Emerging Infectious Diseases (Jan 2021)

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

  • Henry M. Staines,
  • Daniela E. Kirwan,
  • David J. Clark,
  • Emily R. Adams,
  • Yolanda Augustin,
  • Rachel L. Byrne,
  • Michael Cocozza,
  • Ana I. Cubas-Atienzar,
  • Luis E. Cuevas,
  • Martina Cusinato,
  • Benedict M.O. Davies,
  • Mark Davis,
  • Paul Davis,
  • Annelyse Duvoix,
  • Nicholas M. Eckersley,
  • Daniel Forton,
  • Alice J. Fraser,
  • Gala Garrod,
  • Linda Hadcocks,
  • Qinxue Hu,
  • Michael Johnson,
  • Grant A. Kay,
  • Kesja Klekotko,
  • Zawditu Lewis,
  • Derek C. Macallan,
  • Josephine Mensah-Kane,
  • Stefanie Menzies,
  • Irene Monahan,
  • Catherine M. Moore,
  • Gerhard Nebe-von-Caron,
  • Sophie I. Owen,
  • Chris Sainter,
  • Amadou A. Sall,
  • James Schouten,
  • Christopher T. Williams,
  • John Wilkins,
  • Kevin Woolston,
  • Joseph R.A. Fitchett,
  • Sanjeev Krishna,
  • Tim Planche

DOI
https://doi.org/10.3201/eid2701.203074
Journal volume & issue
Vol. 27, no. 1
pp. 85 – 91

Abstract

Read online

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.

Keywords