Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (40): 7426-7432.doi: 10.3969/j.issn.2095-4344.2012.40.004

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Anti-virus efficacy of cyclosporine in renal transplant recipients with hepatitis C virus-RNA positive

Liu Tie-shi, Li Xiao-gong, Zhao Xiao-zhi, Liu Guang-xiang, Guo Hong-qian   

  1. Department of Urology, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing Medical University, Nanjing 210008, Jiangsu Province, China
  • Received:2012-07-02 Revised:2012-07-19 Online:2012-09-30 Published:2012-09-30
  • Contact: Guo Hong-qian, Doctor, Doctoral supervisor, Department of Urology, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing Medical University, Nanjing 210008, Jiangsu Province, China dr.ghq@163.com
  • About author:Liu Tie-shi, Attending physician, Department of Urology, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing Medical University, Nanjing 210008, Jiangsu Province, China liutieshi@163.com

Abstract:

BACKGROUND: The selection of immunosuppressants and anti-hepatitis C virus drug is currently the focus for the hepatitis C virus-positive patients after receiving renal transplantation.
OBJECTIVE: To investigate the anti-virus replication effect of cyclosporine in hepatitis C virus-RNA positive renal transplant recipients in addition to its anti-rejection effect.
METHODS: Eleven hepatitis C virus-RNA positive renal transplant recipients were enrolled and treated with cyclosporine, prednisone and mizoribine. Hepatitis C virus-RNA level, hemoglobin, liver functions and renal functions were evaluated before treatment and at 6 and 12 months after treatment.
RESULTS AND CONCLUSION: The median of hepatitis C virus-RNA in 11 patients before treatment, and at 6 and 12 months after treatment were 1.22×107 copies/mL, 1.11×104 copies/mL and 4.19×106 copies/mL respectively. At 6 months after treatment, 8 cases of hepatitis C virus-RNA were negative (hepatitis C virus-RNA < 500 copies/mL), and the total response of hepatitis C virus-RNA was 73%, and the sustained virological response was 55% (6/11) at the final follow-up. There was no significant difference of alanine transaminase, serum creatinine and serum uric acid levels before and after treatment (P > 0.05), and the hemoglobin level was increased after treatment. During the follow-up, acute rejection only occurred in one patient and was controlled within 3 days after methylprednisolone pulse therapy. Cyclosporine-based treatment would be a better choice for renal transplant recipients combined with hepatitis C virus infection for both the anti-virus replication and anti-rejection effect.

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