medRxiv · 2020 · 77 citations · 23 references
Life SciencesImmunologyInfectious DiseasesAdaptive ImmunityClinical ImmunologyImmunology Of Infectious DiseasesAntiviral ImmunityHumoral ImmunityImmune Responses To InfectionImmune-mediated Sequelae Of InfectionImmunoglobulin FunctionImmunopathology Of Infectious DiseasesDisease Onset TimingHumoral Immunity ImpairmentImmunoglobulin G ResponsesImmunoglobulin M SeroprevalenceImmunoglobulin ResponsesSars-cov-2 InfectionViral Antigen Recognition
Abstract Long-term antibody responses and neutralizing activities following SARS-CoV-2 infections have not yet been elucidated. We quantified immunoglobulin M (IgM) and G (IgG) antibodies recognizing the SARS-CoV-2 receptor-binding domain (RBD) of the spike (S) or the nucleocapsid (N) protein, and neutralizing antibodies during a period of six months following COVID-19 disease onset in 349 symptomatic COVID-19 patients, which were among the first world-wide being infected. The positivity rate and magnitude of IgM-S and IgG-N responses increased rapidly. High levels of IgM-S/N and IgG-S/N at 2-3 weeks after disease onset were associated with virus control and IgG-S titers correlated closely with the capacity to neutralize SARS-CoV-2. While specific IgM-S/N became undetectable 12 weeks after disease onset in most patients, IgG-S/N titers showed an intermediate contraction phase, but stabilized at relatively high levels over the six months observation period. At late time points the positivity rates for binding and neutralizing SARS-CoV-2-specific antibodies was still over 70%. Taken together, our data indicate sustained humoral immunity in recovered patients who suffer from symptomatic COVID-19, suggesting prolonged immunity.
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