Randomized Trial of High-Dose Interferon-α-2b Combined With Ribavirin in Patients With Chronic Hepatitis C: Correlation Between Amino Acid Substitutions in the Core/NS5A Region and Virological Response to Interferon Therapy

被引:27
|
作者
Mori, Nami [1 ]
Imamura, Michio [1 ]
Kawakami, Yoshiiku [1 ]
Saneto, Hiromi [1 ]
Kawaoka, Tomokazu [1 ]
Takaki, Shintaro [1 ]
Aikata, Hiroshi [1 ]
Takahashi, Shoichi [1 ]
Chayama, Kazuaki [1 ]
机构
[1] Hiroshima Univ, Dept Med & Mol Sci, Div Frontier Med Sci,Programs Biomed Res, Grad Sch Biomed Sci,Minami Ku, Hiroshima 7348551, Japan
关键词
HCV; interferon; ribavirin; core region; ISDR; SENSITIVITY-DETERMINING REGION; VIRUS GENOTYPE 1B; NONSTRUCTURAL 5A PROTEIN; ALPHA-2B PLUS RIBAVIRIN; NON-B-HEPATITIS; HIGH VIRAL LOAD; COMBINATION THERAPY; CORE PROTEIN; JAPANESE PATIENTS; PEGYLATED INTERFERON-ALPHA-2B;
D O I
10.1002/jmv.21438
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aim of this study was to compare the efficacy of high-dose interferon (IFN)-alpha-2b with standard dose of IFN-alpha-2b in combination with ribavirin (RBV) for patients with chronic hepatitis C virus (HCV) infection, and to investigate the predictive factors associated with virological response. Two hundred Japanese patients with high HCV viral load (>100 KIU/ml) were randomized to 6 or 10 mega units (MU) of 24-week IFN-alpha-2b with RBV. Predictive factors were investigated; including pretreatment amino acid (aa) sequences of the core region and the IFN-sensitive determining region (ISDR). The sustained virological response rate was not different in the two groups (24% vs. 30%) but the incidence of depression was significantly higher in the 10 MU group than 6 MU group (7% vs. 0%, P = 0.02). Younger age (<60) and HCV genotype (2a/b) were significant predictors of sustained virological response. In patients infected with genotype 1b, substitutions of core aa 70 and/or 91, were predictive for non-virological response (P < 0.001), and substitutions in the ISDR was observed frequently in virological responders. Early viral kinetics study showed that serum HCV core antigen decreased more slowly in both patients with aa 70 and/or 91 substitutions in the core and with absence of substitutions in the ISDR. In conclusion, the use of a higher dose of IFN-alpha-2b in combination with RBV did not improve virological response but resulted in higher incidence of depression. Amino acid substitutions in the core and ISDR are predictive of virological response to the therapy in patients with genotype 1b and high viral load. J. Med. Virol. 81:640-649, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:640 / 649
页数:10
相关论文
共 50 条
  • [1] Amino acid substitutions in core and NS5A regions of the HCV genome can predict virological decrease with pegylated interferon plus ribavirin therapy
    Kitamura, Shosuke
    Tsuge, Masataka
    Hatakeyama, Tsuyoshi
    Abe, Hiromi
    Imamura, Michio
    Mori, Nami
    Saneto, Hiromi
    Kawaoka, Tomokazu
    Mitsui, Fukiko
    Hiraga, Nobuhiko
    Takaki, Shintaro
    Kawakami, Yoshiiku
    Aikata, Hiroshi
    Takahashi, Shoichi
    Ohishi, Waka
    Ochi, Hidenori
    Hayes, C. Nelson
    Chayama, Kazuaki
    ANTIVIRAL THERAPY, 2010, 15 (08) : 1087 - 1097
  • [2] Amino acid substitutions in NS5A region of GB virus C and response to interferon therapy
    Kato, T
    Mizokami, M
    Orito, E
    Ohba, K
    Nakano, T
    Kondo, Y
    Tanaka, Y
    Ueda, R
    Mukaide, M
    Yasuda, K
    Iino, S
    JOURNAL OF MEDICAL VIROLOGY, 1999, 57 (04) : 376 - 382
  • [3] Effect of combination therapy with ribavirin and high-dose interferon-α2b for 24 weeks in chronic hepatitis C
    Abe, S
    Narita, R
    Oto, T
    Tabaru, A
    Otsuki, M
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2006, 21 (01) : 308 - 312
  • [4] Mutations in the core and NS5A region of hepatitis C virus genotype 1b and correlation with response to pegylated-interferon-alpha 2b and ribavirin combination therapy
    Hayashi, K.
    Katano, Y.
    Ishigami, M.
    Itoh, A.
    Hirooka, Y.
    Nakano, I.
    Urano, F.
    Yoshioka, K.
    Toyoda, H.
    Kumada, T.
    Goto, H.
    JOURNAL OF VIRAL HEPATITIS, 2011, 18 (04) : 280 - 286
  • [5] High-dose interferon-α2b induction therapy in combination with ribavirin for treatment of chronic hepatitis C in patients with non-response or relapse after interferon-α monotherapy
    Hass, Holger G.
    Kreysel, Christian
    Fischinger, Johannes
    Menzel, Josef
    Kaiser, Stephan
    WORLD JOURNAL OF GASTROENTEROLOGY, 2005, 11 (34) : 5342 - 5346
  • [6] Clinical comparison of high-dose interferon-α2b with or without ribavirin for treatment of interferon-relapsed chronic hepatitis C
    Cheng, PN
    Chow, NH
    Hu, SC
    Young, KC
    Chen, CY
    Jen, CM
    Chang, TT
    DIGESTIVE AND LIVER DISEASE, 2002, 34 (12) : 851 - 856
  • [7] Association of interleukin 28B and mutations in the core and NS5A region of hepatitis C virus with response to peg-interferon and ribavirin therapy
    Hayashi, Kazuhiko
    Katano, Yoshiaki
    Honda, Takashi
    Ishigami, Masatoshi
    Itoh, Akihiro
    Hirooka, Yoshiki
    Ishikawa, Tetsuya
    Nakano, Isao
    Yoshioka, Kentaro
    Toyoda, Hidenori
    Kumada, Takashi
    Goto, Hidemi
    LIVER INTERNATIONAL, 2011, 31 (09) : 1359 - 1365
  • [8] High-dose interferon-α2b induction therapy in combination with ribavirin for treatment of chronic hepatitis C in patients with non-response or relapse after interferon-a monotherapy
    Holger G. Hass
    Christian Kreysel
    Johannes Fischinger
    Josef Menzel
    Stephan Kaiser
    World Journal of Gastroenterology, 2005, (34) : 5342 - 5346
  • [9] High-dose interferon-α2b plus ribavirin for retreatment of interferon-nonresponsive patients infected with genotype 1 hepatitis C virus
    Buti, M
    Morral, S
    Sanchez, F
    Martell, M
    Stalgis, C
    Esteban, R
    DIGESTIVE DISEASES AND SCIENCES, 2001, 46 (11) : 2396 - 2400
  • [10] Secondary Structure of the Amino-Terminal Region of HCV NS3 and Virological Response to Pegylated Interferon Plus Ribavirin Therapy for Chronic Hepatitis C
    Sanjo, Mai
    Saito, Takafumi
    Ishii, Rika
    Nishise, Yuko
    Haga, Hiroaki
    Okumoto, Kazuo
    Ito, Junitsu
    Watanabe, Hisayoshi
    Saito, Koji
    Togashi, Hitoshi
    Fukuda, Kazuto
    Imai, Yasuharu
    El-Shamy, Ahmed
    Deng, Lin
    Shoji, Ikuo
    Hotta, Hak
    Kawata, Sumio
    JOURNAL OF MEDICAL VIROLOGY, 2010, 82 (08) : 1364 - 1370