Fig. 4: Virus titration and quantitation in the lower respiratory tract of animal models.
From: A therapeutic neutralizing antibody targeting receptor binding domain of SARS-CoV-2 spike protein

Three ferrets per group were euthanized at 3 and 7 dpi, and lungs were collected to measure viral titers (a) and the number of viral RNA copies (d). Golden Syrian hamsters (n = 12/group) were challenged intranasally with 6.4 × 104 PFU/80 μL of SARS-CoV-2. Vehicle and 15, 30, 60, and 90 mg/kg of CT-P59 were intraperitoneally administered 24 h after virus inoculation. Four animals were euthanized for virus titration (b) and quantitation of viral RNA copies (e) from each group at 3 and 5 dpi. Rhesus monkeys (control n = 3, 45 mg/kg n = 2, 90 mg/kg n = 3) were infected with 106.4 TCID50/ml of SARS-CoV-2 via in a combination of intranasal (0.5 ml), intratracheal (4 ml), ocular (0.25 ml/eye), and oral (1 ml) routes. Vehicle, 45 mg/kg and 90 mg/kg of CT-P59 were administered intravenously after 24 h of virus infection. All rhesus monkeys were euthanized at 6 dpi, and lungs were collected to measure viral titers (c) and the number of viral RNA copies (f). Viral titers in the lung were determined by TCID50 assessment in Vero cells and viral RNA copy number measurement using qRT-PCR. Viral titers and RNA copy numbers are shown as mean value + /− SEM and titers below the limit of detection are shown as 0.8 log10TCID50/ml or 0.3 log10 viral RNA copies/ml (dashed lines). Asterisks indicate statistical significance between the control and each group as determined by two-way ANOVA and subsequent Dunnett’s test. *P = 0.0309, **P = 0.0131, and ***P < 0.0001 (a); *P = 0.0002 and **P < 0.0001 (b); *P = 0.0329 (d); and *P = 0.0123, **P = 0.0025, ***P = 0.0003, and ****P = 0.0002 (e).