作者
Deidre Wilkins,Anne Greenough,Robert Jan Lebbink,Christopher Morehouse,Michael E. Abram,Bahar Ahani,Anastasia A. Aksyuk,Eugenio Baraldi,Tyler Brady,Albert T. Chen,Hsin Chi,Eun Hwa Choi,Robert Cohen,Daria Danilenko,Vancheswaran Gopalakrishnan,Anne Greenough,Terho Heikkinen,Mitsuaki Hosoya,Christian Keller,Elizabeth J. Kelly,Leyla Kragten‐Tabatabaie,Federico Martinón‐Torres,Abiel Homero Mascareñas de Los Santos,Marta C. Nunes,María Angélica Palomino,Jesse Papenburg,Jeffrey M. Pernica,Peter Richmond,Renato T. Stein,Kevin M. Tuffy,Charl Verwey,Mark T. Esser,David E. Tabor,Louis Bont,Pascale Marro Clément,Atul Gupta,Koichi Hashimoto,Kseniya Komissarova,Matt Laubscher,Magali Santos Lumertz,Elena Priante,Irene Rivero‐Calle,Ushma Wadia,Ki Wook Yun
摘要
Nirsevimab is an extended half-life monoclonal antibody to the respiratory syncytial virus (RSV) fusion protein that has been developed to protect infants for an entire RSV season. Previous studies have shown that the nirsevimab binding site is highly conserved. However, investigations of the geotemporal evolution of potential escape variants in recent (ie, 2015-2021) RSV seasons have been minimal. Here, we examine prospective RSV surveillance data to assess the geotemporal prevalence of RSV A and B, and functionally characterise the effect of the nirsevimab binding-site substitutions identified between 2015 and 2021.