학술논문

Mapping Neutralizing and Immunodominant Sites on the SARS-CoV-2 Spike Receptor-Binding Domain by Structure-Guided High-Resolution Serology
Document Type
article
Source
Cell. 183(4)
Subject
Medical Microbiology
Biomedical and Clinical Sciences
Immunology
Clinical Research
Lung
Pneumonia & Influenza
Biodefense
Immunization
Prevention
Infectious Diseases
Pneumonia
Vaccine Related
Emerging Infectious Diseases
Infection
Good Health and Well Being
Angiotensin-Converting Enzyme 2
Antibodies
Monoclonal
Antibodies
Neutralizing
Antibodies
Viral
Antigen-Antibody Reactions
Betacoronavirus
Binding Sites
COVID-19
Coronavirus Infections
Epitope Mapping
Epitopes
Humans
Immunoglobulin A
Immunoglobulin G
Immunoglobulin M
Kinetics
Molecular Dynamics Simulation
Pandemics
Peptidyl-Dipeptidase A
Pneumonia
Viral
Protein Binding
Protein Domains
Protein Structure
Quaternary
SARS-CoV-2
Spike Glycoprotein
Coronavirus
coronaviruses
effector functions
immunity
neutralizing antibodies
Biological Sciences
Medical and Health Sciences
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Language
Abstract
Analysis of the specificity and kinetics of neutralizing antibodies (nAbs) elicited by SARS-CoV-2 infection is crucial for understanding immune protection and identifying targets for vaccine design. In a cohort of 647 SARS-CoV-2-infected subjects, we found that both the magnitude of Ab responses to SARS-CoV-2 spike (S) and nucleoprotein and nAb titers correlate with clinical scores. The receptor-binding domain (RBD) is immunodominant and the target of 90% of the neutralizing activity present in SARS-CoV-2 immune sera. Whereas overall RBD-specific serum IgG titers waned with a half-life of 49 days, nAb titers and avidity increased over time for some individuals, consistent with affinity maturation. We structurally defined an RBD antigenic map and serologically quantified serum Abs specific for distinct RBD epitopes leading to the identification of two major receptor-binding motif antigenic sites. Our results explain the immunodominance of the receptor-binding motif and will guide the design of COVID-19 vaccines and therapeutics.