Copyright
©The Author(s) 2015.
World J Hepatol. Aug 28, 2015; 7(18): 2177-2183
Published online Aug 28, 2015. doi: 10.4254/wjh.v7.i18.2177
Published online Aug 28, 2015. doi: 10.4254/wjh.v7.i18.2177
Table 1 Primers specific for the hepatitis C virus NS3/4A protease gene sequence used for polymerase chain reaction
HCV genotype 1 | Primers | Sequences 5'-3' | H77 location |
G1F1 | CTB CTS GGR CCR GCC GAT | 3372-3390 | |
G1R1 | CCA CYT GGW AKS TCT GSG G | 3998-4016 | |
MarsF3 | ACS GCR GCR TGY GGG GAC AT | 3309-3328 | |
MarsR2 | GTG CTC TTR CCG CTR CCR GT | 4035-4054 |
Table 2 Patient characteristics at initiation of triple anti-hepatitis C virus therapy (n = 41)
Age: median (IQR) | 51 (48-55) |
Male gender | 35 (85.4%) |
Genotype | |
1a | 32 (78.0%) |
1b | 9 (22.0%) |
HCV treatment-naïve | 13 (31.7%) |
Prior HCV-treatment response | |
Non-responders | 14 (34.1%) |
Breakthrough | 1 (2.5%) |
Relapse | 5 (12.2%) |
Premature treatment discontinuation | 3 (4.9%) |
Missing data | 5 (14.6%) |
Log HCV-RNA | 5.8 (5.3-6.1) |
Fibrosis stage | |
F0-F1 | 12 (29.3%) |
F2 | 7 (17.0%) |
F3 | 5 (12.2%) |
F4 | 17 (41.5%) |
CD4 T-cells/mm3: median (IQR) | 540 (441-782) |
HIV-RNA < 40 copies/mL | 41 (100.0%) |
Table 3 Main adverse events in 40 patients with available follow-up
Rash | 10 (25%) |
Anemia Hb < 13 g/dL (men), < 12 g/dL (women) | 39 (98%) |
Severe anemia (< 9 g/dL or decrease > 3 g/dL) | 35 (88%) |
Ribavirin dose decreased | 23 (58%) |
EPO administration | 23 (58%) |
Blood transfusion | 2 (5%) |
Table 4 Baseline and post treatment NS3/4A-mutations among patients failing hepatitis C virus treatment
Genotype | Previouslytreated | HCV PI | Response totreatment | HIV PI | Pre-treatmentHCV VL | Baseline NS3/4A-mutations | Baselinefold-change | Post-treatmentNS3/4A-mutations | Post-treatmentfold change1 |
1a | Yes | Tela | Non-responder | Atazanavir | 5.9 | 0 | V36M, R155K | 62 | |
1a | Yes | Tela | Non-responder | 0 | 5.8 | 0 | V36M, R155K | 62 | |
1a | Yes | Tela | Breakthrough | Atazanavir | 6.0 | 0 | R155K | 7.4 | |
1a | Yes | Tela | Breakthrough | Atazanavir | 6.5 | 0 | V36M | 6.8-10.0 | |
1a | No | Tela | Breakthrough | Atazanavir | 6.0 | 0 | V36M, R155K | 62 | |
1b | Yes | Tela | Relapse | Atazanavir | 6.4 | I132V | 1.8 | I132V, V36A | 7.4-7.5 |
1a | No | Tela | Relapse | 0 | 6.3 | I132V | 1.8 | I132V, V36A | 7.4-7.5 |
1b | No | Tela | Relapse | 0 | 4.9 | I132V | 1.8 | I132V, V36A | 7.4-7.5 |
1a | NA | Boce | Relapse | Darunavir | NA | NA | NA | T54S, R155K | 8.5 |
- Citation: Naqvi A, Giordanengo V, Dunais B, de Salvador-Guillouet F, Perbost I, Durant J, Pugliese P, Joulié A, Roger PM, Rosenthal E. Virological response and resistance mutations to NS3/4A inhibitors in hepatitis C virus-human immunodeficiency virus coinfection. World J Hepatol 2015; 7(18): 2177-2183
- URL: https://www.wjgnet.com/1948-5182/full/v7/i18/2177.htm
- DOI: https://dx.doi.org/10.4254/wjh.v7.i18.2177