Association between IgG responses against the nucleocapsid proteins of alphacoronaviruses and COVID-19 severity

Front Immunol. 2022 Sep 7:13:889836. doi: 10.3389/fimmu.2022.889836. eCollection 2022.

Abstract

Understanding immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is crucial to contain the COVID-19 pandemic. Using a multiplex approach, serum IgG responses against the whole SARS-CoV-2 proteome and the nucleocapsid proteins of endemic human coronaviruses (HCoVs) were measured in SARS-CoV-2-infected donors and healthy controls. COVID-19 severity strongly correlated with IgG responses against the nucleocapsid (N) of SARS-CoV-2 and possibly with the number of viral antigens targeted. Furthermore, a strong correlation between COVID-19 severity and serum responses against N of endemic alpha- but not betacoronaviruses was detected. This correlation was neither caused by cross-reactivity of antibodies, nor by a general boosting effect of SARS-CoV-2 infection on pre-existing humoral immunity. These findings raise the prospect of a potential disease progression marker for COVID-19 severity that allows for early stratification of infected individuals.

Keywords: COVID-19; SARS-CoV-2; coronavirus; multiplex serology; nucleocapsid protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alphacoronavirus*
  • Antibodies, Viral
  • Antigens, Viral
  • COVID-19*
  • Humans
  • Immunoglobulin G
  • Nucleocapsid Proteins
  • Pandemics
  • Proteome
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • Immunoglobulin G
  • Nucleocapsid Proteins
  • Proteome
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2