Table 2.
Patient | ρT (day-1) | δ (day-1) | μ (10-6) | εs | εr | β (10-8 mL day-1 virion-1) | ps (virions cell-1 day-1) | r | Infected cells at baseline* (%) | Increase in total hepatocytes (%) |
---|---|---|---|---|---|---|---|---|---|---|
1002 | 1.91 | 0.52 | 2.68 | 0.99943 | 0.001 | 4.30 | 44.36 | 0.80 | 16 | 32 |
1018 | 2.38 | 0.41 | 13.91 | 0.99982 | 0.036 | 0.58 | 131.08 | 0.70 | 16 | 11 |
3006 | 2.50 | 0.50 | 5.98 | 0.99548 | 0.003 | 11.21 | 6.60 | 0.97 | 11 | 7 |
3017 | 1.21 | 0.32 | 1.99 | 0.99965 | 0.002 | 19.41 | 6.17 | 0.84 | 16 | 32 |
Average±SD | 2.00±0.59 | 0.44±0.09 | 6.14±5.46 | 0.99860±0.00210 | 0.011±0.017 | 8.88±8.29 | 47.05±58.81 | 0.83±0.11 | 15±2.5 | 21±13 |
During data fitting, we assumed that half the maximum number of hepatocytes are not targets of HCV infection (N=Tmax/2). With this assumption, about 15% of hepatocytes were infected before treatment, consistent with the experimental results in (25, 26). Using a smaller N, e.g., N=Tmax/4, we will have a higher percentage of infected cells at baseline and an unrealistic increase in the total number of hepatocytes after 14-day treatment. Using a larger N, e.g., N=3Tmax/4, we could not obtain good fits because of limited replication space for drug-resistant virus.