In this schema, the decision to use specific immunosuppression regimens is based on known risk factors, including those used currently (living or deceased donor type, recipient race, HLA match, alloantibodies) and emerging biomarkers (genetic polymorphisms and T cell memory) that may alter posttransplant risk of injury. If the recipient develops evidence of graft damage (e.g., proteinuria and/or elevated levels of creatinine), biomarker results and molecular analyses of graft tissue will supplement histopathology to guide specific alterations in therapy aimed at reversing the disease processes. In patients with stable kidney function, biomarker results will ideally differentiate patients with subclinical injury (need more therapy) from patients who need immunosuppression but are not tolerant and from patients who can be safely withdrawn from immunosuppression (operationally tolerant).