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临床试验/NCT02061215
NCT02061215终止不适用

Effects of Age on Immune Risk Profile in CMV Seropositive Kidney Transplant Recipients After Release From CMV Prophylaxis

University of Nebraska1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2014年4月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
7
试验地点
1
主要终点
CMV viral loads in older seropositive kidney transplant recipients before transplant, during treatment and after therapy

研究概览

简要总结

Using novel CYTOF technology to measure a wide array of innate and adaptive cell proportions and cytokine levels, we plan a pilot study in old (>/=60 years) and young (20-40 years) renal transplant recipients who are cytomegalovirus (CMV) seropositive (regardless of donor serology). Viral load measurements will be performed at baseline prior to transplant (within 1 week),and then at 3, 7 and 10 months after transplant. It is expected that the patient will receive anti-CMV prophylaxis until 6 months post-transplant, so the latter two time points will reflect responses after "release" from antiviral suppression. Each patient will serve as their own control, with comparisons made between measurements at baseline and then at each timepoint. In addition, clinical data will be collected at the time points indicated, particularly renal function and the presence/absence of acute rejection.

详细描述

Using novel CYTOF technology to measure a wide array of innate and adaptive cell proportions and cytokine levels, we plan a pilot study in old (>/=60 years) and young (20-40 years) renal transplant recipients who are CMV seropositive (regardless of donor serology). Viral load measurements will be performed at baseline prior to transplant (within 1 week),and then at 3, 7 and 10 months after transplant. It is expected that the patient will receive anti-CMV prophylaxis until 6 months post-transplant, so the latter two time points will reflect responses after "release" from antiviral suppression. Each patient will serve as their own control, with comparisons made between measurements at baseline and then at each timepoint.

Blood from 10 patients in each age group will be studied, to collect virologic and immune response data:

  • CYTOF (broad array of measurements)
  • Tetramer assays (requires recipient HLA type of A1, A2, B7)
  • CMV viral load PCR
  • Response to pneumococcal antigens and inactivated influenza virus

In addition, clinical data will be collected at the time points indicated,particularly renal function and the presence/absence of acute rejection.

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
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults young age 20-40 years and old >/= 60 years
  • Anticipate renal transplant within 2 weeks
  • CMV sero-positive renal transplant recipients
  • HLA type of A1, A2, B7 of recipient

排除标准

  • Pediatric recipients
  • Multi-organ transplant recipients
  • Highly sensitized (antigen level) recipients
  • Prior organ transplant recipients
  • Patients who do not wish to participate in study, or who cannot consent to research
  • Patients with active CMV infection
  • Seronegative
  • HLA Type of organ recipient not corresponding to A1,A2, B7

结局指标

主要结局

CMV viral loads in older seropositive kidney transplant recipients before transplant, during treatment and after therapy

时间窗: 1 year

CMV viral loads in older (age \>/= 60) seropositive kidney transplant recipients before renal transplant, during treatment with anti-viral therapy, and after release from therapy

CMV viral loads in younger seropositive kidney transplant recipients before transplant, during treatment and after therapy

时间窗: 1 year

CMV viral loads in younger (age 20-40) seropositive kidney transplant recipients before renal transplant, during treatment with anti-viral therapy, and after release from therapy

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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