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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02116270
Other study ID # IRIS API/2012/28
Secondary ID
Status Completed
Phase N/A
First received April 9, 2014
Last updated April 4, 2018
Start date September 2013
Est. completion date January 2017

Study information

Verified date August 2016
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the impact of renal function and dialysis techniques on the percentage of senescent T lymphocytes.


Description:

The immunosenescence is a complex and profound remodeling of the immune system during life. It is mainly due to thymic involution and repeated antigenic stimulation. Kidney disease is associated with a decrease in adaptive immunity as evidenced by the decrease in vaccine response and increased susceptibility to infections, similar to those observed in the elderly population.

However, data on aging of the immune system in chronic kidney disease remains incomplete. Furthermore, the determinants of immunosenescence are not also not known. It is possible that "uremic" factors help explain the phenotypic and functional changes of lymphocytes, as antigenic stimuli associated with repeated bio-compatible materials used in dialysis contact.

The purpose of this study is to describe the phenotypes of the immune system of renal and analyze the determinants of these changes.


Recruitment information / eligibility

Status Completed
Enrollment 222
Est. completion date January 2017
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Patient able to understand the reason of the study

- Patient not opposed to the conservation of biological samples for scientific research

Exclusion Criteria:

- Patient suffering from psychotic illness

- Any history of immunosuppressive therapy (except steroids up to 5mg/day)

- History of cancer (except skin cancer) or treated hematological malignancy

- Infectious episode required hospitalization not older 3 months

- Hepatitis B or C infection

- HIV infection, active or inactive

- For dialysis patients: renal failure on dialysis for less than 3 months and/or have benefited from two techniques for renal replacement therapy in the last 6 months

Study Design


Intervention

Biological:
Blood sample
3 tubes of 5 ml tubes and 4 of 7 ml for biological assays at t0.

Locations

Country Name City State
France Service de néphrologie, CHU de Besançon Besançon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Cluster of Differentiation (CD) 4/8+ CD 57+ CD 28- lymphocytes (senescent lymphocytes) The primary outcome measure is the percentage of CD 4/8+ CD 57+ CD 28- lymphocytes by flow cytometry. The technique used is a 6 colors surface labelling of T lymphocytes to study the T cell senescent population. 6 months
Secondary Telomerase Activity of T lymphocytes The telomerase activity of T lymphocytes is assessed by a method of Polymerase chain reaction (PCR)-ELISA. 6 months
Secondary Level of phospho-histone 2AX (gH2AX) in peripheral blood T lymphocytes This level is obtained by flow cytometry after permeabilization and labelling of Peripheral Blood Mononuclear Cells (PBMC). 6 months
Secondary Proportion of Recent Thymic Emigrants (RTE) in peripheral blood T lymphocytes RTE T cells will be defined by flow cytometry, according to co-expression of CD 4, CD 8,CD 31 and CD 45RA 6 months
Secondary T-cell receptor excision circle (TREC) level in PBMC. TRECs study is based on a technique of quantitative PCR using DNA extracted from PBMC. 6 months
Secondary Telomere length in T lymphocytes Study of telomere length is performed after extraction of DNA from isolated T cells. The length is determined by a quantitative PCR technique relative to a reference gene. 6 months
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