Resistance mechanisms in HCV: from evolution to intervention

被引:14
作者
Kim, Arthur Y. [2 ]
Timm, Joerg [1 ]
机构
[1] Univ Duisburg Essen, Dept Virol, D-45147 Essen, Germany
[2] Harvard Univ, Partners AIDS Res Ctr, Massachusetts Gen Hosp, Sch Med, Charlestown, MA 02129 USA
关键词
hepatitis C virus; polymerase inhibitor; protease inhibitor; quasispecies; resistance mutation; selection pressure; viral fitness;
D O I
10.1586/14787210.6.4.463
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Recent advances in our understanding of the HCV life cycle and the functions of virally encoded proteins enabled the development of specifically targeted antiviral therapies for HCV, which directly inhibit HCV replication. Early clinical trials show great efficacy; however, from the first trials it became evident that, similar to HIV and HBV, selection of resistant variants will be problematic. Error-prone replication of HCV, resulting in a complex quasispecies population within each infected individual, enables rapid adaptation to changing environments. In this review, the evolutionary mechanisms involved in the selection process resulting in drug resistance are discussed. We give an overview of the resistance profiles to recently developed HCV protease and polymerase inhibitors and discuss potential implications for future treatment developments.
引用
收藏
页码:463 / 478
页数:16
相关论文
共 94 条
[1]  
Afdhal N, 2004, HEPATOLOGY, V40, p726A
[2]   Evolution of hepatitis C virus quasispecies during ribavirin and interferon-alpha-2b combination therapy and interferon-alpha-2b monotherapy [J].
Arataki, Keiko ;
Kumada, Hiromitsu ;
Toyota, Kiyomi ;
Ohishi, Waka ;
Takahashi, Shoichi ;
Tazuma, Susumu ;
Chayama, Kazuaki .
INTERVIROLOGY, 2006, 49 (06) :352-361
[3]   Efficient initiation of HCV RNA replication in cell culture [J].
Blight, KJ ;
Kolykhalov, AA ;
Rice, CM .
SCIENCE, 2000, 290 (5498) :1972-1974
[4]   Hepatitis C Virus Diversity and Evolution in the Full Open-Reading Frame during Antiviral Therapy [J].
Cannon, Nathan A. ;
Donlin, Maureen J. ;
Fan, Xiaofeng ;
Aurora, Rajeev ;
Tavis, John E. .
PLOS ONE, 2008, 3 (05) :1-12
[5]   Quasispecies heterogeneity within the E1/E2 region as a pretreatment variable during pegylated interferon therapy of chronic hepatitis C virus infection [J].
Chambers, TJ ;
Fan, XF ;
Droll, DA ;
Hembrador, E ;
Slater, T ;
Nickells, MW ;
Dustin, LB ;
DiBisceglie, AM .
JOURNAL OF VIROLOGY, 2005, 79 (05) :3071-3083
[6]  
Chandra P, 2006, GASTROENTEROLOGY, V130, pA748
[7]   Pretreatment virus load and multiple amino acid substitutions in the interferon sensitivity-determining region predict the outcome of interferon treatment in patients with chronic genotype 1b hepatitis C virus infection [J].
Chayama, K ;
Tsubota, A ;
Kobayashi, M ;
Okamoto, K ;
Hashimoto, M ;
Miyano, Y ;
Koike, H ;
Kobayashi, M ;
Koida, I ;
Arase, Y ;
Saitoh, S ;
Suzuki, Y ;
Murashima, N ;
Ikeda, K ;
Kumada, H .
HEPATOLOGY, 1997, 25 (03) :745-749
[8]   Activity of a potent hepatitis C virus polymerase inhibitor in the chimpanzee model [J].
Chen, Chih-Ming ;
He, Yupeng ;
Lu, Liangjun ;
Ben Lim, Hock ;
Tripathi, Rakesh L. ;
Middleton, Tim ;
Hernandez, Lisa E. ;
Beno, David W. A. ;
Long, Michelle A. ;
Kati, Warren M. ;
Bosse, Todd D. ;
Larson, Daniel P. ;
Wagner, Rolf ;
Lanford, Robert E. ;
Kohlbrenner, William E. ;
Kempf, Dale J. ;
Pilot-Matias, Tami J. ;
Molla, Akhteruzzaman .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (12) :4290-4296
[9]   Construction of hepatitis C-SIN virus recombinants with replicative dependency on hepatitis C virus serine protease activity [J].
Cho, YG ;
Moon, HS ;
Sung, YC .
JOURNAL OF VIROLOGICAL METHODS, 1997, 65 (02) :201-207
[10]   Natural presence of substitution R155K within hepatitis C virus NS3 protease from a treatment-naive chronically infected patient [J].
Colson, Philippe ;
Brouk, Nabil ;
Lembo, Frederique ;
Castellani, Paul ;
Tamalet, Catherine ;
Gerolami, Rene .
HEPATOLOGY, 2008, 47 (02) :766-767