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Magnitude and breadth of neutralizing antibody responses elicited by SARS-CoV-2 infection or vaccination
Benjamin L. Sievers; Saborni Chakraborty; Yong Xue; Terri Gelbart; Joseph C. Gonzalez; Arianna G. Cassidy; Yarden Golan; Mary Prahl; Stephanie L. Gaw; Prabhu S Arunachalam; Catherine A Blish; Scott D. Boyd; Mark M Davis; Prasanna Jagannathan; Kari C. Nadeau; Bali Pulendran; Upinder Singh; Richard H. Scheuermann; Matthew H. Frieman; Sanjay Vashee; Taia T. Wang; Gene S Tan.
Afiliação
  • Benjamin L. Sievers; J. Craig Venter Institute
  • Saborni Chakraborty; Stanford University
  • Yong Xue; J. Craig Venter Institute
  • Terri Gelbart; J. Craig Venter Institute
  • Joseph C. Gonzalez; Stanford University School of Medicine
  • Arianna G. Cassidy; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California San Francisco, San Francisco, CA,
  • Yarden Golan; Department of Bioengineering and Therapeutic Sciences, and Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA
  • Mary Prahl; Division of Pediatric Infectious Diseases, Department of Pediatrics, University of California, San Francisco, CA, USA.
  • Stephanie L. Gaw; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California San Francisco, San Francisco, CA,
  • Prabhu S Arunachalam; Stanford University
  • Catherine A Blish; Stanford University
  • Scott D. Boyd; Stanford University
  • Mark M Davis; Stanford University
  • Prasanna Jagannathan; Stanford University
  • Kari C. Nadeau; Stanford University
  • Bali Pulendran; Stanford University
  • Upinder Singh; Stanford University
  • Richard H. Scheuermann; J. Craig Venter Institute
  • Matthew H. Frieman; University of Maryland School of Medicine
  • Sanjay Vashee; J. Craig Venter Institute
  • Taia T. Wang; Stanford University School of Medicine
  • Gene S Tan; J. Craig Venter Institute
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21268540
ABSTRACT
Multiple SARS-CoV-2 variants that possess mutations associated with increased transmission and antibody escape have arisen over the course of the current pandemic. While the current vaccines have largely been effective against past variants, the number of mutations found on the Omicron (B.1.529) spike appear to diminish the efficacy of pre-existing immunity. Using pseudoparticles expressing the spike of several SARS-CoV-2 variants, we evaluated the magnitude and breadth of the neutralizing antibody response over time in naturally infected and in mRNA-vaccinated individuals. We observed that while boosting increases the magnitude of the antibody response to wildtype (D614), Beta, Delta and Omicron variants, the Omicron variant was the most resistant to neutralization. We further observed that vaccinated healthy adults had robust and broad antibody responses while responses were relatively reduced in vaccinated pregnant women, underscoring the importance of learning how to maximize mRNA vaccine responses in pregnant populations. Findings from this study show substantial heterogeneity in the magnitude and breadth of responses after infection and mRNA vaccination and may support the addition of more conserved viral antigens to existing SARS-CoV-2 vaccines. One Sentence SummaryDiminished efficacy of pre-existing immunity to highly mutated SARS-CoV-2 variants.
Licença
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Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint