Clinicopathologic characteristics and outcomes of late acute antibody-mediated rejection in Thai kidney transplant recipients: a single-center experience

Transplant Proc. 2014;46(2):477-80. doi: 10.1016/j.transproceed.2014.01.003.

Abstract

Background: Late antibody-mediated rejection (ABMR) has worse prognosis than early ABMR. The objective of this study was to examine the clinical and pathological features of late acute ABMR in our experience.

Method: We retrospectively reviewed all patients who underwent kidney transplantation (KT) between January 2001 and December 2012. Patients who had glomerulitis and/or peritubular capillaritis on kidney biopsy performed 6 months after KT were enrolled.

Results: Of 592 patients, late acute ABMR was diagnosed in 34 cases (5.74%) with a mean onset of 49.2 ± 30.2 months post-KT. Six patients (17.6%) had nonadherence. Allograft histopathology demonstrated concomitant transplant glomerulopathy in 23 patients (67.6%) and positive peritubular C4d staining in 25 patients (73.5%). Donor-specific antibody (DSA) was detected in 25 patients (73.5%). Anti-HLA class II antibody was more prevalent than class I (67.6% vs 20.6%; P = .003) and most of them were anti-HLA DQ. We prescribed intravenous immunoglobulin (IVIG) 1-2 g/kg for 30 patients (88.2%), plasma exchange (PE) for 27 patients (79.4%), and rituximab 375 mg/m(2) for 18 patients (52.9%). We repeated treatment with PE and IVIG in 12 refractory cases. For clinical outcome, 21 patients (61.7%) had deterioration of graft function; 9 of them (26.5%) eventually lost their graft. Thirteen patients (38.2%) had stable graft function.

Conclusion: Late acute ABMR has unsatisfactory prognosis in spite of aggressive standard antihumoral treatment. Surveillance of late ABMR using DSA monitoring may be helpful in early detection and management.

MeSH terms

  • Adult
  • Antibodies / immunology*
  • Antibodies, Monoclonal, Murine-Derived / therapeutic use
  • Biopsy
  • Female
  • Graft Rejection / immunology*
  • HLA Antigens / immunology
  • Humans
  • Immunoglobulins, Intravenous / therapeutic use
  • Kidney Transplantation*
  • Male
  • Plasmapheresis
  • Rituximab
  • Thailand

Substances

  • Antibodies
  • Antibodies, Monoclonal, Murine-Derived
  • HLA Antigens
  • Immunoglobulins, Intravenous
  • Rituximab