Fc-mediated functions of nirsevimab complement direct respiratory syncytial virus neutralization but are not required for optimal prophylactic protection
Authors:
Brady, Tyler et al. Frontiers in Immunology, Volume 14, 1283120.
Journal:
Frontiers in Immunology
Journal Abstract:
Nirsevimab is an extended half-life (M252Y/S254T/T256E [YTE]- modified) monoclonal antibody to the pre-fusion conformation of the respiratory syncytial virus (RSV) Fusion protein, with established efficacy in preventing RSV-associated lower respiratory tract infection in infants for the duration of a typical RSV season. Previous studies suggest that nirsevimab confers protection via direct virus neutralization. Here we use preclinical models to explore whether fragment crystallizable (Fc)-mediated effector functions contribute to nirsevimab-mediated protection.