Impact of Hepatitis B Virus Integration Into Liver Tissue on the Efficacy of Peginterferon and Ribavirin Therapy in Hepatitis B Virus-negative Chronic Hepatitis C Patients

被引:2
作者
Toyoda, Hidenori [1 ]
Kumada, Takashi [1 ]
Tada, Toshifumi [1 ]
Murakami, Yoshiki [2 ]
机构
[1] Ogaki Municipal Hosp, Dept Gastroenterol, Ogaki, Gifu 5038502, Japan
[2] Kyoto Univ, Ctr Genom Med, Grad Sch Med, Kyoto, Japan
关键词
chronic hepatitis C; early virologic response; hepatitis B virus integration; peginterferon and ribavirin combination therapy; rapid virologic response; sustained virologic response; GENOME-WIDE ASSOCIATION; HEPATOCELLULAR-CARCINOMA; DNA INTEGRATION; GENETIC-VARIATION; INTERFERON-ALPHA; HBV DNA; HCV; IL28B; CLEARANCE; INFECTION;
D O I
10.1097/MCG.0b013e31829c409d
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background:Integration of hepatitis B virus (HBV) DNA into host hepatic DNA is found in patients without HBV surface antigen (HBsAg). We investigated the prevalence of HBV integration and its association with the outcome of peginterferon (PEG-IFN) and ribavirin combination therapy in HBsAg-negative chronic hepatitis C patients.Study:We analyzed 157 patients chronically infected with hepatitis C virus (HCV) with viral load 5.0 log(10) IU/mL, who underwent PEG-IFN and ribavirin combination therapy. HBV integration was measured by an Alu-PCR assay with liver specimens obtained by needle biopsy before treatment.Results:HBV integration was identified in 54 of the 157 (34.4%) patients. There were no significant differences between patients with and without HBV integration with regard to baseline characteristics including liver histology, pretreatment HCV RNA levels, and genetic polymorphisms near the IL28B gene. In patients with HCV genotype 1b (n=91), a more favorable viral response was observed in patients with HBV integration during therapy, with higher rates of rapid and complete early virologic response. The rate of sustained virologic response (SVR) was significantly higher in patients with HBV integration than those without (P=0.0098). Multivariate analysis identified HBV integration and IL28B polymorphisms as independent factors associated with SVR.Conclusions:HBV integration was associated with favorable viral responses and a higher SVR rate to combination therapy with PEG-IFN and ribavirin in patients infected with HCV genotype 1b. Further studies will be required to confirm this association and elucidate its underlying mechanisms.
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页码:73 / 79
页数:7
相关论文
共 29 条
[1]   Molecular bases for the development of hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) [J].
Bréchot, C ;
Gozuacik, D ;
Murakami, Y ;
Paterlini-Bréchot, P .
SEMINARS IN CANCER BIOLOGY, 2000, 10 (03) :211-231
[2]   Occult hepatitis B virus infection in patients with chronic hepatitis C liver disease [J].
Cacciola, I ;
Pollicino, T ;
Squadrito, G ;
Cerenzia, G ;
Orlando, ME ;
Raimondo, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (01) :22-26
[3]   Improved COBAS TaqMan hepatitis C virus test (version 2.0) for use with the high pure system: Enhanced genotype inclusivity and performance characteristics in a multisite study [J].
Colucci, G. ;
Ferguson, J. ;
Harkleroad, C. ;
Lee, S. ;
Romo, D. ;
Soviero, S. ;
Thompson, J. ;
Velez, M. ;
Wang, A. ;
Miyahara, Y. ;
Young, S. ;
Sarrazin, C. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (11) :3595-3600
[4]   HEPATITIS-B VIRUS-DNA INTEGRATION IN A SEQUENCE HOMOLOGOUS TO V-ERB-A AND STEROID-RECEPTOR GENES IN A HEPATOCELLULAR-CARCINOMA [J].
DEJEAN, A ;
BOUGUELERET, L ;
GRZESCHIK, KH ;
TIOLLAIS, P .
NATURE, 1986, 322 (6074) :70-73
[5]   Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance [J].
Ge, Dongliang ;
Fellay, Jacques ;
Thompson, Alexander J. ;
Simon, Jason S. ;
Shianna, Kevin V. ;
Urban, Thomas J. ;
Heinzen, Erin L. ;
Qiu, Ping ;
Bertelsen, Arthur H. ;
Muir, Andrew J. ;
Sulkowski, Mark ;
McHutchison, John G. ;
Goldstein, David B. .
NATURE, 2009, 461 (7262) :399-401
[6]   Diagnosis, Management, and Treatment of Hepatitis C: An Update [J].
Ghany, Marc G. ;
Strader, Doris B. ;
Thomas, David L. ;
Seeff, Leonard B. .
HEPATOLOGY, 2009, 49 (04) :1335-1374
[7]   State of HBV DNA in HBsAg-negative, anti-HCV-positive hepatocellular carcinoma: Existence of HBV DNA possibly as nonintegrated form with analysis by Alu-HBV DNA PCR and conventional HBVPCR [J].
Kawai, S ;
Yokosuka, O ;
Imazeki, F ;
Maru, Y ;
Saisho, H .
JOURNAL OF MEDICAL VIROLOGY, 2001, 64 (04) :410-418
[8]   Replicated Association Between an IL28B Gene Variant and a Sustained Response to Pegylated Interferon and Ribavirin [J].
McCarthy, Jeanette J. ;
Li, Josephine H. ;
Thompson, Alexander ;
Suchindran, Sunil ;
Lao, Xiang Qian ;
Patel, Keyur ;
Tillmann, Hans L. ;
Muir, Andrew J. ;
McHutchison, John G. .
GASTROENTEROLOGY, 2010, 138 (07) :2307-2314
[9]   NOVEL PCR TECHNIQUE USING ALU-SPECIFIC PRIMERS TO IDENTIFY UNKNOWN FLANKING SEQUENCES FROM THE HUMAN GENOME [J].
MINAMI, M ;
POUSSIN, K ;
BRECHOT, C ;
PATERLINI, P .
GENOMICS, 1995, 29 (02) :403-408
[10]   Large scaled analysis of hepatitis B virus (HBV) DNA integration in HBV related hepatocellular carcinomas [J].
Murakami, Y ;
Saigo, K ;
Takashima, H ;
Minami, M ;
Okanoue, T ;
Bréchot, C ;
Paterlini-Bréchot, P .
GUT, 2005, 54 (08) :1162-1168