Chronic renal failure is a major public health problem in industrialized countries, due to its frequency - about 3 million patients in France - and its socio-economic impact. At the end stage of renal failure, renal transplantation is the best treatment, allowing an improvement in patient survival compared to treatment by extra-renal purification. Despite improved immunosuppressive strategies, allograft rejection is common in transplantation - between 15% and 25% in the first year - and is associated with lower renal graft survival. Different risk factors for rejection have been well identified, such as the young age of the recipient or a high number of human leukocyte antigen (HLA) incompatibilities between the donor and the recipient. However, these risk factors do not accurately identify the risk of acute rejection in order to optimize and individualize immunosuppressive strategies. Also, the search for biomarkers to predict allograft tolerance prior to transplant is a major goal in renal transplantation. The onset of acute rejection is caused by the ability of the recipient's T cells to recognize alloantigens. The CD45 molecule is a highly expressed tyrosine phosphatase on the surface of the lymphocytes that plays an important role in the activation of the T cell. Investigators showed that the level of expression of CD45RC on T lymphocytes was associated with the risk of acute rejection. Thus, from a retrospective cohort of 89 renal transplant patients followed, recipients with a high percentage of circulating CD8 lymphocytes expressing high CD45RC (CD45RChigh) before transplant had a 5 to 8-fold higher risk of developing acute rejection of allograft during follow-up (11-year average follow-up) compared to recipients with a low percentage of CD8+CD45RChigh. The purpose of this study is to confirm the first retrospective results on a larger prospective and contemporary regional cohort.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SCREENING
Masking
NONE
Enrollment
150
Blood samples the day of the surgery and 4 times during the next year. Blood samples and histological slides taken at each biopsy and if there is suspicion of rejection of the graft
Dr Anne-Sophie GARNIER
Angers, France
RECRUITINGNumber of patient with acute rejection diagnosis confirmed by anatomopathological analysis of a graft biopsy
Time frame: 12 months
Rate of CD45RC for patient with acute rejection suspicion
acute rejection confirmed or not
Time frame: 12 months
Rate of CD45RC on circulating T lymphocytes
Evolution of the expression of CD45RC in the first year after introduction of immunosuppressive therapy
Time frame: from date of randomization until the date of acute rejection, up to 12 months
Rate of CD45RC on circulating T lymphocytes the day of acute rejection
day of acute rejection
Time frame: 12 months
Rate of CD4, CD8, CD45RA, CD25, CD127, CD19 markers on T cells the day of acute rejection
day of acute rejection
Time frame: 12 months
anti-HLA antibodies' dosage at the time of acute rejection
Time frame: 12 months
cytokines' dosage
describe cytokine profile
Time frame: Day 1
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