Prakt. lékáren. 2010; 6(2): 84-86
Successful kidney transplantation depends on the quality of the donor organ, surgical procedure and immunosuppressive regimen. Immediately
before and shortly after transplantation, induction immunosuppression is used, based on T lymphocyte depletion or blockade
of function. In patients at risk of rejection, antithymocyte globulin is used while, in patients at low risk, monoclonal antibody basiliximab
against interleukin-2 receptor is used. Long-term immunosuppression mostly consists of a combination of calcineurin inhibitor (tacrolimus
or cyclosporin A) together with mycophenolate mofetil, an inhibitor of purine synthesis, and steroids. When there is a history of malignancy,
alternative treatment with proliferation signal inhibitors (sirolimus or everolimus) comes into question. When rejection occurs, steroid
pulses are used; if this treatment fails, antithymocyte globulin is used. Long-term immunosuppression is burdened with the occurrence of
a number of adverse effects, including infection, cardiovascular complications, nephrotoxicity and tumours. New promising nonnephrotoxic
immunosuppressants include belatacept, a fusion protein. The other new molecules are currently subject to clinical trials.
Published: May 1, 2010 Show citation
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