Perspectives for the treatment of infections with Flaviviridae

被引:135
作者
Leyssen, P [1 ]
De Clercq, E [1 ]
Neyts, J [1 ]
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, Dept Chemotherapy, B-3000 Louvain, Belgium
关键词
D O I
10.1128/CMR.13.1.67-82.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The family Flaviviridae contains three genera: Hepacivirus, Flavivirus, and Pestivirus. Worldwide more than 170 million people are chronically infected with Hepatitis C virus and am at risk of developing cirrhosis and/or liver cancer. In addition, infections with arthropod-borne flaviviruses (such as dengue fever, Japanese encephalitis, tick-borne encephalitis, St. Louis encephalitis, Murray Valley encephalitis, West Nile, and yellow fever viruses) are emerging throughout the world. The pestiviruses have a serious impact an livestock Unfortunately, no specific antiviral therapy is available far the treatment or the prevention of infections with members of the Flaviviridae. Ongoing research has identified possible targets for inhibition, including binding of the virus to the cell, uptake of the virus into the cell the internal ribosome entry site of hepaciviruses and pestiviruses, the capping mechanism of flaviviruses, the viral proteases, the viral RNA-dependent RNA polymerase, and the viral helicase lit light of recent developments, the prevalence of infections caused by these viruses, the disease spectrum, and the impact of infections different strategies that could be pursued to specifically inhibit viral targets and animal models that are available to study the pathogenesis and antiviral strategies are reviewed.
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页码:67 / +
页数:17
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共 260 条
[1]   Expression of recombinant hepatitis C virus non-structural protein 5B in Escherichia coli [J].
Al, RH ;
Xie, YP ;
Wang, YH ;
Hagedorn, CH .
VIRUS RESEARCH, 1998, 53 (02) :141-149
[2]   Core specific antisense phosphorothioate oligodeoxynucleotides as potent and specific inhibitors of hepatitis C viral translation [J].
Alt, M ;
Renz, R ;
Hofschneider, PH ;
Caselmann, WH .
ARCHIVES OF VIROLOGY, 1997, 142 (03) :589-599
[3]   Hepatitis C [J].
Alter, MJ ;
Mast, EE ;
Moyer, LA ;
Margolis, HS .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 1998, 12 (01) :13-+
[4]   INVITRO ACTIVITY OF PIRODAVIR (R-77975), A SUBSTITUTED PHENOXY-PYRIDAZINAMINE WITH BROAD-SPECTRUM ANTIPICORNAVIRAL ACTIVITY [J].
ANDRIES, K ;
DEWINDT, B ;
SNOEKS, J ;
WILLEBRORDS, R ;
VANEEMEREN, K ;
STOKBROEKX, R ;
JANSSEN, PAJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (01) :100-107
[5]  
ANGUSBHAKORN S, 1987, J VIROL METHODS, V18, P13
[6]  
ARROYO JI, 1988, AM J TROP MED HYG, V38, P647
[7]   Molecular medicine - Antisense oligonucleotide therapy [J].
Askari, FK ;
McDonnell, WM .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (05) :316-318
[8]  
BAKER JC, 1987, J AM VET MED ASSOC, V190, P1449
[9]   ALPHA-(1-3)-D-MANNOSE-SPECIFIC AND ALPHA-(1-6)-D-MANNOSE-SPECIFIC PLANT-LECTINS ARE MARKEDLY INHIBITORY TO HUMAN-IMMUNODEFICIENCY-VIRUS AND CYTOMEGALOVIRUS INFECTIONS INVITRO [J].
BALZARINI, J ;
SCHOLS, D ;
NEYTS, J ;
VANDAMME, E ;
PEUMANS, W ;
DECLERCQ, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (03) :410-416
[10]   THE MANNOSE-SPECIFIC PLANT-LECTINS FROM CYMBIDIUM HYBRID AND EPIPACTIS-HELLEBORINE AND THE (N-ACETYLGLUCOSAMINE)N-SPECIFIC PLANT LECTIN FROM URTICA-DIOICA ARE POTENT AND SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS AND CYTOMEGALOVIRUS REPLICATION INVITRO [J].
BALZARINI, J ;
NEYTS, J ;
SCHOLS, D ;
HOSOYA, M ;
VANDAMME, E ;
PEUMANS, W ;
DECLERCQ, E .
ANTIVIRAL RESEARCH, 1992, 18 (02) :191-207