Percentage of CD19+ Cells in Peripheral Blood Lymphocytes After Rituximab-Based Desensitization as a Predictor of Acute Antibody-Mediated Rejection in ABO-Incompatible Kidney Transplantation

Transplant Proc. 2019 Jun;51(5):1382-1386. doi: 10.1016/j.transproceed.2019.01.127. Epub 2019 Apr 23.

Abstract

Background: Rituximab (RIT) is effective as a part of the desensitization therapy before ABO-incompatible kidney transplantation (ABOi-KTx), and a single dose of RIT at 375 mg/m2 or less is recommended. However, adequate RIT dose recommendations have not yet been established for individual recipients. Therefore, we evaluated the relationship between the proportion of B cells in peripheral blood and acute antibody-mediated rejection (AAMR).

Methods: Forty-four consecutive ABOi-KTx recipients were enrolled in this retrospective study. Before transplantation, subjects were treated with RIT at various doses, ranging from 65 to 400 mg/body (46-263 mg/m2), followed by plasmapheresis and intravenous immunoglobulin as a desensitization therapy. The percentage of CD19+ cells in the total peripheral blood lymphocytes population (%CD19) was determined the day before transplantation. Transplant recipients were divided into 2 groups according to pretransplant %CD19, as follows: low %CD19 group, ≤ 1.2% (n = 35) and high %CD19 group, > 1.2% (n = 9). The relationship between %CD19 and incidence of AAMR was evaluated, and the predicting factors for AAMR incidence were determined by univariate and multivariate analyses.

Results: The incidence of AAMR was significantly higher in the high %CD19 group than in the low %CD19 group (44.4% vs 5.7%, P = .006). Furthermore, multivariate analysis showed that %CD19 > 1.2% was the only independent factor to predict AAMR, with an odds ratio of 14.31 (P = .038).

Conclusion: High %CD19 values after rituximab administration in ABOi-KTx recipients implies insufficient depletion of B cells, which can lead to AAMR.

MeSH terms

  • Adult
  • Antigens, CD19 / blood*
  • Blood Group Incompatibility / drug therapy*
  • Female
  • Graft Rejection / blood
  • Graft Rejection / immunology
  • Graft Rejection / prevention & control*
  • Humans
  • Immunoglobulins, Intravenous / therapeutic use
  • Incidence
  • Kidney Transplantation / methods*
  • Lymphocytes / immunology
  • Male
  • Middle Aged
  • Plasmapheresis / methods
  • Retrospective Studies
  • Rituximab / administration & dosage*
  • Transplant Recipients

Substances

  • Antigens, CD19
  • Immunoglobulins, Intravenous
  • Rituximab