In recent years, many new immunosuppressive drugs have been discovered and
developed for clinical use in transplantation. This review focuses on those
drugs (leflunomide, mycophenolate mofetil, sirolimus, tacrolimus) that hav
e been shown to have immunosuppressive activity in patients. Different anti
-interleukin-2 receptor antibodies are also reviewed as an example of a res
urgence of development in the area of monoclonal antibodies. The price for
reducing the incidence of allograft rejection by improved immunosuppression
was thought to be a proportional increase in the incidence of infection an
d malignancy. Data from Phase III clinical trials of new immunosuppressants
, however, show a statistically significant reduction in the incidence of a
cute rejection produced by these new drugs, which has not been accompanied
by increases in infection and malignancy rates. The wide array of new drugs
offers the opportunity to use combinations that block different pathways o
f immune activation while at the same time selecting drug combinations with
nonoverlapping toxicity profiles so that doses of each single drug call be
reduced below toxicity levels. The immunosuppressive therapy for patients
can be tailored according to their individual needs.