Plasmapheresis-resistant acute humoral rejection successfully treated with anti-C5 antibody

Pediatr Transplant. 2014 Feb;18(1):E1-5. doi: 10.1111/petr.12187. Epub 2013 Nov 25.

Abstract

Even if kidney graft survival has improved during the last decades, sensitized pediatric patients are an emerging problem. We describe a 17-yr-old male who lost his first graft due to chronic rejection becoming hyperimmunized (CDC PRA 99.61%). A desensitization protocol based on high-dose IVIG, PP, and two Mabthera(®) infusions was performed with minor response (CDC PRA post-desensitization 80%). One month after his second non-living transplant, he developed a biopsy-proven AMR; post-transplant immunological monitoring showed the presence of donor-specific anti-DQ5 antibodies (DSA, MFI 20.000). He received methylprednisolone pulses and 45 PP sessions without clinical response; eculizumab was then used to salvage a kidney undergoing severe PP-resistant rejection. A biopsy performed after the fourth eculizumab infusion showed complete resolution of AMR. Eculizumab infusions were then continued for the first year post-transplantation. Two yr after transplantation, graft function is stable. Anti-C5 therapy may represent an effective therapeutic option in pediatric patients with PP-resistant AMR.

Keywords: eculizumab; pediatric; plasmapheresis; sensitized transplant recipient.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Antibodies / chemistry*
  • Antibodies, Monoclonal, Humanized / administration & dosage
  • Complement C5 / immunology
  • Graft Rejection / therapy*
  • Graft Survival
  • Humans
  • Immunity, Humoral*
  • Kidney Failure, Chronic / therapy
  • Kidney Transplantation
  • Male
  • Methylprednisolone / administration & dosage
  • Nephrotic Syndrome* / congenital
  • Nephrotic Syndrome* / therapy
  • Plasmapheresis
  • Treatment Outcome

Substances

  • Antibodies
  • Antibodies, Monoclonal, Humanized
  • Complement C5
  • eculizumab
  • Methylprednisolone