Gene Transfer for ADA-SCID Using an Improved Lentiviral Vector (TYF-ADA)
Study Details
Study Description
Brief Summary
Gene transfer for ADA-SCID using an improved lentiviral vector (TYF-ADA)
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This clinical trial will evaluate a safety and efficiency improved lentiviral vector system for delivering a therapeutic gene to patients with severe combined immunodeficiency (SCID) due to a defective adenosine deaminase (ADA) gene. This gene encodes for the adenosine deaminase enzyme, which is essential for the proper growth and function of infection-fighting white blood cells called T and B lymphocytes. Patients who lack this enzyme are vulnerable to frequent and severe infections.
ADA-SCID patients are normally rescued by a bone marrow transplant (BMT) from a matched healthy donor. However, matched donors are difficult to find and donor BMT is associated with high risk. This trial aims to treat ADA-SCID using a safety and efficiency improved self-inactivating lentiviral vector carrying a functional ADA gene to correct the genetic defect. By collecting an individual's stem cells and modifying them with a lentivirus, the gene-corrected cells can be returned to the patient to help produce normal healthy immune cells.The primary objectives are to evaluate the safety of the improved self-inactivating lentiviral vector TYF-ADA, the ex vivo gene transfer clinical protocol and the efficacy of immune reconstitution in patients overcoming frequent infections present at the time of treatment. We will assess the lentiviral gene integration sites and the long-term effect of this gene transfer procedure.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: TYF-ADA-modified autologous stem cells Autologous hematopoietic and/or mesenchymal stem cells transduced with lentiviral vector carrying the ADA gene |
Genetic: TYF-ADA gene-modified autologous stem cells
Infusion of TYF-ADA-modified autologous stem cells at 1~10x10^6 gene-modified cells per kg body weight; or more infusions depending on the circumstances
|
Outcome Measures
Primary Outcome Measures
- Overall survival up to a year [15 years]
Patient will be monitored for overall health condition, including immune cell assessments, blood biochemistry and metabolitic activities, metabolic detoxification, gene-modified cell percentage and vector copy number (VCN) in the blood, and continued follow-up for 15 years.
Secondary Outcome Measures
- 1. Success of immune reconstitution [12 month]
Immunological and metabolic values including all leukocyte counts (ALC), T, B and NK cell counts (CD3, CD4, CD8, CD19, CD56), T cell TREC levels, T cell repertoire diversity, PHA proliferation rate, immunoglobulins and dATP levels will be measured.
- 2. Change of infection status [12 month]
Immune recovery associated with reduction of infection episodes and frequencies, including viral, fungal and bacterial infections will be documented.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Diagnosis of classical ADA-SCID based on:
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A proven defective adenosine deaminase (ADA) gene as defined by direct sequencing of patient DNA.
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T-cell immune deficiency defined as one or more of the following: CD3+ autologous T cells < 300/ul, or less than 50% of normal value for in vitro mitogen stimulation, or absent proliferation in vitro to antigens.
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With severe infections, including but not limited to: pneumonitis; protracted diarrhea requiring total parenteral nutrition; infection with herpes viruses or adenovirus or fungus; disseminated BCG infection.
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No cytogenetic abnormalities (medullary karyotype) and no detection of main rearrangements associated with acute leukemia of children.
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No prior allogeneic stem cell transplantation.
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Life expectancy ≥ 2 months.
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Negative for HIV infection.
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Written, informed consent obtained prior to any study-specific procedures.
Exclusion Criteria:
- None
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Shenzhen Geno-immune Medical Institute | Shenzhen | Guangdong | China | 518000 |
Sponsors and Collaborators
- Shenzhen Geno-Immune Medical Institute
Investigators
- Principal Investigator: Lung-Ji Chang, Ph.D, Shenzhen Geno-Immune Medical Institute
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- GIMI-IRB-18003