Inhibition of hepatitis B virus by D-fraction from Grifola frondosa:: Synergistic effect of combination with interferon-α in HepG2 2.2.15

被引:44
作者
Gu, Chang-Qing [1 ]
Li, Jun-Wen [1 ]
Chao, Fu-Huan [1 ]
机构
[1] Inst Hlth & Environm Med, Tianjin 300050, Peoples R China
关键词
antiviral; Grifola frondosa; interferon; hepatitis B virus; combination;
D O I
10.1016/j.antiviral.2006.05.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, D-fraction extracted from Grifola frondosa (GF-D) and its combination with human interferon alpha-2b (IFN) were investigated for the inhibitory effect on hepatitis B virus (HBV) in HepG2 2.2.15 cells (2.2.15 cells). HBV DNA and viral antigens were analyzed by a quantitative real-time polymerase chain reaction and end-point titration in radioimmunoassays, respectively. The results showed that GF-D or IFN alone could inhibit HBV DNA in 2.2.15 cells with the 50% inhibitory concentration (IC50) of 0.59 mg/ml and 1399 IU/ml, respectively. We further investigated the combination of GF-D and IFN for anti-HBV activity and found that they synergistically inhibited HBV replication in 2.2.15 cells. In combination with 0.45 mg/ml GF-D, the apparent IC50 value for IFN was 154 IU/ml. This 9-fold increase in antiviral activity of IFN suggested that GF-D could synergize with IFN. These results indicate that GF-D, in combination with IFN, might provide a potentially effective therapy against chronic HBV infections. (c) 2006 Published by Elsevier B.V.
引用
收藏
页码:162 / 165
页数:4
相关论文
共 22 条
  • [1] AOKI M, 1993, BIOSCI BIOTECH BIOCH, V57, P178
  • [2] In vitro inhibition of Chikungunya and Semliki Forest viruses replication by antiviral compounds:: synergistic effect of interferon-α and ribavirin combination
    Briolant, S
    Garin, D
    Scaramozzino, N
    Jouan, A
    Crance, JM
    [J]. ANTIVIRAL RESEARCH, 2004, 61 (02) : 111 - 117
  • [3] New therapeutic approaches to the alphaherpesvirus infections
    Cassady, KA
    Whitley, RJ
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 (02) : 119 - 128
  • [4] Chen N, 2004, PROG BIOCHEM BIOPHYS, V31, P283
  • [5] Real-time PCR for detection and quantitation of hepatitis B virus DNA
    Chen, RW
    Piiparinen, H
    Seppänen, M
    Koskela, P
    Sarna, S
    Lappalainen, M
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2001, 65 (02) : 250 - 256
  • [6] DNA polymerase activity of hepatitis B virus particles: Differential inhibition by L-enantiomers of nucleotide analogs
    Davis, MG
    Wilson, JE
    VanDraanen, NA
    Miller, WH
    Freeman, GA
    Daluge, SM
    Boyd, FL
    Aulabaugh, AE
    Painter, GR
    Boone, LR
    [J]. ANTIVIRAL RESEARCH, 1996, 30 (2-3) : 133 - 145
  • [7] Kinetic analysis of wild-type and YMDD mutant hepatitis B virus polymerases and effects of deoxyribonucleotide concentrations on polymerase activity
    Gaillard, RK
    Barnard, J
    Lopez, V
    Hodges, P
    Bourne, E
    Johnson, L
    Allen, MI
    Condreay, P
    Miller, WH
    Condreay, LD
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (04) : 1005 - 1013
  • [8] INTERFERON INHIBITS HEPATITIS-B VIRUS-REPLICATION IN A STABLE EXPRESSION SYSTEM OF TRANSFECTED VIRAL-DNA
    HAYASHI, Y
    KOIKE, K
    [J]. JOURNAL OF VIROLOGY, 1989, 63 (07) : 2936 - 2940
  • [9] HISHIDA I, 1988, CHEM PHARM BULL, V36, P1819
  • [10] Global control of hepatitis B virus infection
    Kao, JH
    Chen, DS
    [J]. LANCET INFECTIOUS DISEASES, 2002, 2 (07) : 395 - 403