Combined use of rituximab and plasmapheresis pre-transplant increases post-transplant infections in renal transplant recipients with basiliximab induction therapy

Transpl Infect Dis. 2013 Dec;15(6):559-68. doi: 10.1111/tid.12135. Epub 2013 Sep 9.

Abstract

Introduction: We investigated the effect of combined use of rituximab (RTX) and plasmapheresis (PP) pre-transplant on post-transplant infection.

Methods: A total of 196 patients undergoing living-donor kidney transplantation at Seoul St. Mary's Hospital, all of whom underwent basiliximab induction therapy, were included in the study. They were divided into 3 groups: RTX/PP/intravenous immune globulin (IVIG) (the RPI group; n = 53), RTX monotherapy (the RTX group; n = 14), and control (the CONT group; n = 129). We compared the post-transplant infections in the 3 groups.

Results: The overall prevalence of infection was significantly higher, and the infection-free survival rate was lower, in the RPI group compared with the RTX or CONT groups (P < 0.05). A trend toward more severe bacterial infections was seen in the RPI group compared with the other groups, and fungal infections developed only in the RPI group. After anti-rejection therapy, a significantly higher rate of infection developed in the RPI group than in the other groups (P < 0.05). In addition, the RPI group was an independent risk factor for the development of infection.

Conclusion: Our results show that in the setting of basiliximab induction, the use of combined RTX and PP therapy pre-transplant significantly increases the risk for post-transplant infection.

Keywords: infectious complication; kidney transplantation; plasmapheresis; rituximab.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Murine-Derived / adverse effects*
  • BK Virus
  • Basiliximab
  • Combined Modality Therapy / adverse effects
  • Cytomegalovirus Infections / etiology
  • Disease-Free Survival
  • Female
  • Graft Rejection / prevention & control
  • Herpes Zoster / etiology
  • Humans
  • Immunoglobulins, Intravenous / therapeutic use
  • Immunologic Factors / adverse effects*
  • Immunologic Factors / therapeutic use
  • Immunosuppressive Agents / therapeutic use
  • Induction Chemotherapy
  • Kidney Transplantation / methods*
  • Lung Diseases, Fungal / etiology
  • Male
  • Middle Aged
  • Plasmapheresis / adverse effects*
  • Pneumonia, Bacterial / etiology
  • Polyomavirus Infections / etiology
  • Preoperative Care / adverse effects
  • Recombinant Fusion Proteins / therapeutic use
  • Retrospective Studies
  • Rituximab
  • Transplantation Conditioning / adverse effects*
  • Tumor Virus Infections / etiology
  • Urinary Tract Infections / etiology

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Immunoglobulins, Intravenous
  • Immunologic Factors
  • Immunosuppressive Agents
  • Recombinant Fusion Proteins
  • Rituximab
  • Basiliximab