Publication | Open Access
Serological Analysis Reveals an Imbalanced IgG Subclass Composition Associated with COVID-19 Disease Severity
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Citations
26
References
2020
Year
Unknown Venue
Covid-19 Disease SeverityDisease SusceptibilityViral DiagnosticsDisease SeverityPathogenesisImmunologyHumoral ResponseCovid-19 PandemicHumoral ImmunityRespiratory Distress SyndromeCovid-19 EpidemiologySerological Analysis RevealsPublic HealthMedicineImmune-related Gene PolymorphismViral ImmunityEpidemiologyCovid-19
Summary COVID-19 is associated with a wide spectrum of disease severity, ranging from asymptomatic to acute respiratory distress syndrome (ARDS). Paradoxically, a direct relationship has been suggested between COVID-19 disease severity, and the levels of circulating SARS-CoV-2-specific antibodies, including virus neutralizing titers. Through a serological analysis of serum samples from 536 convalescent healthcare workers, we found that SARS-CoV-2-specific and virus-neutralizing antibody levels were indeed elevated in individuals that experienced severe disease. The severity-associated increase in SARS-CoV-2-specific antibody was dominated by IgG, with an IgG subclass ratio skewed towards elevated receptor binding domain (RBD)- and S1-specific IgG3. However, RBD- and S1-specific IgG1, rather than IgG3 were best correlated with virus-neutralizing titers. We propose that Spike-specific IgG3 subclass utilization contributes to COVID-19 disease severity through potent Fc-mediated effector functions . These results have significant implications for SARS-CoV-2 vaccine design, and convalescent plasma therapy.
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