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Comparable Neutralization of the SARS-CoV-2 Omicron BA.1 and BA.2 Variants
Jingyou Yu; Ai-ris Collier; Marjorie Rowe; Fatima Mardas; John Ventura; Huahua Wan; Jessica Miller; Olivia Powers; Benjamin Chung; Mazuba Siamatu; Nicole Hachmann; Nehalee Surve; Felix Nampanya; Abishek Chandrashekar; Dan H. Barouch.
Afiliación
  • Jingyou Yu; Beth Israel Deaconess Medical Center
  • Ai-ris Collier; Beth Israel Deaconess Medical Center
  • Marjorie Rowe; Beth Israel Deaconess Medical Center
  • Fatima Mardas; Beth Israel Deaconess Medical Center
  • John Ventura; Beth Israel Deaconess Medical Center
  • Huahua Wan; Beth Israel Deaconess Medical Center
  • Jessica Miller; Beth Israel Deaconess Medical Center
  • Olivia Powers; Beth Israel Deaconess Medical Center
  • Benjamin Chung; Beth Israel Deaconess Medical Center
  • Mazuba Siamatu; Beth Israel Deaconess Medical Center
  • Nicole Hachmann; Beth Israel Deaconess Medical Center
  • Nehalee Surve; Beth Israel Deaconess Medical Center
  • Felix Nampanya; Beth Israel Deaconess Medical Center
  • Abishek Chandrashekar; Beth Israel Deaconess Medical Center
  • Dan H. Barouch; Beth Israel Deaconess Medical Center
Preprint en Inglés | medRxiv | ID: ppmedrxiv-22270533
ABSTRACT
The SARS-CoV-2 Omicron variant (B.1.1.529) has three major lineages BA.1, BA.2, and BA.31. BA.1 rapidly became dominant and has demonstrated substantial escape from neutralizing antibodies (NAbs) induced by vaccination2-4. BA.2 has recently increased in frequency in multiple regions of the world, suggesting that BA.2 has a selective advantage over BA.1. BA.1 and BA.2 share multiple common mutations, but both also have unique mutations1 (Fig. 1A). The ability of BA.2 to evade NAbs induced by vaccination or infection has not yet been reported. We evaluated WA1/2020, Omicron BA.1, and BA.2 NAbs in 24 individuals who were vaccinated and boosted with the mRNA BNT162b2 vaccine5 and in 8 individuals who were infected with SARS-CoV-2 (Table S1). O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=61 SRC="FIGDIR/small/22270533v1_fig1.gif" ALT="Figure 1"> O_LINKSMALLFIG WIDTH=200 HEIGHT=79 SRC="FIGDIR/small/22270533v1_fig1a.gif" ALT="Figure 1"> View larger version (26K) org.highwire.dtl.DTLVardef@1b39fc8org.highwire.dtl.DTLVardef@1bf16ceorg.highwire.dtl.DTLVardef@7248ecorg.highwire.dtl.DTLVardef@111a215_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure 1.C_FLOATNO Neutralizing antibody responses to Omicron BA.1 and BA.2. A. Cartoon showing BA.1 and BA.2 mutations in the SARS-CoV-2 Spike. NTD, N-terminal domain; RBD, receptor binding domain; RBM, receptor binding motif; SD1, subdomain 1; SD2, subdomain 2; FP, fusion peptide; HR1, heptad repeat 1; HR2, heptad repeat 2. B. Neutralizing antibody (NAb) titers by a luciferase-based pseudovirus neutralization assay in individuals two weeks following initial BNT162b2 vaccination (Prime), prior to boost (Pre-Boost), and two weeks following the third boost with BNT162b2 (Boost). C. NAb titers in 8 individuals following infection with SARS-CoV-2 Omicron BA.1, of whom 7 were vaccinated. The individual with negative NAb titers was unvaccinated and was sampled 4 days following diagnosis and hospitalization with severe COVID-19 pneumonia. Responses were measured against the SARS-CoV-2 WA1/2020, Omicron BA.1, and BA.2 variants. Medians (red bars) are depicted and shown numerically with fold differences. C_FIG O_TBL View this table org.highwire.dtl.DTLVardef@a84ecborg.highwire.dtl.DTLVardef@1cd2d42org.highwire.dtl.DTLVardef@1567410org.highwire.dtl.DTLVardef@ddcf54org.highwire.dtl.DTLVardef@56b617_HPS_FORMAT_FIGEXP M_TBL O_FLOATNOTable S1.C_FLOATNO O_TABLECAPTIONStudy population. C_TABLECAPTION C_TBL
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Texto completo: Disponible Colección: Preprints Base de datos: medRxiv Tipo de estudio: Experimental_studies Idioma: Inglés Año: 2022 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: medRxiv Tipo de estudio: Experimental_studies Idioma: Inglés Año: 2022 Tipo del documento: Preprint
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