4.8 Article

SARS-CoV-2 Beta variant infection elicits potent lineage-specific and cross-reactive antibodies

期刊

SCIENCE
卷 375, 期 6582, 页码 782-+

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.abm5835

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资金

  1. Bill and Melinda Gates Foundation [INV-004923]
  2. Bavarian State Ministry of Science and the Arts
  3. Ludwig-Maximilians-Universitat Munich
  4. German Ministry for Education and Research [01KI20271, 01GM1908D]
  5. Helmholtz Association [ExNet0009-Phase2-3, HIL-A03]
  6. German Research Foundation (DFG) [FOR3004 SYNABS, PR1274/3-1, PR1274/5-1]
  7. Austrian Science Fund [FWF J4157-B30]
  8. European Union [GA101003589]
  9. German Ministry of Research [01KI2021]
  10. NaFoUniMedCovid19-COVIM [FKZ: 01KX2021]
  11. US Department of Energy (DOE) Office of Science User Facility [DE-AC02-05CH11231]
  12. DOE, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  13. DOE Office of Biological and Environmental Research
  14. National Institutes of Health, National Institute of General Medical Sciences [P41GM103393]

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The Beta variant of concern (VOC) of SARS-CoV-2 shows resistance to neutralization by antibodies from COVID-19 patients and vaccinated individuals. Researchers have identified specific antibodies in serum from Beta-infected patients that are able to cross-react with the wild type virus. This finding provides insights into the antibody response to antigenic drift and has implications for the development of future vaccines and therapeutics.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Beta variant of concern (VOC) resists neutralization by major classes of antibodies from COVID-19 patients and vaccinated individuals. In this study, serum of Beta-infected patients revealed reduced cross-neutralization of wild-type virus. From these patients, we isolated Beta-specific and cross-reactive receptor-binding domain (RBD) antibodies. The Beta-specificity results from recruitment of VOC-specific clonotypes and accommodation of mutations present in Beta and Omicron into a major antibody class that is normally sensitive to these mutations. The Beta-elicited cross-reactive antibodies share genetic and structural features with wild type-elicited antibodies, including a public VH1-58 clonotype that targets the RBD ridge. These findings advance our understanding of the antibody response to SARS-CoV-2 shaped by antigenic drift, with implications for design of next-generation vaccines and therapeutics.

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