Viral and host factors in the prediction of response to interferon-α therapy in chronic hepatitis C after long-term follow-up

被引:35
作者
Knolle, PA
Kremp, S
Hohler, T
Krummenauer, F
Schirmacher, P
Gerken, G
机构
[1] Univ Mainz, Dept Med 1, D-6500 Mainz, Germany
[2] Univ Mainz, Dept Med Stat & Documentat, D-6500 Mainz, Germany
[3] Univ Mainz, Dept Pathol, D-6500 Mainz, Germany
关键词
hepatitis C virus; interferon treatment; long-term outcome; viral hepatitis;
D O I
10.1046/j.1365-2893.1998.00127.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Acute infection with hepatitis C virus (HCV) develops into a chronic hepatitis in about 50-70% of patients. Treatment of these patients with interferon-alpha (IFN-alpha) results in a sustained long-term response in only 15-20% but causes numerous unwanted side-effects in a higher percentage of patients. The aim of our study was to define host or viral parameters that would allow identification of responders and non-responders to IFN-alpha prior to the onset of treatment. We studied a group of 87 patients suffering from chronic hepatitis C who were treated with IFN-alpha. After long-term follow-up, 18: patients (21%) showed a sustained response to IFN-alpha therapy (normalization of serum transaminases and loss of viral RNA from serum) for up to 7 years after therapy had ceased. By univariate and multivariate analyses, no; host factors were found to be predictive of response to. therapy. Neither the degree of inflammation or fibrosis in liver biopsy samples obtained before treatment nor immunogenetic factors (major histocompatibility complex II haplotype and tumour necrosis factor-alpha promoter polymorphism) were associated with response to therapy. In contrast, viral parameters showed a strong association with response to therapy. HCV genotype 3 was found significantly more frequently in responders (P = 0.034), and mean HCV RNA concentration was lower in responders (3.1 x 10(4)) than in non-responders (2.5 x 10(5)) (P = 0.01). By multivariate analysis, both HCV genotype and HCV RNA concentration were independent predictors of response to therapy. However, exact prediction of response to treatment for an individual patient was not possible on the basis of pretreatment viral RNA concentration or viral genotype. The best association with response to therapy was found to be clearance of HCV RNA from serum 3 months after the start of treatment (32 of 34 partial and sustained responders vs 0 of 53 non-responders; P = 0.001). In conclusion, determination of pretreatment; viral factors, but not host factors, was significantly correlated with treatment response but did not give an accurate prediction for patients, whereas clearance of HCV RNA from serum after 3 months of therapy was predictive of response to therapy.
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收藏
页码:399 / 406
页数:8
相关论文
共 32 条
[1]   Permanent response to alpha-interferon therapy in chronic hepatitis C is preceded by rapid clearance of HCV-RNA from serum [J].
Ampurdanes, S ;
Olmedo, E ;
Maluenda, MD ;
Forns, X ;
LopezLabrador, FX ;
Costa, J ;
SanchezTapias, JM ;
deAnta, MTJ ;
Rodes, J .
JOURNAL OF HEPATOLOGY, 1996, 25 (06) :827-832
[2]   RAPID HLA-DRB1 GENOTYPING BY NESTED PCR-AMPLIFICATION [J].
BEIN, G ;
GLASER, R ;
KIRCHNER, H .
TISSUE ANTIGENS, 1992, 39 (02) :68-73
[3]  
Breslow NE, 1980, IARC SCI PUBL, VI, P5
[4]  
Brinkman B M, 1995, J Inflamm, V46, P32
[5]   Pretreatment virus load and multiple amino acid substitutions in the interferon sensitivity-determining region predict the outcome of interferon treatment in patients with chronic genotype 1b hepatitis C virus infection [J].
Chayama, K ;
Tsubota, A ;
Kobayashi, M ;
Okamoto, K ;
Hashimoto, M ;
Miyano, Y ;
Koike, H ;
Kobayashi, M ;
Koida, I ;
Arase, Y ;
Saitoh, S ;
Suzuki, Y ;
Murashima, N ;
Ikeda, K ;
Kumada, H .
HEPATOLOGY, 1997, 25 (03) :745-749
[6]  
CHEVALLIER M, 1994, HEPATOLOGY, V20, P349, DOI 10.1002/hep.1840200213
[7]  
DESMET VJ, 1994, HEPATOLOGY, V19, P1513, DOI 10.1002/hep.1840190629
[8]   FLUCTUATION OF HEPATITIS-C VIRUS QUASI-SPECIES IN PERSISTENT INFECTION AND INTERFERON TREATMENT REVEALED BY SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS [J].
ENOMOTO, N ;
KUROSAKI, M ;
TANAKA, Y ;
MARUMO, F ;
SATO, C .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :1361-1369
[9]   Mutations in the nonstructural protein 5A gene and response to interferon in patients with chronic hepatitis C virus 1b infection [J].
Enomoto, N ;
Sakuma, I ;
Asahina, Y ;
Kurosaki, M ;
Murakami, T ;
Yamamoto, C ;
Ogura, Y ;
Izumi, N ;
Marumo, F ;
Sato, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (02) :77-81
[10]   COMPARISON OF FULL-LENGTH SEQUENCES OF INTERFERON-SENSITIVE AND RESISTANT HEPATITIS-C VIRUS 1B - SENSITIVITY TO INTERFERON IS CONFERRED BY AMINO-ACID SUBSTITUTIONS IN THE NS5A REGION [J].
ENOMOTO, N ;
SAKUMA, I ;
ASAHINA, Y ;
KUROSAKI, M ;
MURAKAMI, T ;
YAMAMOTO, C ;
IZUMI, N ;
MARUMO, F ;
SATO, C .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (01) :224-230