Polyclonal Regulatory T Cell (PolyTreg) Immunotherapy in Islet Transplantation
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 11
- 试验地点
- 1
- 主要终点
- Adverse Events
研究概览
简要总结
Islet transplantation is a relatively new procedure used in people with difficult to control Type 1 diabetes. Patients who receive an islet transplant take medication that suppresses their immune system and prevent rejection of the islet tissue. In spite of the strengths of the current immunosuppression regimen, it has failed to enhance single-donor success rates, and the majority of patients require 2 or more islet transplants to achieve insulin independence. The need for life-long, high-dose immunosuppression is also associated with substantial side effects, and continues to limit application of islet transplantation earlier in the course of the disease.
The investigators have learned that Regulatory T cells (Tregs), a small subset of cluster of differentiation 4+ (CD4+) T cells, have emerged as the major contributor to self-tolerance through suppression of activation and effector function of other immune cells. Tregs function by preventing the initiation of unwanted immune activation and by suppressing ongoing immune response to limit bystander tissue destruction. It has been suggested that infusion of Tregs before extensive graft damage may improve long-term graft outcomes.
This study is an open label, controlled, dose finding pilot study. Up to 18 participants will be recruited including 12 participants receiving the investigational treatment and 6 participants being assigned to control group. All participants will undergo the routine Standard of Care islet transplant procedure, and will be maintained on lower dose tacrolimus and sirolimus immunosuppression.
The primary goal is to assess the safety and feasibility of intravenous infusion of ex vivo-selected and ex vivo-expanded autologous PolyTregs in islet transplant patients. The other goal is to assess the effect of Tregs on beta cell function in islet transplant patients.
The control group (6) will receive the current Edmonton islet transplant induction therapy (Alemtuzumab with Etanercept and Anakinra). The intervention group (up to 12) will receive islet transplant with same induction therapy as control group and PolyTregs (400-1600 million) six weeks post- transplant and will be followed for 1 year to assess safety and preliminary efficacy of Treg therapy. The Treg product will be administered via a peripheral intravenous (IV) line primed with saline per established standard operating procedures in approximately 20 to 30 minutes. The intravenous line will be maintained after the infusion and the participant will be asked to remain in the hospital for 24 hours. All participants will be maintained on low dose tacrolimus and sirolimus immunosuppression.
The investigators will also use retrospective data from the islet transplant cohort receiving Tac/mycophenolate mofetil(MMF) with alemtuzumab (>100 patients).
All study participants will be followed up for 58 weeks. Tests and assessments will be performed at each key study visit and will be allowed for +/- 2 weeks to accommodate scheduling.
The following measurements will be recorded at each key study visit :
Blood work, including the following:
Complete blood count (CBC) and differential
Creatinine and electrolytes
Fasting glucose and c-peptide
Any adverse events
Physical examination
Body weight (kg)
Vital signs (BP, HR)
Glucose records for self-monitoring.
Hemoglobin A1c
Insulin use (total daily dose)
Autoantibodies and autoreactive T cell
MMTT
Immune profile
详细描述
BACKGROUND:
Type 1 diabetes mellitus (T1DM) is an autoimmune disease characterized by the destruction of pancreatic beta (β)-cells, resulting in absolute deficiency of insulin. To date, clinical islet transplantation is an accepted modality to treat select patients who exhibit frequent hypoglycemic events and severe glycemic liability. The "Edmonton Protocol" became a milestone by reporting sustained C-peptide production and high rates of insulin-independence after transplant in patients with T1DM. Due to the challenges associated with allo- and autoimmunity in islet transplantation, appropriate immunosuppression is necessary to prevent acute and/or long-term rejection. Current immunosuppression protocols used in Edmonton and many other international sites for islet transplantation consist of a combination of induction, anti-inflammatory and maintenance therapy, accounting for higher success rates of islet transplantation. In spite of the strengths of the current immunosuppression regimen described above, it has failed to enhance single-donor success rates (15%), with the majority of patients requiring 2 or more islet transplants to achieve insulin independence. In Edmonton, clinical trials are designed to improve islet isolation, engraftment and long-term graft survival. The need for life-long, high-dose immunosuppression is associated with substantial side effects, and continues to limit application of islet transplantation earlier in the course of the disease.
Regulatory T cells (Tregs) are a small subset of CD4+ T cells that depend on the FOXP3 transcription factor for their lineage differentiation and function. Tregs have emerged as the major contributor to self-tolerance through suppression of activation and effector function of other immune cells. Tregs function by preventing the initiation of unwanted immune activation and by suppressing ongoing immune responses to limit bystander tissue destruction. It has been suggested that infusion of Tregs before extensive graft damage may improve long-term graft outcomes. Unlike generalized immunosuppressive regimens, Tregs are long-lived and can function in a dominant and antigen-specific manner. Thus, therapeutic infusion of Tregs has the potential to induce long-term donor-specific tolerance without impeding desired immune responses to pathogens and tumors in transplant patients. In terms of diabetes, both animal and human studies demonstrate the central role of Tregs in preserving β-cell function. Infusion of Tregs prevents and even reverses diabetes in non-obese diabetic (NOD) mice. It has been demonstrated in animal studies that infused Tregs migrate to the allograft site shortly after transplantation and can induce stable islet graft survival without immunosuppression. Recent human studies report functional defects of Tregs in T1DM, which appear to be reversible.
This clinical trial is collaboration between Dr. Shapiro's Clinical Islet Transplantation Program team in Edmonton, Alberta with Drs. Tang and Bluestone's teams at the University of California San Francisco (UCSF). Drs. Tang and Bluestone have been instrumental in developing PolyTreg technology, providing an opportunity for this exciting collaboration in a clinical trial of Treg infusion in islet transplantation. Dr. Tang's team focuses on translating knowledge on mechanisms of immune tolerance into novel therapeutics for treating autoimmune diabetes and preventing transplant rejection. They have demonstrated the efficacy of Tregs at multiple levels to halt tissue destruction in diabetic mouse models by subverting fully differentiated effector T-cells. Dr. Bluestone's research over the past 25 years has focused on understanding the basic processes that control T-cell activation and immune tolerance in autoimmunity and organ transplantation including a special emphasis on Tregs. Dr. Bluestone has demonstrated that PolyTreg immunotherapy can be safely administered in adult patients with new onset T1DM. Drs. Tang and Bluestone have abundant experience in Treg isolation and production and Treg immunotherapy, and bring strong technical and scientific support to this project. The investigators expect that this collaboration will integrate the strengths of both Treg immunotherapy and the standard treatment for islet transplant. Hence, this trial is to investigate the safety and efficacy of Treg infusion incorporated into the current protocol for islet transplantation, in the hope of finding more effective alternatives to the current immunosuppression regimen in islet transplantation.
TRIAL DESIGN
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 68 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •To be eligible, subjects must be 18-68 years old, and have had T1DM for more than 5 years, complicated by at least 1 of the following situations that persist despite intensive insulin management efforts:
- •Reduced awareness of hypoglycemia, as defined by the absence of adequate autonomic symptoms at plasma glucose levels < 3.0 mmol/L, indicated by, 1 or more episodes of severe hypoglycemia requiring third party assistance within 12 months, or a Clarke score ≥4, or HYPO score ≥1000, or lability index (LI) ≥400 or combined HYPO/LI >400/>
- •Metabolic instability, characterized by erratic blood glucose levels that interfere with daily activities and or 1 or more hospital visits for diabetic ketoacidosis over the last 12 months.
- •In addition, participants must be capable of understanding the purpose and risks of the study and must sign a statement of informed consent.
排除标准
- •Patients will be excluded if they meet any one or more of the following criteria:
- •Severe co-existing cardiac disease, characterized by any one of these conditions: (a) recent myocardial infarction (within past 6 months); (b) left ventricular ejection fraction <30%; or (c) evidence of ischemia on functional cardiac exam
- •Active alcohol or substance abuse (must be abstinent for 6 months prior to transplant)
- •Clinical history of T1DM diagnosed >age 40, insulin dependent <5 years
- •Active infection including Hepatitis C, Hepatitis B, HIV, tuberculosis (TB) (subjects with a positive purified protein derivative (PPD) performed within one year of enrolment, and no history of adequate chemoprophylaxis)
- •Measured glomerular filtration rate (GFR) < 60mL/min/1.73 m2
- •Presence or history of macroalbuminuria (>300 mg/g creatinine)
- •Clinical suspicion of nephritic (hematuria, active urinary sediment) or rapidly progressing renal impairment (e.g. Increase in serum creatinine of 25% within the last 3-6 months)
- •Baseline Hb < 105g/L (<10.5 g/dL) in women, or < 120 g/L (<12 g/dL) in men
- •Untreated proliferative retinopathy
- •Positive pregnancy test, intent for future pregnancy, failure to follow effective contraceptive measures, or presently breast-feeding
- •Previous transplant or evidence of significant sensitization on panel reactive antibody (PRA) (at the discretion of the investigator).
- •Insulin requirement >1.0 U/kg/day
- •HbA1C >12%
- •Uncontrolled hyperlipidemia [fasting LDL cholesterol > 3.4 mmol/L (133 mg/dL), treated or untreated; and/or fasting triglycerides > 2.3 mmol/L (90 mg/dL)]
- •Under treatment for a medical condition requiring chronic use of steroids
- •Use of coumadin or other anticoagulant therapy (except aspirin) or subject with PT-INR > 1.5
- •Untreated Celiac disease
- •Patients with a Graves disease will be excluded unless previously adequately treated with radioiodine ablative therapy
研究组 & 干预措施
Treatment
Participants in this arm receive PolyTregs infusion at week 6 post islet transplant.
干预措施: PolyTregs (Biological)
结局指标
主要结局
Adverse Events
时间窗: 58 weeks
Any adverse event that occurs during the study
次要结局
- Stimulated C-peptide level(Week 58 post islet transplant)