Apheresis and CD34+ Selection of Mobilized Peripheral Blood CD34+ Cells From Patients With DOCK8 Deficiency, LAD-1, and GATA2 Deficiency
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 7
- 试验地点
- 1
- 主要终点
- To collect blood stem cells from patients with immunodeficiency diseases to test our ability to correct the defects of these cells in the test tube.
研究概览
简要总结
Background:
- Gene therapy is being investigated as a possible treatment for individuals with immunodeficiency diseases or other conditions that make it difficult to fight off infection. Gene therapy avoids problems with donor identification and possible rejection of bone marrow transplant by using the patient s own modified blood cells to help treat the disease. Researchers are interested in collecting stem cells from the blood of individuals with immunodeficiency diseases in order to use the cells to develop potential gene therapy treatments.
Objectives:
- To collect blood stem cells from patients with immunodeficiency diseases tto test our ability to correct the defects of these cells in the test tube.
Eligibility:
- Individuals between 18 and 40 years of age with immunodeficiency diseases.
- Individuals with human immunodeficiency virus (HIV) will not be able to participate in this study.
Design:
- Participants will provide an initial blood sample for disease screening (such as hepatitis B and C, syphilis, or viruses like the Epstein-Barr virus, herpes simplex virus, or toxoplasmosis) and to check kidney and liver function.
- Starting 5 days before blood donation, participants will receive daily injections of a drug called G-CSF (granulocyte colony stimulating factor, or filgrastim), which pushes stem cells out of the bone marrow and into the bloodstream. Participants will receive the injections at the National Institutes of Health Clinical Center.
- On day 5, participants will have a single leukapheresis procedure to collect the stem cells from the blood.
- No additional treatment will be provided as part of this protocol. The cells that are collected will be used fore experiments in the lab and will not be used to treat individuals with these diseases.
详细描述
Background:
Primary immunodeficiency diseases (PID) represent candidate genetic disorders for new therapeutic approaches. Our laboratory is developing new therapies for individuals with PID using autologous CD34+ hematopoietic stem cells (HSC). Newer therapies may circumvent problems with allogeneic HSC transplantation, especially graft rejection and graft-versus-host-disease. We are particularly interested in three PID: Dedicator of CytoKinesis-8 (DOCK8) deficiency, Leukocyte Adhesion Deficiency type 1 (LAD-1), and GATA2 Deficiency. For all three diseases the gene has been cloned. Testing new therapies for these diseases would be considerably enhanced by the acquisition of peripheral blood CD34+ cells from individuals with these immunodeficiency diseases.
Objectives:
To provide a source of filgrastim or filgrastim biosimilar mobilized peripheral blood CD34+ hematopoietic stem cells (HSC) for laboratory research studies for DOCK8 deficiency, LAD-1, and GATA2 Deficiency.
Eligibility:
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •INCLUSION CRITERIA - PATIENT:
- •Individuals age 18-40 years.
- •Diagnosis of DOCK8 deficiency, LAD-1, or GATA2 Deficiency:
- •DOCK8 deficiency
- •Homozygous or compound heterozygous mutations in the DOCK8 gene.
- •Less than 10% CD18 expression on the neutrophil surface.
- •GATA2 Deficiency
- •Deleterious mutation of GATA2 Gene
- •Serum creatinine <1.5 mg/dL.
- •Total Bilirubin < 3mg/dl, ALT and AST < 5X upper limit of normal.
- •Ability to give informed consent.
- •Adequate venous access for peripheral apheresis, or consent to use a temporary central venous catheter for apheresis.
- •Individuals of childbearing age must have a negative urine pregnancy test within one week prior to beginning filgrastim or filgrastim biosimilar administration.
排除标准
- •HIV infection.
- •Chronic hepatitis B or hepatitis C virus infection.
- •History of psychiatric disorder which may compromise compliance with protocol, or which does not allow for appropriate informed consent.
- •Active infection that is not responding to antimicrobial therapy.
- •Pregnant Individuals may not participate per OHSRP SOP.
- •Any Individual who is breastfeeding as the effects of filgrastim or filgrastim biosimilar product on infants is not known.
- •Sexually active individuals capable of becoming pregnant who are unable or unwilling to use effective form(s) of contraception during the 10 days surrounding filgrastim or filgrastim biosimilar product administration and apheresis procedure(s). Effective forms of contraception include one or more of the following: intrauterine device (IUD), hormonal (birth control pills, injections, or implants), tubal ligation/hysterectomy, partner s vasectomy, barrier methods, (condom, diaphragm, or cervical cap), or abstinence. Males on the protocol must use an effective form of contraception at study entry.
- •Presence of active malignancy in another organ system other than the hematopoietic system.
- •Individuals with active pulmonary disease.
- •History of hypertension that is not controlled by medication, stroke, or severe heart disease. Individuals with symptomatic angina will be considered to have severe heart disease and will not be eligible.
- •Other medical contraindications to stem cell donation (i.e., severe atherosclerosis, autoimmune disease, iritis or episcleritis, deep venous thrombosis, cerebrovascular accident).
- •Thrombocytopenia (platelets less than 50,000 per microliter) at baseline evaluation.
- •Individuals receiving experimental therapy or investigational agents.
- •Sensitivity to filgrastim, to E. Coli derived products, or to a biosimilar recombinant protein to filgrastim.
- •Individuals must test negative for transfusion-transmissible infectious agents, including hepatitis B (HBsAg), hepatitis C (anti-HCV), HIV (anti-HIV-1/2).
研究组 & 干预措施
Cohort 1
Patients with DOCK8 deficiency, LAD-1, or GATA2 Deficiency
结局指标
主要结局
To collect blood stem cells from patients with immunodeficiency diseases to test our ability to correct the defects of these cells in the test tube.
时间窗: 5 days
Obtain granulocyte colony stimulating factor mobilized peripheral blood CD34+ hematopoietic stem cells (HSC) by apheresis for laboratory research studies for DOCK8 deficiency, LAD-1, and GATA2 deficiency.
次要结局
未报告次要终点