Renal Transplantation Followed By Infusion of T-Regulatory Cells Made With Belatacept Ex-Vivo
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 4
- 试验地点
- 2
- 主要终点
- Safety and Feasibility of T Regulatory Cell Infusion in Renal Transplantation
研究概览
简要总结
This research study is for patients who are going to receive a kidney transplant from a living donor. After kidney transplantation, it is necessary for transplant recipients to take "immunosuppressive drugs". These drugs work by preventing the body's immune cells from attacking and "rejecting" the new kidney. Taking these drugs long-term may also cause harm to the transplanted kidney. Therefore, the transplant community is very interested in finding ways to decrease immunosuppressive drug treatment and further reduce the risk of kidney rejection. One method to do so is known as "induction of tolerance", which is when the person who receives a transplant has treatment to make their immune cells tolerant to the donor cells.
In this study, we will try to induce tolerance by mixing recipient cells and their donor's cells together with belatacept, an immunosuppressive drug. Belatacept is a protein that attaches to immune system cells, interferes with the immune response and results in tolerance induction.
After we mix the recipient cells with the donor's cells, we will sort out one particular kind of immune cell, called a regulatory T cell, and inject them back into the recipient. Regulatory T cells are the cells that are affected by induction to reduce rejection of donated organs. This method for inducing tolerance has been used in bone marrow transplantation, but this is the first time it is being done in kidney transplantation.
This study is being conducted as part of a unique collaboration of US and EU centers called The ONE Study. The ONE Study centers have agreed to work together using common protocols and procedures but with each testing their own regulatory population for safety and the ability to promote kidney survival. Sharing data among the participating sites will permit a deeper understanding of how and why some treatments might succeed while others work less well.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Chronic renal insufficiency necessitating kidney transplantation
- •Aged at least 18 years
- •Donor is ABO (Blood type) compatible
- •Key Recipient
排除标准
- •HIV positive, EBV negative, or suffering from chronic viral hepatitis or tuberculosis
- •Previously received any tissue or organ transplant other than planned kidney graft
- •Genetically identical to the prospective organ donor at the HLA loci (0-0-0 mismatch)
- •Panel Reactive Antibodies (PRA) >20%
- •Concomitant malignancy or history of malignancy within 5 years prior to planned study entry (excluding successfully-treated non metastatic basal/squamous cell carcinoma of the skin)
- •Ongoing treatment with systemic immunosuppressive drugs at study entry
结局指标
主要结局
Safety and Feasibility of T Regulatory Cell Infusion in Renal Transplantation
时间窗: 2 Weeks
To examine in living donor renal transplant recipients the safety and feasibility of administering T regulatory cells derived from recipient PBMC stimulated with kidney donor PBMC in the presence of costimulatory blockade with belatacept.
次要结局
- Reduction of Immunosuppression(60 Weeks)
- T-Reg Measurements(2 Years)
研究者
James F. Markmann, MD, PhD
Chief, Division of Transplant Surgery
Massachusetts General Hospital
