Active management versus minimization of immunosuppressives of BK virus-associated nephropathy after a kidney transplant

Exp Clin Transplant. 2014 Dec;12(6):528-33.

Abstract

Objectives: Thus far, there is no active treatment for BK virus-associated nephropathy after a kidney transplant that has proven to be effective. We sought to assess the effectiveness of treatment with leflunomide, intravenous immunoglobulin, and ciprofloxacin on graft outcome after 1 year compared with a historical group treated with reduced immunosuppressive medications strategy.

Materials and methods: Group 1 (n = 19) was composed of kidney transplant recipients with twice positive BK virus-polymerase chain reaction in urine and blood who underwent graft biopsy to confirm BK virus-associated nephropathy. Once BK virus-associated nephropathy was diagnosed, antimetabolite (mycophenolate mofetil or azathioprine) was changed to leflunomide, and intravenous immunoglobulin and oral ciprofloxacin were given. Group 2 (n = 14) was composed of BK virus-associated nephropathy patients treated conventionally with reduced immunosuppressive medications.

Results: Thirty-three patients were treated, 23 were males (70%), there were 15 were deceased donors (45.5%), 15 were diabetics (45.5%), mean human leukocyte antigen mismatches were 3.76, seven had a zero DR mismatch (21.2%), and 8 were CW7 negative (24.2%). All patients received induction therapy (thymoglobulin in 22 [66.6%]), 7 had delayed graft function (21.2%) and 18 received antirejection therapy before receiving BK virusassociated nephropathy diagnosis (52.9%). Maintenance immunosuppression was prednisolone and mycophenolate mofetil (2 g/d) in 31 patients (94%), and tacrolimus in 13 (39.4%). Tacrolimus was given to 12 patients in group 1 (63.1%), while sirolimus was given to 7 patients in group 2 (50%). One graft was lost in each group by the end of the study, and 1 patient died with functioning graft in group 2.

Conclusions: No significant difference existed in 1-year graft outcomes between treatment of BK virus-associated nephropathy by reduction of immunosuppressive medications or actively by leflunomide, intravenous immunoglobulin, and ciprofloxacin.

Publication types

  • Comparative Study
  • Observational Study

MeSH terms

  • Adult
  • Antiviral Agents / administration & dosage*
  • BK Virus / drug effects*
  • BK Virus / immunology
  • BK Virus / pathogenicity
  • Biopsy
  • Ciprofloxacin / administration & dosage*
  • Drug Substitution
  • Drug Therapy, Combination
  • Female
  • Graft Rejection / immunology
  • Graft Rejection / prevention & control
  • Graft Survival / drug effects
  • Humans
  • Immunoglobulins, Intravenous / administration & dosage*
  • Immunosuppressive Agents / administration & dosage*
  • Isoxazoles / administration & dosage*
  • Kidney / drug effects*
  • Kidney / immunology
  • Kidney / virology
  • Kidney Transplantation / adverse effects*
  • Leflunomide
  • Male
  • Middle Aged
  • Polyomavirus Infections / diagnosis
  • Polyomavirus Infections / drug therapy*
  • Polyomavirus Infections / immunology
  • Polyomavirus Infections / virology
  • Prospective Studies
  • Time Factors
  • Treatment Outcome
  • Tumor Virus Infections / diagnosis
  • Tumor Virus Infections / drug therapy*
  • Tumor Virus Infections / immunology
  • Tumor Virus Infections / virology

Substances

  • Antiviral Agents
  • Immunoglobulins, Intravenous
  • Immunosuppressive Agents
  • Isoxazoles
  • Ciprofloxacin
  • Leflunomide