Home > Research > Publications & Outputs > Igg seroconversion and pathophysiology in sever...

Links

Text available via DOI:

View graph of relations

Igg seroconversion and pathophysiology in severe acute respiratory syndrome coronavirus 2 infection

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published
  • Henry M. Staines
  • Daniela E. Kirwan
  • David J. Clark
  • 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
  • Grant A. Kay
  • Kesja Klekotko
  • Zawditu Lewis
  • Derek C. Macallan
  • Josephine Mensah-Kane
  • 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
Close
<mark>Journal publication date</mark>31/01/2021
<mark>Journal</mark>Emerging Infectious Diseases
Issue number1
Volume27
Number of pages7
Pages (from-to)85-91
Publication StatusPublished
Early online date30/11/20
<mark>Original language</mark>English

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.