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临床试验/NCT04747522
NCT04747522进行中(未招募)不适用

SARS-CoV-2 Cellular and Humoral Immune Response Following Vaccination of Kidney Transplant Recipients and Healthy Controls

Oslo University Hospital1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年1月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
150
试验地点
1
主要终点
Cellular immunological response

研究概览

简要总结

None of the vaccines approved, or in clinical trials, have so far been tested on transplanted patients. If they produce an immune response to the Spike protein of SARS-CoV-2 it is unknown how long the protective immunity will last.

Not all immune responses are equal. The investigators will quantify immune cell subsets with flow and mass cytometry analyses to describe the phenotype of responding immune cells, including specific T cells. If not already established, patient human Leukocyte antigen (HLA) genotypes will be typed.

In order to compare the immune responses with healthy individuals a control group of hospital employees will be included and sampled before and after vaccination according to the same time schedules as the kidney transplanted patients.

详细描述

Kidney transplanted patients with post-transplant follow-up visits at the national transplant center in Norway will be included before they are SARS-CoV-2 vaccinated. As a control group the investigators will include blood samples from healthy volunteers (hospital employees) that receive vaccine as first line health care workers.

Baseline blood samples will be obtained before vaccination. The vaccination will be performed according to the national procedures and not necessarily by the hospital. Following vaccination, all patients and controls will have blood drawn 7-10 days as well as 4-6 weeks after the second dose. Depending on the results of the immunity testing the patients and controls may be invited to additional blood sampling up or at specific time points to two years following vaccination.

At each blood sampling and at the time of both vaccinations the systemic exposure of tacrolimus will be assessed in kidney transplanted patients.

All samples will be analyzed with validated assays for SARS-CoV-2 immunoglobulin G (IgG) (anti-receptor binding domain (RBD) spike protein) using ELISA, flow cytometry bead arrays and SARS-CoV-2 neutralization assays or comparable techniques. Cells will be analyzed by flow and mass cytometry for activation and phenotype markers, and with functional assays for responsiveness (e.g. proliferation and cytokine production). Samples will be HLA-typed if HLA-genotype if not already established.

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Patients transplanted with a kidney (only) at least 6 months before vaccination OR healthy volunteer first line health care workers at OUS.
  • Age of 18 years or older (also for controls).
  • Standard immunological risk at transplantation (i.e. no donor specific HLA antibodies (DSA)) and not performed an ABO blood-type-incompatible transplantation.
  • No treatment for rejection episodes the last 6 months before inclusion.
  • Immunosuppressive therapy including tacrolimus, mycophenolate and prednisolone.
  • Stable graft-function the last 6 months.
  • S-creatinine < 200 μmol/L (also for controls).
  • Signed informed consent to participate in the study (also for controls).

排除标准

  • Three or more previous transplantations.
  • Hemoglobin level below 10 g/dL (also for control).
  • Leukopenia defined as total lymphocyte count < 2 X 109 (also for controls).
  • Previous treatment with anti-thymocyte antibodies (ATG) or rituximab.

研究组 & 干预措施

Kidney Transplanted patients

Kidney transplanted patients transplanted at least 6 months prior to SARS-CoV-2 vaccination. Vaccination according to national plan with messenger Ribonucleic acid (mRNA) vaccine

干预措施: SARS-CoV-2 vaccine (Drug)

Healthy controls

Healthy hospital staff receiving SARS-CoV-2 mRNA vaccine as being front line Healthcare workers.

干预措施: SARS-CoV-2 vaccine (Drug)

结局指标

主要结局

Cellular immunological response

时间窗: 1.5 months

IgG antibodies against SARS-CoV-2 spike protein above assay limit of positive sample.

Humoral immunological response

时间窗: 1.5 months

T-cell reactivity against SARS-CoV-2 spike protein, including known mutation in the spike protein.

次要结局

  • Vaccine related side effects(6 months)

研究者

发起方
Oslo University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anders Åsberg

Head of Laboratory

Oslo University Hospital

研究点 (1)

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