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

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

Journal

Emerging infectious diseases
ISSN: 1080-6059
Titre abrégé: Emerg Infect Dis
Pays: United States
ID NLM: 9508155

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 2 12 2020
medline: 6 1 2021
entrez: 1 12 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33256890
doi: 10.3201/eid2701.203074
pmc: PMC7774532
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0

Banques de données

ClinicalTrials.gov
['NCT04351646']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P019978/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P019978/2
Pays : United Kingdom

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Auteurs

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Classifications MeSH