Mycophenolate mofetil in combination with recombinant interferon alfa-2a in interferon-nonresponder patients with chronic hepatitis C

被引:25
作者
Cornberg, M
Hinrichsen, H
Teuber, G
Berg, T
Naumann, U
Falkenberg, C
Zeuzem, S
Manns, MP
机构
[1] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, D-30625 Hannover, Germany
[2] Univ Kiel, Med Klin 1, D-2300 Kiel, Germany
[3] Univ Frankfurt Klinikum, Med Klin 2, D-6000 Frankfurt, Germany
[4] Humboldt Univ, Charite, Med Klin S Hepatol & Gastroenterol, Berlin, Germany
关键词
hepatitis C virus; chronic hepatitis C; interferon alfa-2a; ribavirin; mycophenolate mofetil; therapy;
D O I
10.1016/S0168-8278(02)00300-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Since ribavirin was able to improve the antiviral efficacy of interferon alfa in patients with chronic hepatitis C, several other adjuncts have been studied. It has been shown that mycophenolate mofetil (MMF) is a more potent inhibitor of the inosine 5'-monophosphate-dehydrogenase (IMPDH) than ribavirin. The present study is a pilot study evaluating the efficacy and safety of combination therapy with interferon alfa-2a and MMF in interferon alfa nonresponder patients. Methods: Thirty-eight adult patients with chronic hepatitis C who did not respond to a previous interferon alfa monotherapy were enrolled to receive 6 million units of interferon alfa-2a tiw in combination with MMF (1 week 500 mg/day, 1 week 1000 mg/day, 22 weeks 2000 mg/day). Results: An interim analysis of 29 patients after 12 weeks of therapy showed that only one patient had negative hepatitis C virus-RNA at this time point. There was no significant reduction of the viral load during therapy. Due to inefficacy the study was discontinued. Conclusions: Combination therapy of interferon alfa-2a and MMF is ineffective in improving virological response rates in nonresponder patients with chronic hepatitis C. These data suggest that inhibition of the IMPDH seems not to be the major mechanism of ribavirin in enhancing the antiviral effect of interferon alfa in chronic hepatitis C. (C) 2002 European Association for the Study of the Liver. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:843 / 847
页数:5
相关论文
共 26 条
[1]  
Afdhal N, 2001, HEPATOLOGY, V34, p243A
[2]  
Allison AC, 1996, CLIN TRANSPLANT, V10, P77
[3]   Mycophenolate mofetil and its mechanisms of action [J].
Allison, AC ;
Eugui, EM .
IMMUNOPHARMACOLOGY, 2000, 47 (2-3) :85-118
[4]  
Chapman WC, 1999, HEPATOLOGY, V30, p175A
[5]  
Ferenci P, 2001, HEPATOLOGY, V34, p351A
[6]   Mycophenolic acid, an immunosuppressive agent, inhibits HBV replication in vitro [J].
Gong, ZJ ;
De Meyer, S ;
Clarysse, C ;
Verslype, C ;
Neyts, J ;
De Clercq, E ;
Yap, SH .
JOURNAL OF VIRAL HEPATITIS, 1999, 6 (03) :229-236
[7]   POLYMERASE SUBSTRATE DEPLETION - A NOVEL STRATEGY FOR INHIBITING THE REPLICATION OF THE HUMAN-IMMUNODEFICIENCY-VIRUS [J].
ICHIMURA, H ;
LEVY, JA .
VIROLOGY, 1995, 211 (02) :554-560
[8]  
Jain J, 2001, J PHARM SCI-US, V90, P625, DOI 10.1002/1520-6017(200105)90:5<625::AID-JPS1019>3.0.CO
[9]  
2-1
[10]   Mycophenolate mofetil [J].
Lipsky, JJ .
LANCET, 1996, 348 (9038) :1357-1359