“…[36][37][38] In another study, which used prospectively dose-adjusted ATG induction therapy based on immunologic risk, there were excellent and equivalent short and long-term survival rates, with a low incidence of cellular and antibodymediated rejection. 39 Other potential benefits of r-ATG in HT may include lower risk of ischemia-reperfusion injury, 40 reduced coronary plaque progression (as assessed by intravenous ultrasound) within the first year after transplant, 41 and prolonged effect on LD, lasting 6 months or longer. 42 In renal transplantation, a larger randomized trial with 278 high-risk patients found that r-ATG (cumulative dose, 7.5 mg/kg) achieved a significantly lower rate of acute rejection (15.6% vs 25.5%) and antibody-treated rejection (1.4% vs 8.0%) compared with IL-2RA induction, although graft survival, delayed graft function, and patient survival were unaffected.…”