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Mapping SARS-CoV-2 antigenic relationships and serological responses
Samuel H Wilks; Barbara Muhlemann; Xiaoying Shen; Sina Tureli; Eric B LeGresley; Antonia Netzl; Jesus N Chacaltana-Huarcaya; Victor M Corman; Xiaoju Daniell; Michael B Datto; Fatimah S Dawood; Thomas N Denny; Christian Drosten; Ron A M Fouchier; Patricia J Garcia; Peter J Halfmann; Agatha Jassem; Lara M Jeworowski; Terry C Jones; Yoshihiro Kawaoka; Florian Krammer; Charlene McDanal; Rolando Pajon; Viviana Simon; Melissa Stockwell; Haili Tang; Harm van Bakel; Vic Veguilla; David C Montefiori; Derek J Smith.
Affiliation
  • Samuel H Wilks; Center for Pathogen Evolution, Department of Zoology, University of Cambridge
  • Barbara Muhlemann; Institute of Virology, Charite - Universitatsmedizin Berlin; German Centre for Infection Research (DZIF), partner site Charite
  • Xiaoying Shen; Department of Surgery, Duke University School of Medicine; Duke Human Vaccine Institute, Duke University School of Medicine
  • Sina Tureli; Center for Pathogen Evolution, Department of Zoology, University of Cambridge
  • Eric B LeGresley; Center for Pathogen Evolution, Department of Zoology, University of Cambridge
  • Antonia Netzl; Center for Pathogen Evolution, Department of Zoology, University of Cambridge
  • Jesus N Chacaltana-Huarcaya; Hospital Nacional Daniel A Carrion
  • Victor M Corman; Institute of Virology, Charite - Universitatsmedizin Berlin; German Centre for Infection Research (DZIF), partner site Charite
  • Xiaoju Daniell; Department of Surgery, Duke University School of Medicine
  • Michael B Datto; Department of Pathology, Duke University School of Medicine
  • Fatimah S Dawood; Centers for Disease Control and Prevention, Atlanta, GA, USA
  • Thomas N Denny; Department of Surgery, Duke University School of Medicine
  • Christian Drosten; Institute of Virology, Charite - Universitatsmedizin Berlin; German Centre for Infection Research (DZIF), partner site Charite
  • Ron A M Fouchier; Erasmus Medical Center
  • Patricia J Garcia; School of Public Health, Universidad Peruana Cayetano Heredia
  • Peter J Halfmann; Department of Pathobiological Science, School of Veterinary Medicine University of Wisconsin-Madison
  • Agatha Jassem; BC Centre for Disease Control
  • Lara M Jeworowski; Institute of Virology, Charite - Universitatsmedizin Berlin; German Centre for Infection Research (DZIF), partner site Charite
  • Terry C Jones; Center for Pathogen Evolution, Department of Zoology, University of Cambridge; Institute of Virology, Charite - Universitatsmedizin Berlin; German Centre for In
  • Yoshihiro Kawaoka; Department of Pathobiological Science, School of Veterinary Medicine University of Wisconsin-Madison; Division of Virology, Institute of Medical Science, Univer
  • Florian Krammer; Department of Microbiology, Icahn School of Medicine at Mount Sinai; Department of Pathology, Cellular and Molecular Medicine, Icahn School of Medicine at Mount
  • Charlene McDanal; Department of Surgery, Duke University School of Medicine
  • Rolando Pajon; Moderna, Inc.
  • Viviana Simon; Department of Microbiology, Icahn School of Medicine at Mount Sinai; Department of Pathology, Cellular and Molecular Medicine, Icahn School of Medicine at Mount
  • Melissa Stockwell; Division of Child and Adolescent Health, Department of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons, and Department of Population
  • Haili Tang; Department of Surgery, Duke University School of Medicine
  • Harm van Bakel; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai
  • Vic Veguilla; Centers for Disease Control and Prevention, Atlanta, GA, USA
  • David C Montefiori; Department of Surgery, Duke University School of Medicine; Duke Human Vaccine Institute, Duke University School of Medicine
  • Derek J Smith; Center for Pathogen Evolution, Department of Zoology, University of Cambridge
Preprint in English | bioRxiv | ID: ppbiorxiv-477987
ABSTRACT
During the SARS-CoV-2 pandemic, multiple variants with differing amounts of escape from pre-existing immunity have emerged, causing concerns about continued protection. Here, we use antigenic cartography to quantify and visualize the antigenic relationships among 16 SARS-CoV-2 variants titrated against serum samples taken post-vaccination and post-infection with seven different variants. We find major antigenic differences caused by substitutions at spike positions 417, 452, 484, and possibly 501. B.1.1.529 (Omicron BA.1) showed the highest escape from all sera tested. Visualization of serological responses as antibody landscapes shows how reactivity clusters in different regions of antigenic space. We find changes in immunodominance of different spike regions depending on the variant an individual was exposed to, with implications for variant risk assessment and vaccine strain selection. One sentence summaryAntigenic Cartography of SARS-CoV-2 variants reveals amino acid substitutions governing immune escape and immunodominance patterns.
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Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Prognostic study Language: English Year: 2022 Document type: Preprint
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