Initial data on basiliximab in critically ill children undergoing heart transplantation

J Heart Lung Transplant. 2005 Sep;24(9):1284-8. doi: 10.1016/j.healun.2004.08.017.

Abstract

Background: More children are coming to heart transplantation on extracorporeal membrane oxygenation (ECMO), or inotropic support and/or with renal impairment. The use of basiliximab, a chimeric monoclonal antibody against CD25 (interleukin 2 receptor alfa) has not been previously reported in critically ill pediatric heart transplant recipients. Basiliximab has potential advantages in the treatment of patients with renal impairment.

Methods: Basiliximab was provided to 29 patients (median age 7.8 years; range 0.4-16 years) on ECMO, with renal impairment or receiving intravenous inotropes at transplantation. Children normally received 2 doses on Day 0 and Day 4 after transplantation. Calcineurin inhibitor was provided in low dose or withheld altogether in patients with renal impairment. Flow cytometry was used to monitor CD25.

Results: At transplantation, 11 patients were prescribed cyclosporine; the remaining 18 received tacrolimus. All but 4 patients had subtherapeutic levels of calcineurin inhibitor in the first postoperative week. Excluding these 4, there were 19 patients who had more than 4 consecutive doses of calcineurin inhibitor canceled in the first week (median 8 doses; range 3-40 doses). A total of 71 surveillance biopsies were performed, and 4 episodes of severe acute rejection occurred in the first 6 months. In all but one child, the glomerular filtration rate had returned to, or improved on baseline measurement by 1 month after transplantation. Infections rates were low and acceptable. CD25 was undetectable at first assessment, and in all but 1 patient (on ECMO) for at least 2 to 3 weeks thereafter. There were no adverse effects.

Conclusions: Basiliximab was well tolerated in this group of very ill children. In children with pre- or postoperative renal dysfunction, where doses of calcineurin inhibitor were low or canceled, basiliximab was associated with a low incidence of rejection. Posttransplant ECMO may reduce the efficacy of basiliximab. These preliminary results are encouraging and now need confirmation in a large, randomized trial.

Publication types

  • Clinical Trial

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adolescent
  • Antibodies, Monoclonal / therapeutic use*
  • Basiliximab
  • Calcineurin / blood
  • Child
  • Child, Preschool
  • Cyclosporine / therapeutic use
  • Extracorporeal Membrane Oxygenation
  • Female
  • Graft Rejection / prevention & control
  • Heart Transplantation* / immunology
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Infant
  • Kidney / drug effects*
  • Kidney / physiopathology
  • Kidney Diseases / complications
  • Male
  • Phosphoproteins / blood
  • Receptors, Interleukin-2 / antagonists & inhibitors
  • Receptors, Interleukin-2 / blood
  • Recombinant Fusion Proteins / therapeutic use*
  • Tacrolimus / therapeutic use

Substances

  • Adaptor Proteins, Signal Transducing
  • Antibodies, Monoclonal
  • CABIN1 protein, human
  • Immunosuppressive Agents
  • Phosphoproteins
  • Receptors, Interleukin-2
  • Recombinant Fusion Proteins
  • Cyclosporine
  • Basiliximab
  • Calcineurin
  • Tacrolimus