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Accelerated Immunosenescence and Chronic Kidney Disease

Accelerated Immunosenescence and Chronic Kidney Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02116270
Acronym
IRIS
Enrollment
222
Registered
2014-04-16
Start date
2013-09-30
Completion date
2017-01-31
Last updated
2018-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal Failure

Keywords

Renal Failure, Dialysis, Biological Aging

Brief summary

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

Detailed 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.

Interventions

BIOLOGICALBlood sample

3 tubes of 5 ml tubes and 4 of 7 ml for biological assays at t0.

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Cluster of Differentiation (CD) 4/8+ CD 57+ CD 28- lymphocytes (senescent lymphocytes)6 monthsThe 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.

Secondary

MeasureTime frameDescription
Telomerase Activity of T lymphocytes6 monthsThe telomerase activity of T lymphocytes is assessed by a method of Polymerase chain reaction (PCR)-ELISA.
Level of phospho-histone 2AX (gH2AX) in peripheral blood T lymphocytes6 monthsThis level is obtained by flow cytometry after permeabilization and labelling of Peripheral Blood Mononuclear Cells (PBMC).
Proportion of Recent Thymic Emigrants (RTE) in peripheral blood T lymphocytes6 monthsRTE T cells will be defined by flow cytometry, according to co-expression of CD 4, CD 8,CD 31 and CD 45RA
T-cell receptor excision circle (TREC) level in PBMC.6 monthsTRECs study is based on a technique of quantitative PCR using DNA extracted from PBMC.
Telomere length in T lymphocytes6 monthsStudy 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.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026