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临床试验/NCT02091232
NCT02091232已完成1 期

Renal Transplantation Followed By Infusion of T-Regulatory Cells Made With Belatacept Ex-Vivo

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2014年5月最近更新:
适应症

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

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

James F. Markmann, MD, PhD

Chief, Division of Transplant Surgery

Massachusetts General Hospital

研究点 (2)

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