Association of Lamivudine-Resistant Mutational Patterns With the Antiviral Effect of Adefovir in Patients With Chronic Hepatitis B

被引:15
作者
Cha, Choong Keun [2 ]
Kwon, Hyeok Choon [1 ]
Cheong, Jae Youn [1 ]
Cho, Sung Won [1 ]
Hong, Sun Pyo [3 ]
Kim, Soo-Ok [3 ]
Yoo, Wang Don [3 ]
机构
[1] Ajou Univ, Sch Med, Dept Gastroenterol, Suwon 442721, South Korea
[2] Pochon CHA Univ Coll Med, CHA Biomed Ctr, Seoul, South Korea
[3] GeneMatrix Inc, Yongin, South Korea
关键词
hepatitis B virus; mutation; reverse transcriptase; antiviral resistance; REPLICATION IN-VITRO; VIRUS POLYMERASE; RESCUE THERAPY; DIPIVOXIL; SEQUENCES; DNA; EMERGENCE; VARIANTS; MUTANTS; SAFETY;
D O I
10.1002/jmv.21402
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Adefovir has a potent antiviral activity as a rescue treatment against lamivudine-resistant strains. The aim of this study was to assess the patterns of lamivudine-resistant mutations and their influence on the virologic response to adefovir rescue therapy in patients with lamivudine-resistant chronic hepatitis B. Sixty-seven patients with lamivudine-resistant chronic hepatitis B were treated with adefovir monotherapy. Baseline blood samples were analyzed for lamivudine-resistant mutations via restriction fragment mass polymorphism. Virologic responses, ALT normalization and loss of HBeAg were assessed. Serum HBV DNA levels were measured using real-time PCR at baseline and 24 weeks of adefovir therapy. Of the 67 patients with chronic hepatitis B, 65 patients (97%) had lamivudine-resistant mutations in the YMDD motif [27 (41%) rtM2041, 22 (34%) rtM204V, and 16 (25%) rtM2041/V]. In addition to the YMDD mutations, the rtL180M, rtL801, and rtV173L mutations were also present in 78%, 43%, and 11% of patients, respectively. The rtM204V mutation always accompanied rtL180M, and rtL801 was always observed in conjunction with rtM2041. Decrease in mean serum HBV did not differ between patients carrying the rtM2041 versus rtM204V mutant at week 24 (-3.3 vs. -3.3 log 10 copies/ml, respectively; P = 0.303). The presence of the rtL180M, rtL801, and rtV173L did not significantly affect viral load reduction during adefovir administration. These results demonstrate that the rtL801 mutant is co-selected with rtM2041 as a compensatory mutation in the same manner as rtL180M with rtM204V, and that adefovir shows similar antiviral efficacy against all of the evaluated patterns of lamivudine-resistant HBV mutations. J. Med. Virol. 81:417-424, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:417 / 424
页数:8
相关论文
共 32 条
  • [1] Identification and characterization of mutations in hepatitis B virus resistant to lamivudine
    Allen, MI
    Deslauriers, M
    Andrews, CW
    Tipples, GA
    Walters, KA
    Tyrrell, DLJ
    Brown, N
    Condreay, LD
    [J]. HEPATOLOGY, 1998, 27 (06) : 1670 - 1677
  • [2] [Anonymous], 2003, J Hepatol, V39 Suppl 1, pS1
  • [3] Hepatitis B virus genotypes: comparison of genotyping methods
    Bartholomeusz, A
    Schaefer, S
    [J]. REVIEWS IN MEDICAL VIROLOGY, 2004, 14 (01) : 3 - 16
  • [4] Safety and efficacy of adefovir dipivoxil in patients co-infected with HIV-1 and lamivudine-resistant hepatitis B virus: an open-label pilot study
    Benhamou, Y
    Bochet, M
    Thibault, V
    Calvez, V
    Fievet, MH
    Vig, P
    Gibbs, CS
    Brosgart, C
    Fry, J
    Namini, H
    Katiama, C
    Poynard, T
    [J]. LANCET, 2001, 358 (9283) : 718 - 723
  • [5] Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level
    Chen, CJ
    Yang, HI
    Su, J
    Jen, CL
    You, SL
    Lu, SN
    Huang, GT
    Iloeje, UH
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (01): : 65 - 73
  • [6] Management of chronic hepatitis B
    Conjeevaram, HS
    Lok, ASF
    [J]. JOURNAL OF HEPATOLOGY, 2003, 38 : S90 - S103
  • [7] The hepatitis B virus polymerase mutation rtV173L is selected during lamivudine therapy and enhances viral replication in vitro
    Delaney, WE
    Yang, HL
    Westland, CE
    Das, K
    Arnold, E
    Gibbs, CS
    Miller, MD
    Xiong, S
    [J]. JOURNAL OF VIROLOGY, 2003, 77 (21) : 11833 - 11841
  • [8] Delaney WE, 2001, ANTIVIR CHEM CHEMOTH, V12, P1
  • [9] Lamivudine as initial treatment for chronic hepatitis B in the United States
    Dienstag, JL
    Schiff, ER
    Wright, TL
    Perrillo, RP
    Hann, HWL
    Goodman, Z
    Crowther, L
    Condreay, LD
    Woessner, M
    Rubin, M
    Brown, NA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (17) : 1256 - 1263
  • [10] Mutational patterns of hepatitis B virus genome and clinical outcomes after emergence of drug-resistant variants during lamivudine therapy: Analyses of the polymerase gene and full-length sequences
    Enomoto, Masaru
    Tamori, Akihiro
    Kohmoto, Madoka Toyama
    Morikawa, Hiroyasu
    Habu, Daiki
    Sakaguchi, Hiroki
    Takeda, Tadashi
    Seki, Shuichi
    Kawada, Norifumi
    Shiomi, Susumu
    Nishiguchi, Shuhei
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2007, 79 (11) : 1664 - 1670