Long-term results of treatment of chronic hepatitis B, C and D with interferon-alpha in renal allograft recipients

• Published in: Transplant international 1998, Vol.11 Suppl 1, p.S135-S139
• Main Authors: Durlik, M, Gaciong, Z, Rowińska, D, Rancewicz, Z, Lewandowska, D, Kozłowska, B, Wyzgał, J, Soluch, L, Walewska-Zielecka, B, Rowiński, W, Lao, M
• Format: Article
• Language: English
• Subjects: Adult; Female; Hepatitis B, Chronic - drug therapy; Hepatitis C, Chronic - drug therapy; Hepatitis D, Chronic - drug therapy; Humans; Interferon-alpha - therapeutic use; Kidney Transplantation; Male; Middle Aged; Postoperative Complications - drug therapy
• ISSN: 0934-0874; 1432-2277
• DOI: 10.1007/s001470050445

The aim of this study was to evaluate the efficacy and safety of interferon-alpha (IFN-alpha) therapy of chronic hepatitis B, C and D (HBV, HCV and HDV, respectively) in renal transplant recipients. A group of 42 patients (30 males, 12 females, mean age 38 years) with documented viraemia and chronic active hepatitis (CAH) were studied, of whom 1 had HBV infection alone, 11 had HCV infection alone, 3 had HBV and HDV infection concomitantly, 12 had HBV and HCV infection concomitantly, and 2 had HBV, HCV and HDV infection concomitantly. Patients received 3 MU IFN-alpha three times weekly for 6 months. After IFN-alpha therapy, 18 patients (43%) achieved normal alanine aminotransferase (ALT) activity and a partial response was observed in 12 (29%) patients. Two patients relapsed (one with HCV and one with HBV + HCV infection) immediately after the cessation of IFN-alpha therapy. Repeated liver biopsy was performed in 16 patients after 6-24 months of therapy and revealed progression to cirrhosis in five patients, remission in two and stable disease in nine. None of the patients cleared HCV RNA, four patients cleared HBeAg (two also HDV), and one both HBV and HCV. Five patients died during IFN-alpha therapy (one as a consequence of liver failure), and four died during the 6 months after therapy (two as a consequence of liver failure). During IFN-alpha therapy renal allograft function remained stable in 31 patients and acute rejection episodes occurred in 7, of whom 5 lost their graft and all had experienced rejection episodes before. In 16 patients normalization of ALT continued during long-term follow-up (median 22 months, range 0-84 months). IFN-alpha seemed to be moderately effective in the treatment of chronic HBV or HCV infections, but cannot be recommended for recipients infected with both HBV and HCV.