study a 15-35 fold increase in the concentration of CD34 cells occurs in peripheral blood over the 4 days of G-CSF administration resulting in an apheresis product which contains on average about 1-2 x1010 nucleated cells from which 1-2x108 purified CD34cells can be recovered This number is sufficient to allow an experimental design which includes in vitro culture transduction with vector particles and assay of transduced cells in the immunodeficient mouse model
The use of G-CSF for mobilization of stem and progenitor cells is a widely used clinical technique for both autologous and allogeneic transplantation which has proved both safe and effective Bone and muscle pain headache and fatigue are the most common complications which are typically managed with acetaminophen and rarely require discontinuation of G-CSF Transient elevations in alkaline phosphatase and LDH are common Follow-up studies have shown prolonged mild neutropenia lymphopenia and thrombocytopenia following G-CSF administration and apheresis Splenic enlargement has been shown by non-invasive measurements and four cases of splenic rupture in normal individuals have been described A reduction in arterial pO2 associated with a decrease in the O2 saturation from 98 to 96 has been reported Transient thrombophilia has been inferred based on changes in blood coagulation parameters
Other rare complications have been reported including the development of inflammatory or infectious lesions A fatal crisis occurred in a sibling donor for allogeneic transplantation who had hemoglobin SC disease These rare complications should be put in the context that G-CSF administration followed by apheresis to recover primitive hematopoietic cells from normal individuals has been utilized in all major transplant centers for more than a decade and has generally been safe and without significant complications We propose to minimize the risk of serious complications by limiting the age range of research participants to 18-40 years and excluding those with a history of inflammatory disease cardiovascular disease thrombosis or pulmonary embolization inflammatory skin disorders hematological disease or hemoglobinopathy
The ability to expand mobilized CD34 cells in vitro using various cytokine combinations and culture conditions will be examined using flow cytometry in vitro colony assays and by quantitating the concentration of cells that are able to establish hematopoiesis in immunodeficient mice Both unexpanded and expanded CD34 cells will be used in experiments designed to investigate their suitability as targets for retroviral-mediated gene transfer Gene transfer efficiency and functional expression of transferred sequences will be assessed in the differentiated progeny of CD34 cells
We plan to compare the lentiviral and foamy virus vector systems with respect to relative efficiency of gene transfer into primitive human hematopoietic cells Various substances eg Fibroblast Growth Factor -1 and Wnt 3A that have been reported to cause expansion of primitive murine hematopoietic cells will also be evaluated for their effects of primitive human hematopoietic cells in culture Another focus is the comparison of various globin gene vectors with respect to the relative levels of globin gene expression in differentiating erythroid cells Finally the impact of cryopreservation on viability and engraftment potential of primitive hematopoietic cells will be assessed This research proposal will provide preclinical data that will aid in the development of treatment strategies for genetic diseases specifically hemoglobin disorders based on gene transfer into repopulating stem cells
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| P01HL053749 | NIH | None | None |
| 2010037 | OTHER | Doris Duke Foundation | httpsreporternihgovquickSearchP01HL053749 |