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Abstract The rodent-borne Andes virus (ANDV) causes a severe disease in humans. We developed an ANDV mRNA vaccine based on the M segment of the viral genome, either with regular uridine (U-mRNA) or N1-methylpseudouridine (m1Ψ-mRNA). Female mice immunized by m1Ψ-mRNA developed slightly greater germinal center (GC) responses than U-mRNA-immunized mice.
Abstract The COVID-19 pandemic underscored the promise of monoclonal antibody-based prophylactic and therapeutic drugs1,2,3 and revealed how quickly viral escape can curtail effective options4,5. When the SARS-CoV-2 Omicron variant emerged in 2021, many antibody drug products lost potency, including Evusheld and its constituent, cilgavimab4,5,6.
Cell lines Expi293F cells (human, female origin) were cultured in suspension at 37 °C in 8% CO2 with shaking at 125 r.p.m. in Freestyle F17 Expression Medium (Gibco) supplemented with 10% Pluronic F-68 and 200 mM of l-glutamine. ExpiCHO cells (hamster, female origin) were cultured in suspension at 37 °C in 8% CO2 with shaking at 125 r.p.m. in ExpiCHO Expression Medium (Thermo Fisher).
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