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. 2017 Aug 15;7:8267. doi: 10.1038/s41598-017-07434-y

Figure 3.

Figure 3

HEV is more sensitive than HBV to pegIFNα treatment in human-liver chimeric mice. HEV RNA was measured by qRT-PCR in feces of human-liver chimeric mice infected with HEV gt3 or HEV gt1 before and during 4 weeks (a, n = 3), 2 weeks (b, n = 4; e, n = 3). and single (c, n = 4) pegIFNα treatment. Horizontal gray bars indicate pegIFNα treatment duration and dosage in µg/kg (a,b). Arrow indicates time point of the single 30 µg/kg pegIFNα injection (c). One day after last dosage mice were sacrificed and viral load was determined in liver and bile (d). Non-treated infected mice were added as control (d). X-axes indicates number of pegIFNα injections (d). HBV DNA was measured in serum of HBV gtA infected human-liver chimeric mice before and during pegIFNα treatment, and one day after last treatment mice were euthanized and intrahepatic HBV DNA was measured (f, n = 6). #indicates 3 µg/kg pegIFNα dosages. All mice were transplanted with the same hepatocyte donor (HD2, af). Y-axes indicate log HEV RNA IU/gram (ac,d left panel, e), log HEV RNA IU/ml (d right panel), and log HBV DNA copies/ml (f). X-axes indicate days post infection (ac,ef).