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Plasma neutralization properties of the SARS-CoV-2 Omicron variant
Fabian Schmidt; Frauke Muecksch; Yiska Weisblum; Justin Da Silva; Eva Bednarski; Alice Cho; Zijun Wang; Christian Gaebler; Marina Caskey; Michel Nussenzweig; Theodora Hatziioannou; Paul Bieniasz.
Afiliación
  • Fabian Schmidt; The Rockefeller University
  • Frauke Muecksch; The Rockefeller University
  • Yiska Weisblum; The Rockefeller University
  • Justin Da Silva; The Rockefeller University
  • Eva Bednarski; The Rockefeller University
  • Alice Cho; The Rockefeller University
  • Zijun Wang; The Rockefeller University
  • Christian Gaebler; The Rockefeller University
  • Marina Caskey; The Rockefeller University
  • Michel Nussenzweig; The Rockefeller University
  • Theodora Hatziioannou; The Rockefeller University
  • Paul Bieniasz; The Rockefeller University
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21267646
ABSTRACT
BACKGROUNDThe Omicron SARS-CoV-2 variant has spread internationally and is responsible for rapidly increasing case numbers. The emergence of divergent variants in the context of a heterogeneous and evolving neutralizing antibody response in host populations might compromise protection afforded by vaccines or prior infection. METHODSWe measured neutralizing antibody titers in 169 longitudinally collected plasma samples using pseudotypes bearing the Wuhan-hu-1 or the Omicron variant or a laboratory-designed neutralization-resistant SARS-CoV-2 spike (PMS20). Plasmas were obtained from convalescents who did or did not subsequently receive an mRNA vaccine, or naive individuals who received 3-doses of mRNA or 1-dose Ad26 vaccines. Samples were collected approximately 1, 5-6 and 12 months after initial vaccination or infection. RESULTSLike PMS20, the Omicron spike protein was substantially resistant to neutralization compared to Wuhan-hu-1. In convalescent plasma the median deficit in neutralizing activity against PMS20 or Omicron was 30- to 60-fold. Plasmas from recipients of 2 mRNA vaccine doses were 30- to 180- fold less potent against PMS20 and Omicron than Wuhan-hu-1. Notably, previously infected or two-mRNA dose vaccinated individuals who received additional mRNA vaccine dose(s) had 38 to 154-fold and 35 to 214-fold increases in neutralizing activity against Omicron and PMS20 respectively. CONCLUSIONSOmicron exhibits similar distribution of sequence changes and neutralization resistance as does a laboratory-designed neutralization-resistant spike protein, suggesting natural evolutionary pressure to evade the human antibody response. Currently available mRNA vaccine boosters, that may promote antibody affinity maturation, significantly ameliorate SARS-CoV-2 neutralizing antibody titers.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Idioma: En Año: 2021 Tipo del documento: Preprint