ImmunodeficiencyNCT00758992
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
An observational study of Immunodeficiency, run by St. Jude Children's Research Hospital at 1 site in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 40 yearsHealthy volunteers can take part
- Conditions the study is for
- Immunodeficiency
- How many people
- 14 participants
- Where
- 1 siteUnited States
- Study dates
- Oct 2006to Jul 2015
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 40 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Healthy Adult Research Participants
Who may be able to join
- Age greater than or equal to 18 years and less than or equal to 40.
- Meets donation criteria for autologous blood donors per SJCRH Blood Donor Center standard operating procedure.
- Adequate venous access for apheresis on examination as per the judgment of the Blood Donor Center nursing staff, physician staff or physician investigators.
Who cannot join
- Females - lactating.
- Concurrent use of systemic medications that in the judgment of the physician investigators adversely affect platelet function, such as aspirin or non-steroidal antiinflammatory agents.
- Any of the following diagnoses (prior or current):
- pulmonary disease.
- inflammatory disorder.
- coronary artery disease.
Show all 20Show fewer
- stroke (cerebral vascular accident).
- hypertension.
- cardiac arrhythmias.
- venous thrombosis.
- pulmonary embolus
- hematological disease.
- eczema or psoriasis.
- Additional eligibility criteria (to be obtained after signing informed consent)
- Body mass index less than 30 kg/m2.
- No hepatomegaly or splenomegaly.
- Hemoglobin greater than or equal to 12.5 g/dL.
- Platelet count greater than or equal to 150,000/mm3.
- Total WBC > 4200/ul and neutrophil count >1800/ul.
- Females - not pregnant (negative serum or urine; to be obtained after signing informed consent).
Trial locations and contacts
1 site in 1 country.
United States1 site
St. Jude Children's Research Hospital
Memphis, Tennessee, 38105
About this study
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.
Read the 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 CD34+cells 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 e.g., 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.
- Conditions
- Immunodeficiency
- Keywords
- gene transfer
- Medical subject headings
- Immunologic Deficiency Syndromes
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Immunodeficient mice | Please see the Study Description for complete information. |
What is being measured
The primary outcome is the main question the study is designed to answer.
To compare the relative efficiencies of lentiviral and foamy virus vectors in transducing primitive hematopoietic cells mobilized into peripheral blood by cytokine administration.
Measured: Up to 3 years after apheresis collection of donor cells.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Sep 2008 (estimated)
- Study startOct 2006
- Primary completionJul 2015
- Study completionJul 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ImmunodeficiencyStudies of the same condition, open and under way.
- More trials run by St. Jude Children's Research HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 14 participants (actual)
Sponsor and investigators
- Lead sponsor
- St. Jude Children's Research Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- National Heart, Lung, and Blood Institute (NHLBI), Doris Duke Charitable Foundation
- Responsible party
- Sponsor
- Investigators
- Arthur W Nienhuis, MD, Principal investigator, St. Jude Children's Research Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00758992
- Sponsor's protocol ID
- PBSCRV
- Other IDs
- P01HL053749, 2010037
- Status last verified
- Mar 2016
- First submitted
- 18 Sep 2008
- Last updated
- 14 Mar 2016
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 14 Mar 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT00758992
- Acronym / sponsor ID
- PBSCRV
- Conditions
- Immunodeficiency
- Keywords
- gene transfer
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 14 participants (actual)
- Lead sponsor
- St. Jude Children's Research HospitalUniversity, hospital or other
- Collaborators
- National Heart, Lung, and Blood Institute (NHLBI), Doris Duke Charitable Foundation
- Study start
- Oct 2006
- Primary completion
- Jul 2015 (actual)
- Study completion
- Jul 2015 (actual)
- First posted
- 25 Sep 2008 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 CD34+cells 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 e.g., 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 design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Immunodeficient mice | – | –Please see the Study Description for complete information. |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Healthy Adult Research Participants
Key inclusion criteria (3 listed)
- Age greater than or equal to 18 years and less than or equal to 40.
- Meets donation criteria for autologous blood donors per SJCRH Blood Donor Center standard operating procedure.
- Adequate venous access for apheresis on examination as per the judgment of the Blood Donor Center nursing staff, physician staff or physician investigators.
Key exclusion criteria (20 listed)
- Females - lactating.
- Concurrent use of systemic medications that in the judgment of the physician investigators adversely affect platelet function, such as aspirin or non-steroidal antiinflammatory agents.
- Any of the following diagnoses (prior or current):
- Additional eligibility criteria (to be obtained after signing informed consent)
- Body mass index less than 30 kg/m2.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
To compare the relative efficiencies of lentiviral and foamy virus vectors in transducing primitive hematopoietic cells mobilized into peripheral blood by cytokine administration.
Time frame: Up to 3 years after apheresis collection of donor cells.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Mar 2016.
- St. Jude Children's Research HospitalLink provided by the sponsor.
- Clinical Trials Open at St. JudeLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Arthur W Nienhuis, MD principal investigator
St. Jude Children's Research Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Immunodeficiency, run by St. Jude Children's Research Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 20 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Mar 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To compare the relative efficiencies of lentiviral and foamy virus vectors in transducing primitive hematopoietic cells mobilized into peripheral blood by cytokine administration. (time frame: Up to 3 years after apheresis collection of donor cells.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Mar 2016.