Correlation of humoral immune responses to different SARS-CoV-2 antigens with virus neutralizing antibodies and symptomatic severity in a German COVID-19 cohort

Emerg Microbes Infect. 2021 Dec;10(1):774-781. doi: 10.1080/22221751.2021.1913973.

Abstract

Monitoring the humoral protective immune response and its durability after SARS-CoV-2 infections is essential for risk assessment of reinfections, the improvement of diagnostic methods and the evaluation of vaccine trials. We have analyzed neutralizing antibodies and IgG responses specific to different antigens, including the inactivated whole-virion of SARS-CoV-2, the spike subunit 1 protein and its receptor binding domain, as well as the nucleocapsid protein. We show the dynamic developments of the responses from the early convalescent stages up to 9 months post symptoms onset in follow-up samples from 57 COVID-19 patients with varying clinical severity. By correlating antibody signals to neutralizing titres, valid diagnostic markers for the estimation of neutralizing protection could be identified.

Keywords: COVID-19; RBD-ELISA; S1-ELISA; humoral immunity; inactivated SARS-CoV-2; neutralizing antibodies; nucleocapsid-ELISA.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Neutralizing / blood*
  • Antibodies, Viral / blood*
  • Antigens, Viral / immunology*
  • COVID-19 / immunology*
  • COVID-19 / virology*
  • Child
  • Cohort Studies
  • Coronavirus Nucleocapsid Proteins / immunology
  • Female
  • Follow-Up Studies
  • Germany
  • Humans
  • Immunity, Humoral*
  • Immunoglobulin G / blood
  • Male
  • Middle Aged
  • Pandemics
  • Phosphoproteins / immunology
  • SARS-CoV-2 / immunology*
  • Severity of Illness Index
  • Spike Glycoprotein, Coronavirus / immunology
  • Time Factors
  • Virion / immunology
  • Young Adult

Substances

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • Antigens, Viral
  • Coronavirus Nucleocapsid Proteins
  • Immunoglobulin G
  • Phosphoproteins
  • Spike Glycoprotein, Coronavirus
  • nucleocapsid phosphoprotein, SARS-CoV-2
  • spike protein, SARS-CoV-2

Grants and funding

This publication was supported by Saxon State Ministry for Science, Culture and Tourism (grant SaxoCOV) and the European Virus Archive GLOBAL (EVA-GLOBAL) project that has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No 871029.