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临床试验/NCT06271343
NCT06271343招募中不适用

Non-interventional Single-center Study of the Contribution of DP8α Regulatory T Cells Induced by a Gut Microbiota Bacterium to Kidney Transplant Tolerance.

Nantes University Hospital2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2024年5月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
15
试验地点
2
主要终点
To test the role of donor-specific DP8α Tregs in preventing kidney transplant rejection.

研究概览

简要总结

Prospective experimental study using PBMC from a limited number of adult patients (15) treated at Nantes University Hospital for a kidney transplant from a related living donor.

The study will be carried out on PBMC from both donors and recipients, collected during visits scheduled as part of the clinical management of the donor/recipient pair.

The study will test the hypothesis that DP8α Tregs expressing CD73, whose frequency in blood increases stably after non-rejected kidney transplants, but not when patients have undergone or will subsequently undergo rejection, are enriched in donor-specific cells, which would be a strong argument in favor of a direct role for these Tregs in preventing transplant rejection, through their ability to inhibit immune responses directed against donor alloantigens.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Adult donor-recipient pair.
  • First or second kidney transplant from a related ABO-compatible living donor.
  • BMI < 35 for recipients.
  • Adult patients.
  • Patients weighing over 50 kgs.

排除标准

  • Donor/recipient ABO incompatibility
  • BMI > 35 for recipients

结局指标

主要结局

To test the role of donor-specific DP8α Tregs in preventing kidney transplant rejection.

时间窗: 3 months

Measurement at D0 and 3 months post-transplant, and comparison, of the frequency of DP8a Tregs expressing CD73 among circulating T lymphocytes and the frequency of donor-reactive DP8a Tregs (identified in culture by their proliferative response to donor monocytes and clonal validation of DP8a Treg anti-donor reactivity at the 3-month post-transplant stage.

次要结局

  • Determine whether the increased anti-donor reactivity of the patient's DP8α Tregs after transplantation results from the amplification among them of clones and establish, if possible, the anti-donor reactivity of amplified clones.(3 months)
  • Determine whether clones of DP8α Tregs (reactive or not to donor antigens) are reactive to F. prausnitzii bacteria.(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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