Recent advances in immunosuppression have focused on more effective, safer,
and targeted therapies that have resulted in improved short- and intermedi
ate-term renal allograft survival. During the past decade there has been a
marked decrease in acute rejection rates following renal transplantation be
cause of the use of newer immunosuppressive agents. Recent data indicate th
at the average yearly reduction in the relative hazard of graft failure bey
ond I year was 4.2% for all recipients (0.4% for those recipients who had a
n acute rejection episode and 6.3% for those who did not have an acute reje
ction). Despite these improvements the currently available immunosuppressiv
e agents are associated with significant cardiovascular risk factors, an in
creased risk of infection, and the development of malignancies in the long
term. Predictive parameters of donor-specific hyporesponsiveness are needed
so as to allow identification of patients in whom immunosuppressive therap
y can be safely reduced. Immunosuppressive agents that have recently been a
pproved for use in the United Slates and those that are in clinical and pre
clinical studies are discussed.