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临床试验/NCT01429038
NCT01429038已完成1 期

Infusion of Third-party Mesenchymal Stem Cells After Renal or Liver Transplantation. A Phase I-II, Open-label, Clinical Study

University of Liege2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2012年2月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
2
主要终点
Infusional toxicity

研究概览

简要总结

The immune system of a patient can attack the liver or the kidney received from a donor (organ rejection). This can be prevented by treating these patients long-life with immunosuppressive drugs. Unfortunately, these drugs lead to numerous side effects and fail to prevent the rejection occurring months later after the transplantation (chronic rejection). Recently, it has been shown that a particular type of cells present in the bone marrow, namely Mesenchymal Stem Cells (MSC), when injected to a patient, suppress its immune system and increase success rates of blood cells transplantation. This outcome opens doors to investigate the potential of these cells to provide a valuable tool for improving solid organ transplantation without the need of high concentration of immunosuppressive drugs. The present project aims at evaluating the safety and tolerability of MSC administration after liver or kidney transplantation.

详细描述

The present project aims at evaluating the safety and tolerability of third party MSC administration after liver or kidney organ transplantation. Ten patients undergoing liver transplantation and 10 patients undergoing kidney transplantation will be included in the experimental arm to receive a single infusion of MSC. The outcome of each of these 2 subgroups will be compared with that of similar control patients undergoing liver or kidney transplantation but who will not receive MSC.

Liver and kidney transplanted patients will receive standard immunosuppressive therapy, TAC-MMF-steroïds and TAC-MMF-steroïds plus an IL-2-R antibody respectively. Patients enrolled in the experimental arms will be infused with a single dose of 1,5-3,0 10E6 MSC/kg, 3(+/-2) days after the transplantation.

Weaning of immunosuppression will be attempted from month 6 in liver transplant patients who did not present a rejection episode and show normal graft function and graft biopsy.

Kidney transplant patients will continue standard immunosuppressive therapy indefinitely.

Male or female (>18 years) individuals unrelated to the recipient or the graft donor will be MSC donors. MSC donors need to fulfill generally accepted criteria for allogeneic HSC donation.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients between 18 and 75 years of age, who will undergo first Kidney Transplantation or whole Liver Transplantation from a cadaveric or donation after cardiac death (DCD) organ donor;
  • Fertile female patients must use a reliable contraception method;
  • Informed consent given by patient or his/next of kin if the patient is unable to give informed consent, for the complete (MSC + follow-up) or partial(no MSC + follow-up) study;
  • Successful liver/kidney transplantation, demonstration of organ function (improvement of INR in liver recipients and of creatinine in kidney recipients at 24-36h) and normal graft vasculature at Doppler examination.

排除标准

  • Past history of malignant disease, with the exception of hepatocarcinoma within the Milan criteria for the Liver Transplantation patients;
  • Active uncontrolled infection;
  • HIV or HCV positive;
  • EBV-negative;
  • Retransplantation;
  • Combined transplantation;
  • Living related transplantation or split liver transplantation;
  • Autoimmune disease or expected impossibility to wean immunosuppression (Liver Transplantation) or corticosteroids (Kidney Transplantation);
  • Endotracheal intubation;
  • Postoperative cardiovascular instability, active hemorrhage, or any other serious clinical complication between transplantation and evaluation for suitability for MSC infusion;
  • For Kidney Transplantation: panel reactive antibodies (PRA) >50%.

研究组 & 干预措施

MSC Kidney Transplantation

Experimental

Patients undergoing a first kidney transplantation. Beside receiving standard kidney tranplantation care (antibacterial and viral prophylactic treatments as well as a standard immunosuppressive regime i.e. tacrolimus, mycophenolate mofetil and steroids associated with ant-IL-2 antibodies), patients will be infused with 1,5-3,0 10E6 MSC/kg on postoperative day 3+/-2.

干预措施: Mesenchymal Stem Cells (Biological)

MSC Liver Transplantation

Experimental

Patients undergoing a first liver transplantation. Beside receiving standard liver tranplantation care (antibacterial and viral prophylactic treatments as well as a standard immunosuppressive regime i.e. tacrolimus, mycophenolate mofetil and steroids), patients will be infused with 1,5-3,0 10E6 MSC/kg on postoperative day 3+/-2

干预措施: Mesenchymal Stem Cells (Biological)

结局指标

主要结局

Infusional toxicity

时间窗: Within 24 hours of infusion

Incidence, timing and severity of any clinical complication related to MSC infusion, including pulmonary events or immune reactions.

Incidence of infections (bacterial, viral, fungal, parasitic) and cancers

时间窗: Continuously over 2 years

* Incidence, timing and severity of any infection (bacterial, viral, fungal, parasitic) (blood hemoculture, urine culture, PCR CMV, PCR BK virus at month 1,2,3) * Incidence, timing and severity of malignant disease (Posttransplant lymphoproliferative disorder or other)

次要结局

  • Patient and graft survivals(Continuously over 2 years)
  • Effects of MSC on graft function(over 1 year)
  • Feasibility and safety of weaning or decreasing immunosuppression(continuously over 2 years)
  • Recipient's immune function(over 1 year)
  • Biopsy-proven (Banff classification) rejection rates(over 1 year)
  • Anti-MSC donor HLA antibodies.(over 1 year)

研究者

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

Yves Beguin

Prof

University of Liege

研究点 (2)

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