Spontaneous viral clearance in patients with acute hepatitis C can be predicted by repeated measurements of serum viral load

被引:179
作者
Hofer, H
Watkins-Riedel, T
Janata, O
Penner, E
Holzmann, H
Steindl-Munda, P
Gangl, A
Ferenci, P
机构
[1] Univ Vienna, Dept Internal Med Gastroenterol & Hepatol 4, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Clin Virol, A-1090 Vienna, Austria
[3] SMZ Ost, Vienna, Austria
关键词
D O I
10.1053/jhep.2003.50019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Early interferon (IFN) therapy prevents viral persistence in acute hepatitis C, but in view of the resulting costs and morbidity patients who really need therapy have to be identified. Twelve consecutive patients with acute hepatitis C (9 women, 3 men, mean age: 39.5 +/- 18.8 y, genotype 1: 7, genotype 3a: 3, 2 could not be genotyped) were studied. The sources of infection were medical procedures in 6, sexual transmission in 3, and intravenous drug abuse in 3 patients. Viral load was measured by Cobas Amplicor HCV Monitor v2.0 (Roche Diagnostic Systems, Branchburg, NY). The time from infection to clinical symptoms was 43.3 +/- 8.6 (mean +/- SD) days. Eight patients cleared hepatitis C virus (HCV) spontaneously and remained HCV-RNA negative with a follow-up of 9.0 +/- 3.9 months. In these patients viral load declined fast and continuously. The time from exposure to HCV-RNA negativity was 77.4 +/- 25.3 and from the first symptoms was 34.7 +/- 22.1 days. In 4 patients HCV-RNA levels remained high or even increased. Two of them became sustained responders to treatment initiated after a 6-week observation period. The 2 remaining patients were not treated (one because of contraindications for IFN, the other declined therapy) and are still HCV-RNA positive. In conclusion, patients with acute icteric hepatitis C have a high rate of spontaneous viral clearance within the first month after the onset of symptoms. IFN therapy appears only needed in patients who fail to dear the virus within 35 days after onset of symptoms. By this approach, IFN therapy was not necessary in two thirds of patients with acute hepatitis C.
引用
收藏
页码:60 / 64
页数:5
相关论文
共 38 条
[1]  
ALBERTI A, 1994, VIRAL HEPATITIS LIVE, P604
[2]  
[Anonymous], 1999, J Hepatol, V30, P956
[3]  
Calleri G, 1998, ITAL J GASTROENTEROL, V30, P181
[4]   Pathogenesis of chronic hepatitis C: Immunological features of hepatic injury and viral persistence [J].
Cerny, A ;
Chisari, FV .
HEPATOLOGY, 1999, 30 (03) :595-601
[5]  
Delwaide J, 1999, HEPATOLOGY, V30, p264A
[6]   Combination of interferon induction therapy and ribavirin in chronic hepatitis C [J].
Ferenci, P ;
Brunner, H ;
Nachbaur, K ;
Datz, C ;
Gschwantler, M ;
Hofer, H ;
Stauber, R ;
Hackl, F ;
Jessner, W ;
Rosenbeiger, M ;
Munda-Steindl, P ;
Hegenbarth, K ;
Gangl, A ;
Vogel, W .
HEPATOLOGY, 2001, 34 (05) :1006-1011
[7]   Treatment of patients with chronic hepatitis C not responding to interferon with high-dose interferon alpha with or without ribavirin:: final results of a prospective randomized trial [J].
Ferenci, P ;
Stauber, R ;
Steindl-Munda, P ;
Gschwantler, M ;
Fickert, P ;
Datz, C ;
Müller, C ;
Hackl, F ;
Rainer, W ;
Watkins-Riedel, T ;
Lin, W ;
Krejs, GJ ;
Gangl, A .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2001, 13 (06) :699-705
[8]   Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. [J].
Fried, MW ;
Shiffman, ML ;
Reddy, KR ;
Smith, C ;
Marinos, G ;
Goncales, FL ;
Haussinger, D ;
Diago, M ;
Carosi, G ;
Dhumeaux, D ;
Craxi, A ;
Lin, A ;
Hoffman, J ;
Yu, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (13) :975-982
[9]  
Gerlach TJ, 2001, HEPATOLOGY, V34, p341A
[10]   HEPATITIS-C VIRUS VIREMIA FOLLOWING CLINICAL RESOLUTION OF ACUTE HEPATITIS-C [J].
GIUBERTI, T ;
MARIN, MG ;
FERRARI, C ;
MARCHELLI, S ;
SCHIANCHI, C ;
ANTONI, AMD ;
PIZZOCOLO, G ;
FIACCADORI, F .
JOURNAL OF HEPATOLOGY, 1994, 20 (05) :666-671