IgG Seroconversion and Pathophysiology in Severe Acute Respiratory Syndrome Coronavirus 2 Infection

Emerg Infect Dis. 2021 Jan;27(1):85-91. doi: 10.3201/eid2701.203074. Epub 2020 Nov 30.

Abstract

We investigated the dynamics of seroconversion in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. During March 29-May 22, 2020, we collected serum samples and associated clinical data from 177 persons in London, UK, who had SARS-CoV-2 infection. We measured IgG against SARS-CoV-2 and compared antibody levels with patient outcomes, demographic information, and laboratory characteristics. We found that 2.0%-8.5% of persons did not seroconvert 3-6 weeks after infection. Persons who seroconverted were older, were more likely to have concurrent conditions, and had higher levels of inflammatory markers. Non-White persons had higher antibody concentrations than those who identified as White; these concentrations did not decline during follow-up. Serologic assay results correlated with disease outcome, race, and other risk factors for severe SARS-CoV-2 infection. Serologic assays can be used in surveillance to clarify the duration and protective nature of humoral responses to SARS-CoV-2 infection.

Trial registration: ClinicalTrials.gov NCT04351646.

Keywords: 2019 novel coronavirus disease; COVID-19; SARS-CoV-2; United Kingdom; antibodies; antibody responses; coronavirus; coronavirus disease; diagnostics; immunology; respiratory infections; serology; severe acute respiratory syndrome coronavirus 2; viruses; zoonoses.

MeSH terms

  • Adult
  • Aged
  • Antibodies, Viral / blood
  • COVID-19 / blood*
  • COVID-19 / immunology*
  • COVID-19 / physiopathology
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Humans
  • Immunoglobulin G / blood*
  • Male
  • Middle Aged
  • Reverse Transcriptase Polymerase Chain Reaction
  • SARS-CoV-2*
  • Seroconversion*

Substances

  • Antibodies, Viral
  • Immunoglobulin G

Associated data

  • ClinicalTrials.gov/NCT04351646