Hepatitis C Virus Variants with Decreased Sensitivity to Direct-Acting Antivirals (DAAs) Were Rarely Observed in DAA-Naive Patients prior to Treatment

被引:126
作者
Bartels, Doug J. [1 ]
Sullivan, James C. [1 ]
Zhang, Eileen Z. [1 ]
Tigges, Ann M. [1 ]
Dorrian, Jennifer L. [1 ]
De Meyer, Sandra [2 ]
Takemoto, Darin [1 ]
Dondero, Elizabeth [1 ]
Kwong, Ann D. [1 ]
Picchio, Gaston [3 ]
Kieffer, Tara L. [1 ]
机构
[1] Vertex Pharmaceut Inc, Dept Infect Dis, Cambridge, MA USA
[2] Janssen Infect Dis, Beerse, Belgium
[3] Janssen Res & Dev, Titusville, NJ USA
关键词
IN-VITRO RESISTANCE; PROTEASE INHIBITOR; POLYMERASE INHIBITOR; COMBINATION THERAPY; INFECTED PATIENTS; CROSS-RESISTANCE; TELAPREVIR; MUTATIONS; IDENTIFICATION; RETREATMENT;
D O I
10.1128/JVI.02294-12
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
The prevalence of naturally occurring hepatitis C virus (HCV) variants that are less sensitive to direct-acting antiviral (DAA) inhibitors has not been fully characterized. We used population sequence analysis to assess the frequency of such variants in plasma samples from 3,447 DAA-naive patients with genotype 1 HCV. In general, HCV variants with lower-level resistance (3- to 25-fold increased 50% inhibitor concentration [IC50]) to telaprevir were observed as the dominant species in 0 to 3% of patients, depending on the specific variant, whereas higher-level resistant variants (>25-fold-increased IC50) were not observed. Specific variants resistant to NS5A inhibitors were predominant in up to 6% of patients. Most variants resistant to nucleo(s/t)ide active-site NS5B polymerase inhibitors were not observed, whereas variants resistant to non-nucleoside allosteric inhibitors were observed in up to 18% of patients. The presence of DAA-resistant variants in NS5A, NS5B, or NS3 (including telaprevir-resistant variants), in baseline samples of treatment-naive patients receiving a telaprevir-based regimen in phase 3 studies did not affect the sustained viral response (SVR). Treatment-naive patients with viral populations containing the telaprevir-resistant variants NS3 V36M, T54S, or R155K at baseline achieved a 74% SVR rate, whereas patients with no resistant variants detected prior to treatment achieved a 76% SVR rate. The effect of specific resistant variant frequency on response to various DAA treatments in different patient populations, including interferon nonresponders, should be further studied.
引用
收藏
页码:1544 / 1553
页数:10
相关论文
共 66 条
[1]
A Multi-Variant, Viral Dynamic Model of Genotype 1 HCV to Assess the in vivo Evolution of Protease-Inhibitor Resistant Variants [J].
Adiwijaya, Bambang S. ;
Herrmann, Eva ;
Hare, Brian ;
Kieffer, Tara ;
Lin, Chao ;
Kwong, Ann D. ;
Garg, Varun ;
Randle, John C. R. ;
Sarrazin, Christoph ;
Zeuzem, Stefan ;
Caron, Paul R. .
PLOS COMPUTATIONAL BIOLOGY, 2010, 6 (04)
[2]
Selected Replicon Variants with Low-Level In Vitro Resistance to the Hepatitis C Virus NS5B Polymerase Inhibitor PSI-6130 Lack Cross-Resistance with R1479 [J].
Ali, Samir ;
Leveque, Vincent ;
Le Pogam, Sophie ;
Ma, Han ;
Philipp, Friederike ;
Inocencio, Nicole ;
Smith, Mark ;
Alker, Andre ;
Kang, Hyunsoon ;
Najera, Isabel ;
Klumpp, Klaus ;
Symons, Julian ;
Cammack, Nick ;
Jiang, Wen-Rong .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (12) :4356-4369
[3]
[Anonymous], 2011, VICTR US PRESCR INF
[4]
Susceptibility of Treatment-Naive Hepatitis C Virus (HCV) Clinical Isolates to HCV Protease Inhibitors [J].
Bae, Andrew ;
Sun, Siu-Chi ;
Qi, Xiaoping ;
Chen, Xiaowu ;
Ku, Karin ;
Worth, Angela ;
Wong, Kelly A. ;
Harris, Jeanette ;
Miller, Michael D. ;
Mo, Hongmei .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (12) :5288-5297
[5]
Bartels D, 2010, 5 INT WORKSH HEP C R
[6]
Natural prevalence of hepatitis C virus variants with decreased sensitivity to NS3•4A protease inhibitors in treatment-naive subjects [J].
Bartels, Doug J. ;
Zhou, Yi ;
Zhang, Eileen Z. ;
Marcial, Michelle ;
Byrn, Randal A. ;
Pfeiffer, Thomas ;
Tigges, Ann M. ;
Adiwijaya, Bambang S. ;
Lin, Chao ;
Kwong, Ann D. ;
Kieffer, Tara L. .
JOURNAL OF INFECTIOUS DISEASES, 2008, 198 (06) :800-807
[7]
Recent advances in the development of NS5B polymerase inhibitors for the treatment of hepatitis C virus infection [J].
Beaulieu, Pierre L. .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2009, 19 (02) :145-164
[8]
Inhibition of hepatitis C virus RNA replication by 2′-modified nucleoside analogs [J].
Carroll, SS ;
Tomassini, JE ;
Bosserman, M ;
Getty, K ;
Stahlhut, MW ;
Eldrup, AB ;
Bhat, B ;
Hall, D ;
Simcoe, AL ;
LaFemina, R ;
Rutkowski, CA ;
Wolanski, B ;
Yang, ZC ;
Migliaccio, G ;
De Francesco, R ;
Kuo, LC ;
MacCoss, M ;
Olsen, DB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (14) :11979-11984
[9]
Identification of the minimal conserved structure of HIV-1 protease in the presence and absence of drug pressure [J].
Ceccherini-Silberstein, F ;
Erba, F ;
Gago, F ;
Bertoli, A ;
Forbici, F ;
Bellocchi, MC ;
Gori, C ;
d'Arrigo, R ;
Marcon, L ;
Balotta, C ;
Antinori, A ;
Monforte, AD ;
Perno, CF .
AIDS, 2004, 18 (12) :F11-F19
[10]
Resistance Analysis of the Hepatitis C Virus NS5A Inhibitor BMS-790052 in an In Vitro Replicon System [J].
Fridell, Robert A. ;
Qiu, Dike ;
Wang, Chunfu ;
Valera, Lourdes ;
Gao, Min .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (09) :3641-3650