Anti-MICA antibodies are related to adverse outcome in heart transplant recipients

J Heart Lung Transplant. 2009 Apr;28(4):305-11. doi: 10.1016/j.healun.2009.01.003.

Abstract

Background: The clinical relevance of the post-transplant presence of anti-major histocompatibility complex class I chain-related A (MICA) antibodies as a marker for chronic graft failure in heart transplantation was examined using post-transplant sera from 159 heart transplant recipients. Mean follow-up after transplantation was 7 +/- 4.9 years.

Methods: The sera were screened by Luminex (Luminex Corp, Austin, TX) for MICA antibodies. Samples that tested positive were confirmed using a Luminex MICA single-antigen bead assay. The antigen specificity of the detected antibodies was identified. Outcome parameters were survival, cardiac allograft vasculopathy (CAV), and cellular rejection.

Results: We retrospectively selected 159 patients: 107 with 0 or 1 rejection and 52 with 2 or more acute rejection episodes, of whom 36 (22.6%) had a positive screen for anti-MICA antibodies. In 19 of 36 samples, specific anti-MICA antibodies were confirmed by single antigen assay. The presence of post-transplant specified anti-MICA antibodies in patients' sera was associated with acute rejection (63.2% vs 28.6%, p < 0.01) and CAV (78.9% vs 32.8%, p < 0.01). Multivariate analysis identified anti-MICA positivity as an independent risk factor for the development of CAV.

Conclusions: The results indicate that anti-MICA antibodies may be related to adverse outcome after heart transplantation. Post-transplantation monitoring of anti-MICA antibodies could identify patients with an increased risk for acute rejection and vasculopathy.

MeSH terms

  • Adult
  • Antibodies, Anti-Idiotypic / blood*
  • Antibody Specificity
  • Biomarkers / blood
  • Female
  • Follow-Up Studies
  • Genotype
  • Graft Rejection / epidemiology
  • Heart Transplantation / adverse effects
  • Heart Transplantation / immunology*
  • Heart Transplantation / mortality
  • Heart Transplantation / pathology*
  • Histocompatibility Antigens Class I / blood
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Male
  • Middle Aged
  • Reoperation / statistics & numerical data
  • Retrospective Studies
  • Survival Analysis
  • Survivors
  • Time Factors

Substances

  • Antibodies, Anti-Idiotypic
  • Biomarkers
  • Histocompatibility Antigens Class I
  • MHC class I-related chain A