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TBase - an Integrated Electronic Health Record and Research Database for Kidney Transplant Recipients
Published on: April 13, 2021
Review of symposium. Sirolimus in kidney transplantation
1Renal, Dialysis and Transplant Unit, Department of Emergency and Organ Transplant, University of Bari, Bari, Italy. fp.schena@nephro.uniba.it
Abstract:
Sirolimus (SRL) is a non-nephrotoxic immunosuppressive drug blocking T-cell proliferation through mTOR inhibition. SRL can be used as (1) an early drug in a calcineurin inhibitor-free protocol in the first 3 months after transplantation, (2) in the early and late conversion protocols as suggested by the multicenter randomized CONVERT trial, and (3) in recipients from marginal donors, because calcineurin inhibitors can increase the preexisting renal damage induced by age, hypertension, and diabetes that are frequent in elderly cadaveric donors. In any case, SRL should be used in patients with a cutoff of proteinuria (
Insights
Sirolimus (SRL), a mTOR inhibitor, offers a non-nephrotoxic immunosuppression option. It is suitable for early post-transplant protocols, conversion therapy, and marginal donor recipients, provided proteinuria is controlled.
Area of Science:
- Immunology
- Nephrology
- Pharmacology
Background:
- Sirolimus (SRL) is an immunosuppressive drug that inhibits T-cell proliferation via mTOR pathway.
- Calcineurin inhibitors (CNIs) can exacerbate renal damage in patients with risk factors like age, hypertension, and diabetes.
Purpose of the Study:
- To outline the potential applications of Sirolimus (SRL) in immunosuppressive protocols.
- To define patient selection criteria for Sirolimus (SRL) therapy based on proteinuria levels.
Main Methods:
- Review of clinical applications of Sirolimus (SRL) in transplantation.
- Analysis of patient eligibility based on proteinuria and creatinine ratios.
Main Results:
- Sirolimus (SRL) can be used as an early immunosuppressant in CNI-free protocols (first 3 months post-transplant).
- Sirolimus (SRL) is effective in both early and late conversion protocols, as supported by the CONVERT trial.
- The drug is beneficial for recipients of marginal donors, mitigating CNI-induced renal damage.
Conclusions:
- Sirolimus (SRL) presents a valuable non-nephrotoxic alternative to CNIs in specific transplant scenarios.
- Patient selection for Sirolimus (SRL) requires careful assessment of proteinuria, with a recommended cutoff of <=800 mg/24 hr or a protein-to-creatinine ratio <0.11.
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