Virological response to interferon therapy of chronic hepatitis B as measured by a highly sensitive assay

被引:10
作者
Lindh, M
Hannoun, C
Horal, P
Krogsgaard, K
机构
[1] Gothenburg Univ, Dept Clin Virol, S-41346 Gothenburg, Sweden
[2] Hvidovre Univ Hosp, Clin Res Unit, Copenhagen, Denmark
关键词
hepatitis B virus; quantification; response; steroid; therapy;
D O I
10.1046/j.1365-2893.2001.00306.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In the interferon (IFN) treatment of chronic hepatitis B, there is no accepted definition of virological response as measured by highly sensitive HBV DNA assays. In the present study of 98 patients given IFN (10 MU/day for 1 week, then 10 MU TIW for 11 weeks) with or without prednisolone priming, a virological response was identified as log HBV DNA/mL below 6.0 (by Amplicor Monitor, Roche) 6 months post-treatment. At this time, 92% (33/36) of the sustained responders (SR) still had detectable viraemia with log HBV DNA/mL at 4.30 +/- 0.15 ( SEM), as compared with 8.69 +/- 0.097 in nonsustained responders. Pretreatment viraemia below a threshold at 500 million copies/mL was associated with higher chance of response (P = 0.023). Prednisolone enhanced the sustained response (53% vs. 30%, P = 0.025), and in particular end-of-treatment response (ETR, 50% vs. 10%, P < 0.0001). ETR was predictive for SR (P < 0.0001), especially when log HBV DNA/mL was < 4.0 (PPV = 92%). The potential value of differentiating the therapy of chronic hepatitis B on the basis of viraemia levels, as measured by highly sensitive assays, should be further investigated.
引用
收藏
页码:349 / 357
页数:9
相关论文
共 51 条
[1]   WHICH PATIENTS WITH CHRONIC HEPATITIS-B VIRUS-INFECTION WILL RESPOND TO ALPHA-INTERFERON THERAPY - A STATISTICAL-ANALYSIS OF PREDICTIVE FACTORS [J].
BROOK, MG ;
KARAYIANNIS, P ;
THOMAS, HC .
HEPATOLOGY, 1989, 10 (05) :761-763
[2]   Effects of a naturally occurring mutation in the hepatitis B virus basal core promoter on precore gene expression and viral replication [J].
Buckwold, VE ;
Xu, ZC ;
Chen, M ;
Yen, TSB ;
Ou, JH .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5845-5851
[3]   Comparison of four methods for quantitative measurement of hepatitis B viral DNA [J].
Butterworth, LA ;
Prior, SL ;
Buda, PJ ;
Faoagali, JL ;
Cooksley, WGE .
JOURNAL OF HEPATOLOGY, 1996, 24 (06) :686-691
[4]  
CARMAN WF, 1989, LANCET, V2, P588
[5]   INCIDENCE OF HEPATITIS-B VIREMIA, DETECTED USING THE POLYMERASE CHAIN-REACTION, AFTER SUCCESSFUL THERAPY OF HEPATITIS-B VIRUS CARRIERS WITH INTERFERON-ALPHA [J].
CARMAN, WF ;
DOURAKIS, S ;
KARAYIANNIS, P ;
CROSSEY, M ;
DROBNER, R ;
THOMAS, HC .
JOURNAL OF MEDICAL VIROLOGY, 1991, 34 (02) :114-118
[6]   HEPATITIS-B VIRUS IMMUNOPATHOGENESIS [J].
CHISARI, FV ;
FERRARI, C .
ANNUAL REVIEW OF IMMUNOLOGY, 1995, 13 :29-60
[7]   GLUCOCORTICOID STIMULATES HEPATITIS-B VIRAL GENE-EXPRESSION IN CULTURED HUMAN HEPATOMA-CELLS [J].
CHOU, CK ;
WANG, LH ;
LIN, HM ;
CHI, CW .
HEPATOLOGY, 1992, 16 (01) :13-18
[8]  
CHU CHM, 1985, LIVER, V5, P117
[9]   REEVALUATION OF ALPHA-INTERFERON TREATMENT OF CHRONIC HEPATITIS-B USING POLYMERASE CHAIN-REACTION [J].
CHUNG, HT ;
LOK, ASF ;
LAI, CL .
JOURNAL OF HEPATOLOGY, 1993, 17 (02) :208-214
[10]   PREDNISONE-INTERFERON COMBINATION IN THE TREATMENT OF CHRONIC HEPATITIS-B - DIRECT AND INDIRECT METANALYSIS [J].
COHARD, M ;
POYNARD, T ;
MATHURIN, P ;
ZARSKI, JP .
HEPATOLOGY, 1994, 20 (06) :1390-1398