Monitoring of circulating antibodies in a renal transplantation population: preliminary results

Transplant Proc. 2012 Nov;44(9):2548-50. doi: 10.1016/j.transproceed.2012.09.072.

Abstract

Background: The presence of circulating antibodies (CA) against human leukocyte antigen (HLA) and major-histocompatibility-complex class I-related chain A (MICA) antigens has been associated with worse renal function and reduced kidney allograft survival. We sought to describe the presence of donor-specific anti-HLA antibodies, non-donor specific antibodies, and antibodies against MICA antigens among a cohort of renal transplant recipients with respect to their evolution effects on renal function and occurrence of an acute rejection episode (AR) after transplantation.

Methods: This prospective study of 22 renal transplant recipients of deceased donor kidneys underwent studies of antibodies before and 3 months after grafting using Luminex technology.

Results: Ten patients (five men and five women) showed preexistent CA. Comparing patients with versus without preformed CA, we did not observe a significant difference in donor and recipient age or gender. Eight patients (80%) with CA had undergone induction treatment with anti-human-activated T-lymphocyte rabbit immunoglobulin and 2 (20%) with basiliximab. There were no differences between groups regarding the incidence of acute rejection episodes (ARE n = 3 each). There was one case of Banff grade IIB ARE in a patient without preexisting CA; the other episodes were low-grade cellular responses. There were no differences in other variables including cold ischemia time, HLA mismatches, panel-reactive antibody levels, number of transfusions, cytomegalovirus infection or renal function at discharge and 3 months later. Retransplantation was the only factor associated with preformed CA. Retransplantation and preformed CA were associated with CA at 3 months after transplantation.

Conclusions: CA monitoring is important for highly sensitized renal transplants, although our experience failed to show a difference in graft survival or renal function in the first 3 months' follow-up.

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Monoclonal / therapeutic use
  • Antilymphocyte Serum / therapeutic use
  • Basiliximab
  • Biomarkers / blood
  • Female
  • Graft Rejection / epidemiology
  • Graft Rejection / immunology
  • Graft Rejection / surgery
  • HLA Antigens / immunology*
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Incidence
  • Isoantibodies / blood*
  • Kidney Transplantation / adverse effects
  • Kidney Transplantation / immunology*
  • Male
  • Middle Aged
  • Monitoring, Immunologic
  • Prospective Studies
  • Recombinant Fusion Proteins / therapeutic use
  • Reoperation
  • Risk Factors
  • Spain / epidemiology
  • Time Factors
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antilymphocyte Serum
  • Biomarkers
  • HLA Antigens
  • Histocompatibility Antigens Class I
  • Immunosuppressive Agents
  • Isoantibodies
  • MHC class I-related chain A
  • Recombinant Fusion Proteins
  • Basiliximab