Korean J Transplant.  2021 Oct;35(Supple 1):S61. 10.4285/ATW2021.PO-1113.

Combination therapy of low-dose cidofovir and leflunomide in a kidney transplant recipient with BK virus nephropathy: a case report

Affiliations
  • 1Department of Internal Medicine-Nephrology, Bongseng Memorial Hospital, Busan, Korea

Abstract

Background
BK virus frequently results in allograft loss or permanent dysfunction in kidney transplant recipients. It is a challenge to treat BK virus nephropathy (BKVN) because the reduction of immunosuppression for the treatment of BKVN can increase. Thus the treatment of BKVN has been not well established. Cidofovir is a nucleotide analog against various DNA viruses and was approved for the treatment of cytomegalovirus retinitis in AIDS. The main side effect of cidofovir is nephrotoxicity and it is dose dependent. Several cases have been reported that combination of cidofovir and leflunomide was used for refractory BKVN. However it remains as a dilemma for BKVN treatment because of the nephrotoxicity of cidofovir. Thus we report a case that refractory BKVN to reduction of immunosuppression was successfully treated by combination therapy of low-dose cidofovir and leflunomide in a kidney transplant recipient.
Case report
A 63-year-old male receiving kidney transplant before 6 months was hospitalized due to elevated serum creatinine. He was taking immunosuppressive agents; tacrolimus, mycophenolate mofetil and prednisolone. At 6 months of post transplantation, serum creatinine increased to 2.7 mg/dL. Allograft biopsy was performed and it was compatible with BKVN. BK viral loads (DNA) at admission were 291,250 copies/mL in blood and 195,498,400 copies/mL in urine. Tacrolimus and mycophenolate mofetil were switched to leflunomide (40 mg/day). However, serum creatinine continuously elevated to 4.2 mg/dL with increase of viral loads (546,000 in blood and 785,000,000 copies/mL in urine). Low-dose of cidofovir 0.25 mg/kg was intravenously administered weekly for 4 weeks. At 4 weeks with combination therapy of low-dose of cidofovir and leflunomide, viral load decreased to 4,915 copies/mL in blood and 70,000,000 copies/mL in urine and serum creatinine decreased to 2.2 mg/dL.
Conclusions
Combination therapy of low-dose cidofovir and leflunomide can be considered in a kidney transplant recipient with BKVN.

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