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Rapamycin and Regulatory T Cells in Kidney Transplantation

Rapamycin and Regulatory T Cells in Renal Transplant Patients: a Two-year Randomized Prospective Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01014234
Enrollment
56
Registered
2009-11-16
Start date
2008-07-31
Completion date
2013-06-30
Last updated
2015-03-25

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

Conditions

Kidney Transplantation

Keywords

Immunosuppressive Agents, Immune system regulation, Regulatory T cells, Rapamycin, Tolerance

Brief summary

The immune system response is mediated by the interaction between the antigen presenting cell (APC), CD4+ T helper cells (Th) and CD4+ CD25+ regulatory T cells, a subgroup of CD4+ T cell which express IL-2 receptor (CD25) and the transcriptional factor foxp3. Regulatory T cell may contribute to the maintenance of tolerance by suppressing the immune response to normal or tumor associated antigens. Regulatory T cell emerge from the thymus during ontogenesis and they represent about 10 % of the peripheral Cd4+ t cells. Rapamycin is one the most use treatment to prevent renal allograft failure. Differently from calcineurin inhibitors (cyclosporine and tacrolimus), that inhibit T-cell activation through the inhibition of calcineurin activation, rapamycin inhibits cellular proliferation by impairing the progression of the cellular cycle, in particular by interaction with mTOR. Recently Battaglia et al. have demonstrated a Treg amplification in murine CD4+ lymphocytes treated with rapamycin in vitro. Aim of the study is to evaluate the effect of different immunosuppressive regimens on regulatory T cell and to verify the hypothesis that rapamycin may induce tolerance in kidney transplanted patients, more than cyclosporine treatment.

Detailed description

It is two years randomised controlled trial in parallel groups. It has been resolved to compare different immunosuppressive regimens: 1. cyclosporine+ mycophenolate+prednisone 2. rapamycin + mycophenolate + prednisone, this treatment should be introduced after one month from renal transplantation. Patient should visited at month 1-6-12-24 from the transplant. During the control we will reported the following data: physical examination, blood test (blood count, creatinin, BUN, immunosuppressive blood concentration, histological response of surveillance renal biopsy), blood pressure, attendant change of current therapy, pathological variation, or any hospitalisation both ordinary or in DH regimen. Moreover in all control visit it will be collected a blood sample for evaluation of regulatory t cells.

Interventions

These patients will undergo maintenance immunosuppressive treatment with cyclosporine + mycophenolate + prednisone according to established clinical practice. The dosage of drugs will be based on evaluations of serum trough levels and it will be adjusted when necessary.

DRUGRapamycin

These patients will undergo maintenance immunosuppressive treatment with rapamycin + mycophenolate + prednisone according to established clinical practice. The dosage of drugs will be based on evaluations of serum trough levels and it will be adjusted when necessary.

Sponsors

Fondazione IRCCS Policlinico San Matteo di Pavia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Male and female aged from 18 to 75 years * Transplanted patients from cadaveric donors * Patients who has given written informed consensus

Exclusion criteria

* Legally unable patients * Patients who have been participated to others studies in the last 3 months * Addicted to alcohol or smoking

Design outcomes

Primary

MeasureTime frame
The absolute number of T-reg after renal transplant in patients in treatment with rapamycin compared to patients treated with cyclosporineEvery 6 months after the transplantation

Secondary

MeasureTime frame
Adverse events developed during the duration of the clinical study, that damage the patient, that is not part of the natural history of the disease.Every two months during the follow-up

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026