跳至主要内容
临床试验/NCT02633826
NCT02633826已完成不适用

The Role of Pre-formed Alloreactive T Cells on Acute Rejection Episodes and Long-term Graft Outcome in Patients After Living Donor Renal Transplantation

Martina Sester13 个研究点 分布在 1 个国家目标入组 190 人开始时间: 2015年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
190
试验地点
13
主要终点
graft function

研究概览

简要总结

This investigator-initiated study will analyse the role of pre-formed alloreactive T cells on acute rejection episodes and graft outcome in kidney transplant recipients after living donation.

详细描述

In recipients of solid organ transplants, preformed alloreactive T cells may mediate acute rejections and compromise long-term graft survival. Previous studies on the role of alloreactive T cells in transplantation were hampered by the fact that experimental assays to quantify alloreactivity were technically demanding and not suitable for use in a clinical setting. Based on a recent development of a whole-blood assay, alloreactive T cells may be quantified and characterised within one day. This assay therefore provides the experimental basis to study the development and the role of alloreactive T cells in a clinical setting in patients after renal transplantation. This will be performed in a multicenter study in living donor renal transplant recipients where preformed alloreactivity of the recipient towards the living donor will be determined and associated with standard clinical parameters of graft function and long-term graft outcome on follow-up. In addition, the development of donor-specific antibodies will be analysed after transplantation. If this project was able to provide evidence for a role of alloreactive T cells in acute rejection episodes or long-term graft function, this assay may in future be used to guide individualized immunosuppressive drug treatment early after transplantation. It will thereby aid in distinguishing patients where standard immunosuppressive drug regimens are sufficient from the minor population of patients at high risk for rejection who will benefit from intensified drug regimens.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Written informed consent
  • First or second renal transplantation
  • Living donor renal transplantation
  • Recipient older than 18 years
  • Negative cross match
  • Planed quadruple, Tacrolimus-based (low-dose) immunosuppressive drug regimen (Tacrolimus, 2g MMF starting dose, (methyl)prednisolone according to center practice, basiliximab at day 0 and day 4)
  • Planned start of Tacrolimus (Advagraf®) 3 to 10 days prior to transplantation (trough levels 5-10 ng/ml during the first 3 months, 5-7 ng/ml thereafter)

排除标准

  • Planed T-cell depleting induction therapy
  • Pregnancy
  • Pre-existing, moderate to high dose immunosuppressive medication
  • Pre-existing, severe lymphopenia (< 400/µl)

结局指标

主要结局

graft function

时间窗: 1 year

1-year graft function (estimated glomerular filtration rate)

次要结局

  • Creatinine(1 year)
  • rejection: acute rejection episodes within the first year(1 year)
  • Cystatin C(1 year)
  • proteinuria within the first year(1 year)

研究者

发起方
Martina Sester
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Martina Sester

Univ.-Prof. Dr. Martina Sester

Universität des Saarlandes

研究点 (13)

Loading locations...

相似试验